Infections with viruses of the genus FLAVIVIRUS, family FLAVIVIRIDAE.
A genus of FLAVIVIRIDAE containing several subgroups and many species. Most are arboviruses transmitted by mosquitoes or ticks. The type species is YELLOW FEVER VIRUS.
A species of FLAVIVIRUS, one of the Japanese encephalitis virus group (ENCEPHALITIS VIRUSES, JAPANESE). It can infect birds and mammals. In humans, it is seen most frequently in Africa, Asia, and Europe presenting as a silent infection or undifferentiated fever (WEST NILE FEVER). The virus appeared in North America for the first time in 1999. It is transmitted mainly by CULEX spp mosquitoes which feed primarily on birds, but it can also be carried by the Asian Tiger mosquito, AEDES albopictus, which feeds mainly on mammals.
Encephalitis caused by neurotropic viruses that are transmitted via the bite of TICKS. In Europe, the diseases are caused by ENCEPHALITIS VIRUSES, TICK-BORNE, which give rise to Russian spring-summer encephalitis, central European encephalitis, louping ill encephalitis, and related disorders. Powassan encephalitis occurs in North America and Russia and is caused by the Powassan virus. ASEPTIC MENINGITIS and rarely encephalitis may complicate COLORADO TICK FEