Infections with viruses of the family PARAMYXOVIRIDAE. This includes MORBILLIVIRUS INFECTIONS; RESPIROVIRUS INFECTIONS; PNEUMOVIRUS INFECTIONS; HENIPAVIRUS INFECTIONS; AVULAVIRUS INFECTIONS; and RUBULAVIRUS INFECTIONS.
A family of spherical viruses, of the order MONONEGAVIRALES, somewhat larger than the orthomyxoviruses, and containing single-stranded RNA. Subfamilies include PARAMYXOVIRINAE and PNEUMOVIRINAE.
A subfamily of PARAMYXOVIRIDAE. Genera include RUBULAVIRUS; RESPIROVIRUS; MORBILLIVIRUS; HENIPAVIRUS; and AVULAVIRUS.
A species of HENIPAVIRUS, closely related to HENDRA VIRUS, which emerged in Peninsular Malaysia in 1998. It causes a severe febrile VIRAL ENCEPHALITIS in humans and also encephalitis and RESPIRATORY TRACT INFECTIONS in pigs. Fruit bats (PTEROPUS) are the natural host.
A genus of the family PARAMYXOVIRIDAE (subfamily PARAMYXOVIRINAE) where the virions of most members have hemagglutinin but not neuraminidase activity. All members produce both cytoplasmic and intranuclear inclusion bodies. MEASLES VIRUS is the type species.
Infections with viruses of the genus HENIPAVIRUS, family PARAMYXOVIRIDAE.
A genus in the subfamily PARAMYXOVIRINAE, family PARAMYXOVIRIDAE. It contains species that infect and cause potentially fatal disease in a number of host species, including humans.
A genus of the subfamily PNEUMOVIRINAE, containing two members: Turkey rhinotracheitis virus and a human Metapneumovirus. Virions lack HEMAGGLUTININ and NEURAMINIDASE.
A genus in the subfamily PARAMYXOVIRINAE, family PARAMYXOVIRIDAE, causing disease in domestic fowl. There are many species, the most well-known being avian paramyxovirus 1 (NEWCASTLE DISEASE VIRUS).
An order comprising four families of eukaryotic viruses possessing linear, non-segmented, negative-strand RNA genomes. The families are BORNAVIRIDAE; FILOVIRIDAE; PARAMYXOVIRIDAE; and RHABDOVIRIDAE.
A species of HENIPAVIRUS first identified in Australia in 1994 in HORSES and transmitted to humans. The natural host appears to be fruit bats (PTEROPUS).
A genus of the family PARAMYXOVIRIDAE (subfamily PNEUMOVIRINAE) where the human and bovine virions have neither hemagglutinin nor neuraminidase activity. RESPIRATORY SYNCYTIAL VIRUS, HUMAN is the type species.
The type species of RUBULAVIRUS that causes an acute infectious disease in humans, affecting mainly children. Transmission occurs by droplet infection.
A genus of the family PARAMYXOVIRIDAE (subfamily PARAMYXOVIRINAE) where all the species have hemagglutinin and neuraminidase activities but lack a C protein. MUMPS VIRUS is the type species.
A genus of the family PARAMYXOVIRIDAE (subfamily PARAMYXOVIRINAE) where all the virions have both HEMAGGLUTININ and NEURAMINIDASE activities and encode a non-structural C protein. SENDAI VIRUS is the type species.
Infections with viruses of the genus RESPIROVIRUS, family PARAMYXOVIRIDAE. Host cell infection occurs by adsorption, via HEMAGGLUTININ, to the cell surface.
Infections with viruses of the genus PNEUMOVIRUS, family PARAMYXOVIRIDAE. This includes RESPIRATORY SYNCYTIAL VIRUS INFECTIONS, an important cause of respiratory disease in humans.
Proteins, usually glycoproteins, found in the viral envelopes of a variety of viruses. They promote cell membrane fusion and thereby may function in the uptake of the virus by cells.
A family of bullet-shaped viruses of the order MONONEGAVIRALES, infecting vertebrates, arthropods, protozoa, and plants. Genera include VESICULOVIRUS; LYSSAVIRUS; EPHEMEROVIRUS; NOVIRHABDOVIRUS; Cytorhabdovirus; and Nucleorhabdovirus.
The type species of RESPIROVIRUS in the subfamily PARAMYXOVIRINAE. It is the murine version of HUMAN PARAINFLUENZA VIRUS 1, distinguished by host range.
A species of RUBULAVIRUS associated particularly with acute laryngotracheitis (CROUP) in children aged 6 months to 3 years.
The most well known avian paramyxovirus in the genus AVULAVIRUS and the cause of a highly infectious pneumoencephalitis in fowl. It is also reported to cause CONJUNCTIVITIS in humans. Transmission is by droplet inhalation or ingestion of contaminated water or food.
A species of MORBILLIVIRUS causing distemper in dogs, wolves, foxes, raccoons, and ferrets. Pinnipeds have also been known to contract Canine distemper virus from contact with domestic dogs.
Order of mammals whose members are adapted for flight. It includes bats, flying foxes, and fruit bats.
The type species of MORBILLIVIRUS and the cause of the highly infectious human disease MEASLES, which affects mostly children.
Proteins found in any species of virus.
A CELL LINE derived from the kidney of the African green (vervet) monkey, (CERCOPITHECUS AETHIOPS) used primarily in virus replication studies and plaque assays.
An acute febrile, contagious, viral disease of birds caused by an AVULAVIRUS called NEWCASTLE DISEASE VIRUS. It is characterized by respiratory and nervous symptoms in fowl and is transmissible to man causing a severe, but transient conjunctivitis.
Viral proteins found in either the NUCLEOCAPSID or the viral core (VIRAL CORE PROTEINS).
The complete genetic complement contained in a DNA or RNA molecule in a virus.
A group of viruses in the PNEUMOVIRUS genus causing respiratory infections in various mammals. Humans and cattle are most affected but infections in goats and sheep have also been reported.
A species of CERCOPITHECUS containing three subspecies: C. tantalus, C. pygerythrus, and C. sabeus. They are found in the forests and savannah of Africa. The African green monkey (C. pygerythrus) is the natural host of SIMIAN IMMUNODEFICIENCY VIRUS and is used in AIDS research.
Pneumovirus infections caused by the RESPIRATORY SYNCYTIAL VIRUSES. Humans and cattle are most affected but infections in goats and sheep have been reported.
The relationships of groups of organisms as reflected by their genetic makeup.
Descriptions of specific amino acid, carbohydrate, or nucleotide sequences which have appeared in the published literature and/or are deposited in and maintained by databanks such as GENBANK, European Molecular Biology Laboratory (EMBL), National Biomedical Research Foundation (NBRF), or other sequence repositories.
Ribonucleic acid that makes up the genetic material of viruses.
Established cell cultures that have the potential to propagate indefinitely.
The order of amino acids as they occur in a polypeptide chain. This is referred to as the primary structure of proteins. It is of fundamental importance in determining PROTEIN CONFORMATION.
The process of intracellular viral multiplication, consisting of the synthesis of PROTEINS; NUCLEIC ACIDS; and sometimes LIPIDS, and their assembly into a new infectious particle.
Immunoglobulins produced in response to VIRAL ANTIGENS.
The sequence of PURINES and PYRIMIDINES in nucleic acids and polynucleotides. It is also called nucleotide sequence.
Inflammation of the lung parenchyma that is caused by a viral infection.
Infection of the lung often accompanied by inflammation.
Inflammation of the lung parenchyma that is caused by bacterial infections.
A species of RESPIROVIRUS also called hemadsorption virus 2 (HA2), which causes laryngotracheitis in humans, especially children.
An acute viral infection in humans involving the respiratory tract. It is marked by inflammation of the NASAL MUCOSA; the PHARYNX; and conjunctiva, and by headache and severe, often generalized, myalgia.
A subtype of INFLUENZA A VIRUS with the surface proteins hemagglutinin 1 and neuraminidase 1. The H1N1 subtype was responsible for the Spanish flu pandemic of 1918.

Cell-mediated immune responses in cattle vaccinated with a vaccinia virus recombinant expressing the nucleocapsid protein of rinderpest virus. (1/544)

Rinderpest virus (RPV) is a member of the genus Morbillivirus in the family Paramyxoviridae which causes an acute and often fatal disease in large ruminants. To examine the immune response to the virus nucleocapsid (N) protein, a recombinant vaccinia virus expressing RPV nucleocapsid protein (rVV-RPV-N) was used to vaccinate cattle. The recombinant vaccine induced low levels of non-neutralizing anti-N antibodies. RPV-specific cell-mediated immunity induced by the recombinant was assessed by measuring both the lymphocyte proliferation and cytotoxic T-lymphocyte responses. The protective immune response was examined by challenging the vaccinated cattle with either a highly virulent (Saudi 1/81) or a mild (Kenya/eland/96) strain of the virus. The vaccinated cattle were not protected against challenge with the virulent RPV strain, except they showed a slight delay in the onset of disease when compared with the unvaccinated controls. In cattle challenged with the mild strain, apart from a transient fever, no clinical signs of rinderpest infection were seen in the vaccinated cattle. One out of two control cattle showed a similar response but the other died from classic rinderpest disease. Virus-neutralizing antibodies were induced more quickly following challenge with the mild strain in vaccinated cattle compared to the control animals. These data suggested that the cell-mediated immunity induced by rVV-RPV-N could stimulate the rapid production of neutralizing antibodies following RPV challenge but this response was not sufficient to protect against challenge with a virulent strain of the virus. Protection was seen in one of three animals challenged with a mild strain of the virus; however, a greater number of animals would need to be tested to estimate the significance of the protection afforded by the N protein.  (+info)

Parainfluenza virus infection among adults hospitalized for lower respiratory tract infection. (2/544)

To better define the contribution of human parainfluenza viruses (HPIVs) to lower respiratory tract infection in adults, we tested acute- and convalescent-phase serum specimens from hospitalized adults participating in a population-based prospective study of lower respiratory tract infection during 1991-1992. We tested all available specimens from the epidemic seasons for each virus and approximately 300 randomly selected specimens from the corresponding off-seasons for antibodies to HPIV-1, HPIV-2, or HPIV-3. During the respective epidemic season, HPIV-1 infection was detected in 18 (2.5%) of 721 and HPIV-3 infection in 22 (3.1%) of 705 patients with lower respiratory tract infection. Only 2 (0.2%) of 1,057 patients tested positive for HPIV-2 infection. No HPIV-1 infections and only 2 (0.7% of 281 patients tested) HPIV-3 infections were detected during the off-seasons. HPIV-1 and HPIV-3 were among the four most frequently identified infections associated with lower respiratory tract infection during their respective outbreak seasons.  (+info)

Ovalbumin sensitization changes the inflammatory response to subsequent parainfluenza infection. Eosinophils mediate airway hyperresponsiveness, m(2) muscarinic receptor dysfunction, and antiviral effects. (3/544)

Asthma exacerbations, many of which are virus induced, are associated with airway eosinophilia. This may reflect altered inflammatory response to viruses in atopic individuals. Inhibitory M(2) muscarinic receptors (M(2)Rs) on the airway parasympathetic nerves limit acetylcholine release. Both viral infection and inhalational antigen challenge cause M(2)R dysfunction, leading to airway hyperresponsiveness. In antigen-challenged, but not virus-infected guinea pigs, M(2)R dysfunction is due to blockade of the receptors by the endogenous antagonist eosinophil major basic protein (MBP). We hypothesized that sensitization to a nonviral antigen before viral infection alters the inflammatory response to viral infection, so that M(2)R dysfunction and hyperreactivity are eosinophil mediated. Guinea pigs were sensitized to ovalbumin intraperitoneally, and 3 wk later were infected with parainfluenza. In sensitized, but not in nonsensitized animals, virus-induced hyperresponsiveness and M(2)R dysfunction were blocked by depletion of eosinophils with antibody to interleukin (IL)-5 or treatment with antibody to MBP. An additional and unexpected finding was that sensitization to ovalbumin caused a marked (80%) reduction in the viral content of the lungs. This was reversed by the antibody to IL-5, implicating a role for eosinophils in viral immunity.  (+info)

Nipah viral encephalitis or Japanese encephalitis? MR findings in a new zoonotic disease. (4/544)

BACKGROUND AND PURPOSE: An epidemic of suspected Japanese encephalitis occurred in Malaysia in 1998-1999 among pig farmers. In neighboring Singapore, an outbreak occurred among pig slaughterhouse workers. It was subsequently established that the causative agent in the outbreak was not the Japanese encephalitis virus but a previously unknown Hendra-like paramyxovirus named Nipah virus. METHODS: The brain MR images of eight patients with Nipah virus infection were reviewed. All patients tested negative for acute Japanese encephalitis virus. Seven patients had contrast-enhanced studies and six had diffusion-weighted examinations. RESULTS: All patients had multiple small bilateral foci of T2 prolongation within the subcortical and deep white matter. The periventricular region and corpus callosum were also involved. In addition to white matter disease, five patients had cortical lesions, three had brain stem involvement, and a single thalamic lesion was detected in one patient. All lesions were less than 1 cm in maximum diameter. In five patients, diffusion-weighted images showed increased signal. Four patients had leptomeningeal enhancement and four had enhancement of parenchymal lesions. CONCLUSION: The brain MR findings in patients infected with the newly discovered Nipah paramyxovirus are different from those of patients with Japanese encephalitis. In a zoonotic epidemic, this striking difference in the appearance and distribution of lesions is useful in differentiating these diseases. Diffusion-weighted imaging was advantageous in increasing lesion conspicuity.  (+info)

Clinical features of Nipah virus encephalitis among pig farmers in Malaysia. (5/544)

BACKGROUND: Between September 1998 and June 1999, there was an outbreak of severe viral encephalitis due to Nipah virus, a newly discovered paramyxovirus, in Malaysia. METHODS: We studied the clinical features of the patients with Nipah virus encephalitis who were admitted to a medical center in Kuala Lumpur. The case definition was based on epidemiologic, clinical, cerebrospinal fluid, and neuroimaging findings. RESULTS: Ninety-four patients with Nipah virus infection were seen from February to June 1999 (mean age, 37 years; ratio of male patients to female patients, 4.5 to 1). Ninety-three percent had had direct contact with pigs, usually in the two weeks before the onset of illness, suggesting that there was direct viral transmission from pigs to humans and a short incubation period. The main presenting features were fever, headache, dizziness, and vomiting. Fifty-two patients (55 percent) had a reduced level of consciousness and prominent brain-stem dysfunction. Distinctive clinical signs included segmental myoclonus, areflexia and hypotonia, hypertension, and tachycardia and thus suggest the involvement of the brain stem and the upper cervical spinal cord. The initial cerebrospinal fluid findings were abnormal in 75 percent of patients. Antibodies against Hendra virus were detected in serum or cerebrospinal fluid in 76 percent of 83 patients tested. Thirty patients (32 percent) died after rapid deterioration in their condition. An abnormal doll's-eye reflex and tachycardia were factors associated with a poor prognosis. Death was probably due to severe brain-stem involvement. Neurologic relapse occurred after initially mild disease in three patients. Fifty patients (53 percent) recovered fully, and 14 (15 percent) had persistent neurologic deficits. CONCLUSIONS: Nipah virus causes a severe, rapidly progressive encephalitis with a high mortality rate and features that suggest involvement of the brain stem. The infection is associated with recent contact with pigs.  (+info)

Case-control study of risk factors for human infection with a new zoonotic paramyxovirus, Nipah virus, during a 1998-1999 outbreak of severe encephalitis in Malaysia. (6/544)

An outbreak of encephalitis affecting 265 patients (105 fatally) occurred during 1998-1999 in Malaysia and was linked to a new paramyxovirus, Nipah, that infected pigs, humans, dogs, and cats. Most patients were pig farmers. Clinically undetected Nipah infection was noted in 10 (6%) of 166 community-farm controls (persons from farms without reported encephalitis patients) and 20 (11%) of 178 case-farm controls (persons from farms with encephalitis patients). Case patients (persons with Nipah infection) were more likely than community-farm controls to report increased numbers of sick/dying pigs on the farm (59% vs. 24%, P=.001) and were more likely than case-farm controls to perform activities requiring direct contact with pigs (86% vs. 50%, P=.005). Only 8% of case patients reported no contact with pigs. The outbreak stopped after pigs in the affected areas were slaughtered and buried. Direct, close contact with pigs was the primary source of human Nipah infection, but other sources, such as infected dogs and cats, cannot be excluded.  (+info)

Risk factors for Nipah virus infection among abattoir workers in Singapore. (7/544)

During 10-19 March 1999, 11 workers in 1 of 2 Singaporean abattoirs developed Nipah-virus associated encephalitis or pneumonia, resulting in 1 fatality. A case-control study was conducted to determine occupational risk factors for infection. Case patients were abattoir A workers who had anti-Nipah IgM antibodies; control subjects were randomly selected abattoir A workers who tested negative for anti-Nipah IgM. All 13 case patients versus 26 (63%) of 41 control subjects reported contact with live pigs (P=.01). Swine importation from Malaysian states concurrently experiencing a Nipah virus outbreak was banned on 3 March 1999; on 19 March 1999, importation of Malaysian pigs was banned, and abattoirs were closed. No unusual illnesses among pigs processed during February-March were reported. Contact with live pigs appeared to be the most important risk factor for human Nipah virus infection. Direct contact with live, potentially infected pigs should be minimized to prevent transmission of this potentially fatal zoonosis to humans.  (+info)

Nipah virus: a recently emergent deadly paramyxovirus. (8/544)

A paramyxovirus virus termed Nipah virus has been identified as the etiologic agent of an outbreak of severe encephalitis in people with close contact exposure to pigs in Malaysia and Singapore. The outbreak was first noted in late September 1998 and by mid-June 1999, more than 265 encephalitis cases, including 105 deaths, had been reported in Malaysia, and 11 cases of encephalitis or respiratory illness with one death had been reported in Singapore. Electron microscopic, serologic, and genetic studies indicate that this virus belongs to the family Paramyxoviridae and is most closely related to the recently discovered Hendra virus. We suggest that these two viruses are representative of a new genus within the family Paramyxoviridae. Like Hendra virus, Nipah virus is unusual among the paramyxoviruses in its ability to infect and cause potentially fatal disease in a number of host species, including humans.  (+info)

Paramyxoviridae is a family of viruses that includes several important pathogens causing respiratory infections in humans and animals. According to the medical perspective, Paramyxoviridae infections refer to the diseases caused by these viruses.

Some notable human paramyxovirus infections include:

1. Respiratory Syncytial Virus (RSV) Infection: RSV is a common cause of respiratory tract infections, particularly in young children and older adults. It can lead to bronchiolitis and pneumonia, especially in infants and patients with compromised immune systems.
2. Measles (Rubeola): Measles is a highly contagious viral disease characterized by fever, cough, coryza (runny nose), conjunctivitis, and a maculopapular rash. It can lead to severe complications such as pneumonia, encephalitis, and even death, particularly in malnourished children and individuals with weakened immune systems.
3. Parainfluenza Virus Infection: Parainfluenza viruses are responsible for upper and lower respiratory tract infections, including croup, bronchitis, and pneumonia. They mainly affect young children but can also infect adults, causing mild to severe illnesses.
4. Mumps: Mumps is a contagious viral infection that primarily affects the salivary glands, causing painful swelling. It can lead to complications such as meningitis, encephalitis, deafness, and orchitis (inflammation of the testicles) in rare cases.
5. Human Metapneumovirus (HMPV) Infection: HMPV is a respiratory virus that can cause upper and lower respiratory tract infections, similar to RSV and parainfluenza viruses. It mainly affects young children and older adults, leading to bronchitis, pneumonia, and exacerbations of chronic lung diseases.

Prevention strategies for Paramyxoviridae infections include vaccination programs, practicing good personal hygiene, and implementing infection control measures in healthcare settings.

Paramyxoviridae is a family of negative-sense, single-stranded RNA viruses that include several medically important pathogens. These viruses are characterized by their enveloped particles and helical symmetry. The paramyxoviruses can cause respiratory infections, neurological disorders, and other systemic diseases in humans, animals, and birds.

Some notable members of the Paramyxoviridae family include:

* Human respirovirus (also known as human parainfluenza virus): causes upper and lower respiratory tract infections in children and adults.
* Human orthopneumovirus (also known as respiratory syncytial virus, or RSV): a major cause of bronchiolitis and pneumonia in infants and young children.
* Measles morbillivirus: causes measles, a highly contagious viral disease characterized by fever, rash, and cough.
* Mumps virus: causes mumps, an acute infectious disease that primarily affects the salivary glands.
* Hendra virus and Nipah virus: zoonotic paramyxoviruses that can cause severe respiratory and neurological disease in humans and animals.

Effective vaccines are available for some paramyxoviruses, such as measles and mumps, but there are currently no approved vaccines for others, such as RSV and Nipah virus. Antiviral therapies are also limited, with only a few options available for the treatment of severe paramyxovirus infections.

Paramyxovirinae is a subfamily of viruses in the family Paramyxoviridae, order Mononegavirales. These viruses are enveloped, negative-sense, single-stranded RNA viruses that cause various diseases in animals and humans. The subfamily includes several important human pathogens such as:

1. Respiratory syncytial virus (RSV): A major cause of respiratory tract infections in infants, young children, and older adults.
2. Human metapneumovirus (HMPV): Another common cause of respiratory illness, particularly in children.
3. Parainfluenza viruses (PIVs): Responsible for upper and lower respiratory tract infections, including croup, bronchitis, and pneumonia.
4. Mumps virus: Causes the infectious disease mumps, characterized by swelling of the salivary glands.
5. Measles virus: A highly contagious virus that causes measles, a serious respiratory illness with characteristic rash.
6. Hendra virus and Nipah virus: Zoonotic viruses that can cause severe respiratory and neurological diseases in humans and animals.

These viruses share common structural and genetic features, such as an enveloped virion with a helical nucleocapsid, and a genome consisting of non-segmented, negative-sense single-stranded RNA. They also utilize similar replication strategies and have related gene arrangements.

Nipah virus (NiV) is a zoonotic virus (it is transmitted from animals to humans) that causes severe illness in both humans and animals. It was first identified during an outbreak of disease in pigs and people in Malaysia and Singapore in 1998-1999.

The natural host of the virus are fruit bats of the Pteropodidae Family, Pteropus genus. Transmission to humans may occur through direct contact with infected bats or consumption of date palm sap contaminated by excretions or secretions from infected bats. Human-to-human transmission is also possible through close contact with people's secretions and excretions.

Infection with NiV can lead to a range of clinical presentations, from asymptomatic infection to acute respiratory illness and severe encephalitis (inflammation of the brain). The case fatality rate is estimated to be about 40-75% in humans. There is no vaccine available for either humans or animals. Prevention strategies include avoiding consumption of raw date palm sap, wearing protective clothing while handling infected animals or their contaminated materials, and practicing good hygiene.

Morbillivirus is a genus of viruses in the family Paramyxoviridae, order Mononegavirales. It includes several important human and animal pathogens that cause diseases with significant morbidity and mortality. The most well-known member of this genus is Measles virus (MV), which causes measles in humans, a highly contagious disease characterized by fever, rash, cough, and conjunctivitis.

Other important Morbilliviruses include:

* Rinderpest virus (RPV): This virus caused rinderpest, a severe disease in cattle and other cloven-hoofed animals, which was eradicated in 2011 through a global vaccination campaign.
* Canine Distemper Virus (CDV): A pathogen that affects dogs, wild canids, and several other mammalian species, causing a systemic disease with respiratory, gastrointestinal, and neurological symptoms.
* Phocine Distemper Virus (PDV) and Porpoise Morbillivirus (PMV): These viruses affect marine mammals, such as seals and porpoises, causing mass mortality events in their populations.

Morbilliviruses are enveloped, negative-sense, single-stranded RNA viruses with a genome size of approximately 15-16 kilobases. They have a pleomorphic shape and can vary in diameter from 150 to 750 nanometers. The viral envelope contains two glycoproteins: the hemagglutinin (H) protein, which mediates attachment to host cells, and the fusion (F) protein, which facilitates membrane fusion and viral entry.

Transmission of Morbilliviruses typically occurs through respiratory droplets or direct contact with infected individuals or animals. The viruses can cause acute infections with high fatality rates, particularly in naïve populations that lack immunity due to insufficient vaccination coverage or the absence of previous exposure.

In summary, Morbillivirus is a genus of viruses in the family Paramyxoviridae that includes several important human and animal pathogens causing acute respiratory infections with high fatality rates. Transmission occurs through respiratory droplets or direct contact, and vaccination plays a crucial role in preventing outbreaks and controlling disease spread.

Henipavirus infections are caused by two paramyxoviruses, Hendra virus and Nipah virus. These viruses can cause severe illness in both humans and animals, particularly horses and pigs.

The natural hosts for these viruses are fruit bats (Pteropus spp.), also known as flying foxes. Transmission to humans can occur through direct contact with infected animals or their bodily fluids, consumption of contaminated food or drink, or through exposure to an environment contaminated with the virus.

Infection with Hendra virus can cause respiratory and neurological symptoms in humans, with a high fatality rate. Nipah virus infection can cause respiratory illness, fever, headache, dizziness, and altered consciousness, which can progress to encephalitis and coma. The case fatality rate for Nipah virus infection is estimated to be around 40-75%.

There are no specific treatments or vaccines available for henipavirus infections, and prevention efforts focus on reducing exposure to the viruses through public health measures such as avoiding contact with infected animals and their bodily fluids, practicing good hygiene and food safety, and implementing appropriate infection control practices.

Henipavirus is a genus of the Paramyxoviridae family, which consists of enveloped, negative-sense, single-stranded RNA viruses. This genus includes two major species that are known to cause severe disease in humans: Nipah virus and Hendra virus. These viruses are primarily hosted by fruit bats (Pteropus spp.), but they can also infect other animals such as pigs, horses, and cats, and can be transmitted to humans through close contact with infected animals or their secretions. Henipaviruses are classified as biosafety level 4 agents due to their high mortality rate and potential for causing severe epidemics. Infection with these viruses can lead to a range of clinical symptoms, including fever, respiratory distress, and encephalitis, which can be fatal in some cases.

Metapneumovirus is a type of virus that can cause respiratory infections in humans and animals. The human metapneumovirus (HMPV) is a leading cause of acute respiratory infection (ARI), particularly in young children, the elderly, and people with weakened immune systems. It is associated with a wide range of clinical manifestations, ranging from mild upper respiratory symptoms to severe bronchiolitis and pneumonia.

HMPV is an enveloped, single-stranded RNA virus that belongs to the Pneumoviridae family, subfamily Pneumovirinae, and genus Metapneumovirus. It was first identified in 2001, although it is believed to have been circulating in humans for at least 50 years before its discovery. HMPV is transmitted through respiratory droplets and direct contact with infected individuals or contaminated surfaces.

The incubation period of HMPV ranges from 3 to 6 days, after which symptoms such as cough, fever, nasal congestion, sore throat, and difficulty breathing may appear. In severe cases, HMPV can lead to bronchitis, bronchiolitis, or pneumonia, requiring hospitalization, especially in high-risk populations. Currently, there is no specific antiviral treatment for HMPV infections, and management typically involves supportive care, such as oxygen therapy, hydration, and respiratory support if necessary. Prevention measures include good hand hygiene, wearing masks, and avoiding close contact with infected individuals.

Avulavirus is a genus of viruses in the family Paramyxoviridae, order Mononegavirales. Avulaviruses are enveloped, negative-sense, single-stranded RNA viruses that primarily infect birds, causing various clinical manifestations such as respiratory, digestive, and reproductive diseases. Some avulaviruses have been associated with sporadic human infections, usually resulting in mild or asymptomatic illnesses. The most well-known avulavirus is the Newcastle disease virus (NDV), which can cause severe disease in birds and poses a significant threat to the poultry industry worldwide.

Mononegavirales is an order of viruses that includes several families of negative-strand RNA viruses, such as Paramyxoviridae, Rhabdoviridae, and Filoviridae. These viruses are characterized by their single, non-segmented strand of RNA that is negative-sense, meaning it cannot be directly translated into protein by the host cell's machinery. Instead, a complementary positive-sense RNA must first be synthesized before protein production can occur.

The order Mononegavirales includes many important human and animal pathogens, such as measles virus, mumps virus, respiratory syncytial virus (RSV), rabies virus, Ebola virus, and Marburg virus. These viruses can cause a range of diseases, from mild respiratory infections to severe hemorrhagic fevers.

The virions of Mononegavirales are typically enveloped, with a helical capsid that surrounds the RNA genome. The genome is usually around 10-15 kilobases in length and encodes several proteins, including an RNA-dependent RNA polymerase that is responsible for replicating and transcribing the viral RNA.

Mononegavirales viruses are transmitted through various routes, including respiratory droplets, bodily fluids, and contact with infected animals or fomites. Prevention and control measures include vaccination, personal protective equipment (PPE), and infection control practices.

Hendra virus (HeV) is an enveloped, negative-sense, single-stranded RNA virus that belongs to the genus Henipavirus in the family Paramyxoviridae. It was initially identified in 1994 during an outbreak of a mysterious disease affecting horses and humans in Hendra, a suburb of Brisbane, Australia. The natural host of this virus is the fruit bat (Pteropus spp.), also known as flying foxes.

HeV infection can cause severe respiratory and neurological diseases in various mammals, including horses, humans, and other domestic animals. Horses are considered the primary source of human infections, as they get infected after direct or indirect contact with body fluids (e.g., urine, saliva, or nasal discharge) from infected fruit bats. Human cases usually occur through close contact with infected horses or their bodily fluids during veterinary care, slaughtering, or other activities.

The incubation period in humans ranges from 5 to 16 days, followed by the onset of nonspecific influenza-like symptoms such as fever, cough, sore throat, and muscle pain. In severe cases, HeV can cause pneumonia, encephalitis, or both, with a high fatality rate (approximately 57%). No specific treatment or vaccine is currently available for humans; however, ribavirin has shown some efficacy in treating HeV infections in vitro and in animal models. Preventive measures include avoiding contact with infected horses and implementing strict biosecurity practices when handling potentially infected animals.

Pneumovirus is a genus of viruses in the family Pneumoviridae, order Mononegavirales. It includes several species that can cause respiratory infections in humans and animals. The most well-known species that infect humans is Human Respiratory Syncytial Virus (HRSV), which is a major cause of bronchiolitis and pneumonia in young children, the elderly, and immunocompromised individuals. Other human pneumoviruses include Human Metapneumovirus (HMPV) and Avian Metapneumovirus subtype C (AMPV-C). These viruses can cause similar respiratory symptoms, ranging from mild to severe.

Pneumoviruses are enveloped, negative-sense, single-stranded RNA viruses that replicate in the cytoplasm of infected cells. They have a nonsegmented genome and encode several structural proteins, including an attachment protein, fusion protein, matrix protein, and nucleocapsid protein. The virions are typically pleomorphic, with a diameter of 150-250 nm.

Transmission of pneumoviruses occurs through respiratory droplets or direct contact with contaminated surfaces. Preventive measures include good hygiene practices, such as hand washing and covering the mouth and nose when coughing or sneezing. There are currently no vaccines available for human pneumoviruses, but several candidates are in development. Treatment is primarily supportive and may include oxygen therapy, mechanical ventilation, and antiviral medications in severe cases.

The Mumps virus is a single-stranded, negative-sense RNA virus that belongs to the Paramyxoviridae family and Rubulavirus genus. It is the causative agent of mumps, an acute infectious disease characterized by painful swelling of the salivary glands, particularly the parotid glands.

The Mumps virus has a spherical or pleomorphic shape with a diameter of approximately 150-250 nanometers. It is surrounded by a lipid bilayer membrane derived from the host cell, which contains viral glycoproteins that facilitate attachment and entry into host cells.

The M protein, located beneath the envelope, plays a crucial role in virus assembly and budding. The genome of the Mumps virus consists of eight genes encoding nine proteins, including two major structural proteins (nucleocapsid protein and matrix protein) and several non-structural proteins involved in viral replication and pathogenesis.

Transmission of the Mumps virus occurs through respiratory droplets or direct contact with infected saliva. After infection, the incubation period ranges from 12 to 25 days, followed by a prodromal phase characterized by fever, headache, malaise, and muscle pain. The characteristic swelling of the parotid glands usually appears 1-3 days after the onset of symptoms.

Complications of mumps can include meningitis, encephalitis, orchitis, oophoritis, pancreatitis, and deafness. Prevention relies on vaccination with the measles-mumps-rubella (MMR) vaccine, which is highly effective in preventing mumps and its complications.

Rubulavirus is a genus in the family Paramyxoviridae, order Mononegavirales. It includes several viruses that primarily cause respiratory infections in humans and animals. The most well-known rubulaviruses affecting humans are the human parainfluenza viruses (HPIV) 2 and 4, which can cause croup and bronchitis, and mumps virus, which causes mumps. These viruses are typically spread through respiratory droplets and direct contact with infected individuals. They have enveloped, non-segmented, negative-sense RNA genomes.

Respirovirus is not typically used as a formal medical term in modern taxonomy. However, historically, it was used to refer to a genus of viruses within the family Paramyxoviridae, order Mononegavirales. This genus included several important human and animal pathogens that cause respiratory infections.

Human respiroviruses include:
1. Human parainfluenza virus (HPIV) types 1, 2, and 3: These viruses are a common cause of upper and lower respiratory tract infections, such as croup, bronchitis, and pneumonia, particularly in young children.
2. Sendai virus (also known as murine respirovirus): This virus primarily infects rodents but can occasionally cause mild respiratory illness in humans, especially those who work closely with these animals.

The term "respirovirus" is not officially recognized by the International Committee on Taxonomy of Viruses (ICTV) anymore, and these viruses are now classified under different genera within the subfamily Pneumovirinae: Human parainfluenza viruses 1 and 3 belong to the genus Orthorubulavirus, while Human parainfluenza virus 2 is placed in the genus Metapneumovirus.

Respiroviruses are a genus of viruses in the family *Paramyxoviridae* that includes several important human pathogens, such as parainfluenza virus (PIV) types 1, 2, and 3, and human respiratory syncytial virus (HRSV). These viruses are primarily transmitted through respiratory droplets and direct contact with infected individuals.

Respirovirus infections mainly affect the respiratory tract and can cause a range of symptoms, from mild upper respiratory tract illness to severe lower respiratory tract infections. The severity of the disease depends on various factors, including the age and overall health status of the infected individual.

Parainfluenza viruses are a common cause of acute respiratory infections in children, particularly in those under five years old. They can lead to croup, bronchitis, pneumonia, and other respiratory tract complications. In adults, PIV infections are usually less severe but can still cause upper respiratory symptoms, such as the common cold.

Human respiratory syncytial virus is another important respirovirus that primarily affects young children, causing bronchiolitis and pneumonia. Reinfection with HRSV can occur throughout life, although subsequent infections are typically less severe than the initial infection. In older adults and individuals with compromised immune systems, HRSV infections can lead to serious complications, including pneumonia and exacerbation of chronic lung diseases.

Prevention strategies for respirovirus infections include good personal hygiene practices, such as frequent handwashing and covering the mouth and nose when coughing or sneezing. Vaccines are not available for most respiroviruses; however, research is ongoing to develop effective vaccines against these viruses, particularly HRSV.

Pneumovirus infections refer to respiratory illnesses caused by viruses belonging to the Pneumoviridae family, specifically human respirovirus (hRSV) and human metapneumovirus (hMPV). These viruses primarily infect the respiratory tract and can cause a wide range of symptoms, from mild upper respiratory tract infections to severe lower respiratory tract illnesses such as bronchiolitis and pneumonia.

Human respirovirus (hRSV) is a leading cause of bronchiolitis and pneumonia in infants and young children, while human metapneumovirus (hMPV) tends to infect older children and adults, causing similar respiratory symptoms. Both viruses can also cause more severe disease in immunocompromised individuals, the elderly, and those with underlying medical conditions.

Transmission of these viruses typically occurs through close contact with infected individuals or contaminated surfaces, and they are highly contagious. Preventive measures include good hygiene practices, such as frequent handwashing and avoiding close contact with sick individuals. Currently, there are no vaccines available to prevent pneumovirus infections, but antiviral treatments and supportive care can help manage the symptoms and reduce the risk of complications.

Viral fusion proteins are specialized surface proteins found on the envelope of enveloped viruses. These proteins play a crucial role in the viral infection process by mediating the fusion of the viral membrane with the target cell membrane, allowing the viral genetic material to enter the host cell and initiate replication.

The fusion protein is often synthesized as an inactive precursor, which undergoes a series of conformational changes upon interaction with specific receptors on the host cell surface. This results in the exposure of hydrophobic fusion peptides or domains that insert into the target cell membrane, bringing the two membranes into close proximity and facilitating their merger.

A well-known example of a viral fusion protein is the gp120/gp41 complex found on the Human Immunodeficiency Virus (HIV). The gp120 subunit binds to CD4 receptors and chemokine coreceptors on the host cell surface, triggering conformational changes in the gp41 subunit that expose the fusion peptide and enable membrane fusion. Understanding the structure and function of viral fusion proteins is important for developing antiviral strategies and vaccines.

Rhabdoviridae is a family of negative-sense, single-stranded RNA viruses that include several important human and animal pathogens. The name "Rhabdoviridae" comes from the Greek word "rhabdos," meaning rod, which refers to the characteristic bullet shape of these virions.

The family Rhabdoviridae is divided into six genera: Vesiculovirus, Lyssavirus, Ephemerovirus, Novirhabdovirus, Cytorhabdovirus, and Sphericalvirus. The most well-known member of this family is the rabies virus, which belongs to the genus Lyssavirus.

Rhabdoviruses have a simple structure, consisting of an envelope surrounding a helical nucleocapsid that contains the RNA genome. The virions are typically 100-430 nm in length and 45-100 nm in diameter, with a central electron-dense core surrounded by a less dense matrix protein layer.

Rhabdoviruses infect a wide range of hosts, including mammals, birds, fish, reptiles, and insects. They typically cause acute infections characterized by fever, lethargy, and other nonspecific symptoms. In severe cases, rhabdovirus infections can lead to serious neurological disorders, such as encephalitis or meningitis, and can be fatal if left untreated.

Transmission of rhabdoviruses occurs through various routes, depending on the specific virus and host. For example, rabies virus is typically transmitted through the bite of an infected animal, while other rhabdoviruses may be spread through contact with contaminated bodily fluids or aerosols.

Prevention and control measures for rhabdovirus infections depend on the specific virus and host. For example, rabies vaccination is effective in preventing infection in humans and animals, while other rhabdoviruses may be controlled through quarantine measures, insect control, or antiviral therapy.

Sendai virus, also known as murine parainfluenza virus or pneumonia virus of mice, is a species of paramyxovirus that primarily infects rodents. It is an enveloped, negative-sense, single-stranded RNA virus with a nonsegmented genome. The virus is named after the city of Sendai in Japan where it was first isolated in 1952.

Sendai virus is highly contagious and can cause respiratory illness in mice, rats, and other small rodents. It replicates in the respiratory epithelium, leading to inflammation and necrosis of the airways. The virus can also suppress the host's immune response, making infected animals more susceptible to secondary bacterial infections.

In laboratory settings, Sendai virus is sometimes used as a tool for studying viral pathogenesis, immunology, and gene therapy. It has been used as a vector for delivering genes into mammalian cells, including human cells, due to its ability to efficiently infect and transduce a wide range of cell types.

It's important to note that Sendai virus is not known to infect humans or cause disease in humans, and it is not considered a significant public health concern.

Parainfluenza Virus 2, Human (HPIV-2) is a type of respiratory virus that belongs to the family Paramyxoviridae and genus Respirovirus. It is one of the four serotypes of human parainfluenza viruses (HPIVs), which also include HPIV-1, HPIV-3, and HPIV-4.

HPIV-2 primarily infects the upper respiratory tract and causes mild to moderate symptoms similar to those caused by other respiratory viruses. The infection can lead to inflammation of the nose, throat, and voice box (larynx), resulting in a runny nose, sore throat, cough, and hoarseness. In some cases, HPIV-2 can also cause croup, a condition characterized by a barking cough and stridor (high-pitched breathing sounds) due to inflammation of the upper airways.

HPIV-2 is highly contagious and spreads through respiratory droplets produced when an infected person talks, coughs, or sneezes. The virus can also be transmitted by touching contaminated surfaces and then touching the mouth, nose, or eyes. HPIV-2 infections are most common in infants and young children, but people of all ages can become infected.

There is no specific treatment for HPIV-2 infections, and management typically involves supportive care to alleviate symptoms. Preventive measures include good hygiene practices, such as frequent handwashing, covering the mouth and nose when coughing or sneezing, and avoiding close contact with sick individuals. Vaccines are not available for HPIV-2 infections, but research is ongoing to develop effective vaccines against these viruses.

Newcastle disease virus (NDV) is a single-stranded, negative-sense RNA virus that belongs to the genus Avulavirus in the family Paramyxoviridae. It is the causative agent of Newcastle disease, a highly contagious and often fatal viral infection affecting birds and poultry worldwide. The virus can cause various clinical signs, including respiratory distress, neurological disorders, and decreased egg production, depending on the strain's virulence. NDV has zoonotic potential, but human infections are rare and typically result in mild, flu-like symptoms.

Canine distemper virus (CDV) is a single-stranded RNA virus that belongs to the family Paramyxoviridae and causes a contagious and serious disease in dogs and other animals. The virus primarily affects the respiratory, gastrointestinal, and central nervous systems of infected animals.

The symptoms of canine distemper can vary widely depending on the age and immune status of the animal, as well as the strain of the virus. Initial signs may include fever, lethargy, loss of appetite, and discharge from the eyes and nose. As the disease progresses, affected animals may develop vomiting, diarrhea, pneumonia, and neurological symptoms such as seizures, muscle twitching, and paralysis.

Canine distemper is highly contagious and can be spread through direct contact with infected animals or their respiratory secretions. The virus can also be transmitted through contaminated objects such as food bowls, water dishes, and bedding.

Prevention of canine distemper is achieved through vaccination, which is recommended for all dogs as a core vaccine. It is important to keep dogs up-to-date on their vaccinations and to avoid contact with unfamiliar or unvaccinated animals. There is no specific treatment for canine distemper, and therapy is generally supportive, focusing on managing symptoms and preventing complications.

Chiroptera is the scientific order that includes all bat species. Bats are the only mammals capable of sustained flight, and they are distributed worldwide with the exception of extremely cold environments. They vary greatly in size, from the bumblebee bat, which weighs less than a penny, to the giant golden-crowned flying fox, which has a wingspan of up to 6 feet.

Bats play a crucial role in many ecosystems as pollinators and seed dispersers for plants, and they also help control insect populations. Some bat species are nocturnal and use echolocation to navigate and find food, while others are diurnal and rely on their vision. Their diet mainly consists of insects, fruits, nectar, and pollen, although a few species feed on blood or small vertebrates.

Unfortunately, many bat populations face significant threats due to habitat loss, disease, and wind turbine collisions, leading to declining numbers and increased conservation efforts.

Measles virus is a single-stranded, negative-sense RNA virus belonging to the genus Morbillivirus in the family Paramyxoviridae. It is the causative agent of measles, a highly contagious infectious disease characterized by fever, cough, runny nose, and a red, blotchy rash. The virus primarily infects the respiratory tract and then spreads throughout the body via the bloodstream.

The genome of the measles virus is approximately 16 kilobases in length and encodes for eight proteins: nucleocapsid (N), phosphoprotein (P), matrix protein (M), fusion protein (F), hemagglutinin (H), large protein (L), and two non-structural proteins, V and C. The H protein is responsible for binding to the host cell receptor CD150 (SLAM) and mediating viral entry, while the F protein facilitates fusion of the viral and host cell membranes.

Measles virus is transmitted through respiratory droplets and direct contact with infected individuals. The virus can remain airborne for up to two hours in a closed space, making it highly contagious. Measles is preventable through vaccination, which has led to significant reductions in the incidence of the disease worldwide.

Viral proteins are the proteins that are encoded by the viral genome and are essential for the viral life cycle. These proteins can be structural or non-structural and play various roles in the virus's replication, infection, and assembly process. Structural proteins make up the physical structure of the virus, including the capsid (the protein shell that surrounds the viral genome) and any envelope proteins (that may be present on enveloped viruses). Non-structural proteins are involved in the replication of the viral genome and modulation of the host cell environment to favor viral replication. Overall, a thorough understanding of viral proteins is crucial for developing antiviral therapies and vaccines.

Vero cells are a line of cultured kidney epithelial cells that were isolated from an African green monkey (Cercopithecus aethiops) in the 1960s. They are named after the location where they were initially developed, the Vervet Research Institute in Japan.

Vero cells have the ability to divide indefinitely under certain laboratory conditions and are often used in scientific research, including virology, as a host cell for viruses to replicate. This allows researchers to study the characteristics of various viruses, such as their growth patterns and interactions with host cells. Vero cells are also used in the production of some vaccines, including those for rabies, polio, and Japanese encephalitis.

It is important to note that while Vero cells have been widely used in research and vaccine production, they can still have variations between different cell lines due to factors like passage number or culture conditions. Therefore, it's essential to specify the exact source and condition of Vero cells when reporting experimental results.

Newcastle Disease is a highly contagious viral disease caused by the Newcastle Disease Virus (NDV). It primarily affects birds and poultry, causing severe respiratory, neurological, and gastrointestinal symptoms. The virus can also infect mammals, including humans, but human cases are relatively rare and usually result in mild or asymptomatic infections.

In birds, the disease can cause significant mortality, especially in young chickens. Symptoms may include respiratory distress, depression, greenish diarrhea, muscle tremors, twisting of the neck (torticollis), paralysis, and decreased egg production. The virus is transmitted through direct contact with infected birds or their feces, as well as through contaminated food, water, and equipment.

In humans, Newcastle Disease typically results in conjunctivitis, mild respiratory symptoms, or influenza-like illness. It is not considered a significant public health concern, but proper biosecurity measures should be taken to prevent transmission between birds and humans. Vaccination programs are widely used to control the disease in poultry populations.

Nucleocapsid proteins are structural proteins that are associated with the viral genome in many viruses. They play a crucial role in the formation and stability of the viral particle, also known as the virion. In particular, nucleocapsid proteins bind to the viral RNA or DNA genome and help to protect it from degradation by host cell enzymes. They also participate in the assembly and disassembly of the virion during the viral replication cycle.

In some viruses, such as coronaviruses, the nucleocapsid protein is also involved in regulating the transcription and replication of the viral genome. The nucleocapsid protein of SARS-CoV-2, for example, has been shown to interact with host cell proteins that are involved in the regulation of gene expression, which may contribute to the virus's ability to manipulate the host cell environment and evade the immune response.

Overall, nucleocapsid proteins are important components of many viruses and are often targeted by antiviral therapies due to their essential role in the viral replication cycle.

A viral genome is the genetic material (DNA or RNA) that is present in a virus. It contains all the genetic information that a virus needs to replicate itself and infect its host. The size and complexity of viral genomes can vary greatly, ranging from a few thousand bases to hundreds of thousands of bases. Some viruses have linear genomes, while others have circular genomes. The genome of a virus also contains the information necessary for the virus to hijack the host cell's machinery and use it to produce new copies of the virus. Understanding the genetic makeup of viruses is important for developing vaccines and antiviral treatments.

Respiratory Syncytial Viruses (RSV) are a common type of virus that cause respiratory infections, particularly in young children and older adults. They are responsible for inflammation and narrowing of the small airways in the lungs, leading to breathing difficulties and other symptoms associated with bronchiolitis and pneumonia.

The term "syncytial" refers to the ability of these viruses to cause infected cells to merge and form large multinucleated cells called syncytia, which is a characteristic feature of RSV infections. The virus spreads through respiratory droplets when an infected person coughs or sneezes, and it can also survive on surfaces for several hours, making transmission easy.

RSV infections are most common during the winter months and can cause mild to severe symptoms depending on factors such as age, overall health, and underlying medical conditions. While RSV is typically associated with respiratory illnesses in children, it can also cause significant disease in older adults and immunocompromised individuals. Currently, there is no vaccine available for RSV, but antiviral medications and supportive care are used to manage severe infections.

'Cercopithecus aethiops' is the scientific name for the monkey species more commonly known as the green monkey. It belongs to the family Cercopithecidae and is native to western Africa. The green monkey is omnivorous, with a diet that includes fruits, nuts, seeds, insects, and small vertebrates. They are known for their distinctive greenish-brown fur and long tail. Green monkeys are also important animal models in biomedical research due to their susceptibility to certain diseases, such as SIV (simian immunodeficiency virus), which is closely related to HIV.

Respiratory Syncytial Virus (RSV) infections refer to the clinical illnesses caused by the Respiratory Syncytial Virus. RSV is a highly contagious virus that spreads through respiratory droplets, contact with infected surfaces, or direct contact with infected people. It primarily infects the respiratory tract, causing inflammation and damage to the cells lining the airways.

RSV infections can lead to a range of respiratory illnesses, from mild, cold-like symptoms to more severe conditions such as bronchiolitis (inflammation of the small airways in the lungs) and pneumonia (infection of the lung tissue). The severity of the infection tends to depend on factors like age, overall health status, and presence of underlying medical conditions.

In infants and young children, RSV is a leading cause of bronchiolitis and pneumonia, often resulting in hospitalization. In older adults, people with weakened immune systems, and those with chronic heart or lung conditions, RSV infections can also be severe and potentially life-threatening.

Symptoms of RSV infection may include runny nose, cough, sneezing, fever, wheezing, and difficulty breathing. Treatment typically focuses on managing symptoms and providing supportive care, although hospitalization and more aggressive interventions may be necessary in severe cases or for high-risk individuals. Preventive measures such as hand hygiene, wearing masks, and avoiding close contact with infected individuals can help reduce the spread of RSV.

Phylogeny is the evolutionary history and relationship among biological entities, such as species or genes, based on their shared characteristics. In other words, it refers to the branching pattern of evolution that shows how various organisms have descended from a common ancestor over time. Phylogenetic analysis involves constructing a tree-like diagram called a phylogenetic tree, which depicts the inferred evolutionary relationships among organisms or genes based on molecular sequence data or other types of characters. This information is crucial for understanding the diversity and distribution of life on Earth, as well as for studying the emergence and spread of diseases.

Molecular sequence data refers to the specific arrangement of molecules, most commonly nucleotides in DNA or RNA, or amino acids in proteins, that make up a biological macromolecule. This data is generated through laboratory techniques such as sequencing, and provides information about the exact order of the constituent molecules. This data is crucial in various fields of biology, including genetics, evolution, and molecular biology, allowing for comparisons between different organisms, identification of genetic variations, and studies of gene function and regulation.

A viral RNA (ribonucleic acid) is the genetic material found in certain types of viruses, as opposed to viruses that contain DNA (deoxyribonucleic acid). These viruses are known as RNA viruses. The RNA can be single-stranded or double-stranded and can exist as several different forms, such as positive-sense, negative-sense, or ambisense RNA. Upon infecting a host cell, the viral RNA uses the host's cellular machinery to translate the genetic information into proteins, leading to the production of new virus particles and the continuation of the viral life cycle. Examples of human diseases caused by RNA viruses include influenza, COVID-19 (SARS-CoV-2), hepatitis C, and polio.

A cell line is a culture of cells that are grown in a laboratory for use in research. These cells are usually taken from a single cell or group of cells, and they are able to divide and grow continuously in the lab. Cell lines can come from many different sources, including animals, plants, and humans. They are often used in scientific research to study cellular processes, disease mechanisms, and to test new drugs or treatments. Some common types of human cell lines include HeLa cells (which come from a cancer patient named Henrietta Lacks), HEK293 cells (which come from embryonic kidney cells), and HUVEC cells (which come from umbilical vein endothelial cells). It is important to note that cell lines are not the same as primary cells, which are cells that are taken directly from a living organism and have not been grown in the lab.

An amino acid sequence is the specific order of amino acids in a protein or peptide molecule, formed by the linking of the amino group (-NH2) of one amino acid to the carboxyl group (-COOH) of another amino acid through a peptide bond. The sequence is determined by the genetic code and is unique to each type of protein or peptide. It plays a crucial role in determining the three-dimensional structure and function of proteins.

Virus replication is the process by which a virus produces copies or reproduces itself inside a host cell. This involves several steps:

1. Attachment: The virus attaches to a specific receptor on the surface of the host cell.
2. Penetration: The viral genetic material enters the host cell, either by invagination of the cell membrane or endocytosis.
3. Uncoating: The viral genetic material is released from its protective coat (capsid) inside the host cell.
4. Replication: The viral genetic material uses the host cell's machinery to produce new viral components, such as proteins and nucleic acids.
5. Assembly: The newly synthesized viral components are assembled into new virus particles.
6. Release: The newly formed viruses are released from the host cell, often through lysis (breaking) of the cell membrane or by budding off the cell membrane.

The specific mechanisms and details of virus replication can vary depending on the type of virus. Some viruses, such as DNA viruses, use the host cell's DNA polymerase to replicate their genetic material, while others, such as RNA viruses, use their own RNA-dependent RNA polymerase or reverse transcriptase enzymes. Understanding the process of virus replication is important for developing antiviral therapies and vaccines.

Antibodies, viral are proteins produced by the immune system in response to an infection with a virus. These antibodies are capable of recognizing and binding to specific antigens on the surface of the virus, which helps to neutralize or destroy the virus and prevent its replication. Once produced, these antibodies can provide immunity against future infections with the same virus.

Viral antibodies are typically composed of four polypeptide chains - two heavy chains and two light chains - that are held together by disulfide bonds. The binding site for the antigen is located at the tip of the Y-shaped structure, formed by the variable regions of the heavy and light chains.

There are five classes of antibodies in humans: IgA, IgD, IgE, IgG, and IgM. Each class has a different function and is distributed differently throughout the body. For example, IgG is the most common type of antibody found in the bloodstream and provides long-term immunity against viruses, while IgA is found primarily in mucous membranes and helps to protect against respiratory and gastrointestinal infections.

In addition to their role in the immune response, viral antibodies can also be used as diagnostic tools to detect the presence of a specific virus in a patient's blood or other bodily fluids.

A base sequence in the context of molecular biology refers to the specific order of nucleotides in a DNA or RNA molecule. In DNA, these nucleotides are adenine (A), guanine (G), cytosine (C), and thymine (T). In RNA, uracil (U) takes the place of thymine. The base sequence contains genetic information that is transcribed into RNA and ultimately translated into proteins. It is the exact order of these bases that determines the genetic code and thus the function of the DNA or RNA molecule.

Viral pneumonia is a type of pneumonia caused by viral infection. It primarily affects the upper and lower respiratory tract, leading to inflammation of the alveoli (air sacs) in the lungs. This results in symptoms such as cough, difficulty breathing, fever, fatigue, and chest pain. Common viruses that can cause pneumonia include influenza virus, respiratory syncytial virus (RSV), and adenovirus. Viral pneumonia is often milder than bacterial pneumonia but can still be serious, especially in young children, older adults, and people with weakened immune systems. Treatment typically involves supportive care, such as rest, hydration, and fever reduction, while the body fights off the virus. In some cases, antiviral medications may be used to help manage symptoms and prevent complications.

Pneumonia is an infection or inflammation of the alveoli (tiny air sacs) in one or both lungs. It's often caused by bacteria, viruses, or fungi. Accumulated pus and fluid in these air sacs make it difficult to breathe, which can lead to coughing, chest pain, fever, and difficulty breathing. The severity of symptoms can vary from mild to life-threatening, depending on the underlying cause, the patient's overall health, and age. Pneumonia is typically diagnosed through a combination of physical examination, medical history, and diagnostic tests such as chest X-rays or blood tests. Treatment usually involves antibiotics for bacterial pneumonia, antivirals for viral pneumonia, and supportive care like oxygen therapy, hydration, and rest.

Bacterial pneumonia is a type of lung infection that's caused by bacteria. It can affect people of any age, but it's more common in older adults, young children, and people with certain health conditions or weakened immune systems. The symptoms of bacterial pneumonia can vary, but they often include cough, chest pain, fever, chills, and difficulty breathing.

The most common type of bacteria that causes pneumonia is Streptococcus pneumoniae (pneumococcus). Other types of bacteria that can cause pneumonia include Haemophilus influenzae, Staphylococcus aureus, and Mycoplasma pneumoniae.

Bacterial pneumonia is usually treated with antibiotics, which are medications that kill bacteria. The specific type of antibiotic used will depend on the type of bacteria causing the infection. It's important to take all of the prescribed medication as directed, even if you start feeling better, to ensure that the infection is completely cleared and to prevent the development of antibiotic resistance.

In severe cases of bacterial pneumonia, hospitalization may be necessary for close monitoring and treatment with intravenous antibiotics and other supportive care.

Parainfluenza Virus 1, Human (HPIV-1) is a type of respiratory virus that belongs to the family Paramyxoviridae and genus Respirovirus. It is one of the four serotypes of human parainfluenza viruses (HPIVs), which are important causes of acute respiratory infections in children, immunocompromised individuals, and the elderly.

HPIV-1 primarily infects the upper respiratory tract, causing symptoms such as cough, runny nose, sore throat, and fever. However, it can also cause lower respiratory tract infections, including bronchitis, bronchiolitis, and pneumonia, particularly in young children and infants.

HPIV-1 is transmitted through respiratory droplets or direct contact with infected individuals. The incubation period for HPIV-1 infection ranges from 2 to 7 days, after which symptoms can last for up to 10 days. There is no specific antiviral treatment available for HPIV-1 infections, and management typically involves supportive care such as hydration, fever reduction, and respiratory support if necessary.

Prevention measures include good hand hygiene, avoiding close contact with infected individuals, and practicing cough etiquette. Vaccines are not currently available for HPIV-1 infections, but research is ongoing to develop effective vaccines against these viruses.

Influenza, also known as the flu, is a highly contagious viral infection that attacks the respiratory system of humans. It is caused by influenza viruses A, B, or C and is characterized by the sudden onset of fever, chills, headache, muscle pain, sore throat, cough, runny nose, and fatigue. Influenza can lead to complications such as pneumonia, bronchitis, and ear infections, and can be particularly dangerous for young children, older adults, pregnant women, and people with weakened immune systems or chronic medical conditions. The virus is spread through respiratory droplets produced when an infected person coughs, sneezes, or talks, and can also survive on surfaces for a period of time. Influenza viruses are constantly changing, which makes it necessary to get vaccinated annually to protect against the most recent and prevalent strains.

'Influenza A Virus, H1N1 Subtype' is a specific subtype of the influenza A virus that causes flu in humans and animals. It contains certain proteins called hemagglutinin (H) and neuraminidase (N) on its surface, with this subtype specifically having H1 and N1 antigens. The H1N1 strain is well-known for causing the 2009 swine flu pandemic, which was a global outbreak of flu that resulted in significant morbidity and mortality. This subtype can also cause seasonal flu, although the severity and symptoms may vary. It is important to note that influenza viruses are constantly changing, and new strains or subtypes can emerge over time, requiring regular updates to vaccines to protect against them.

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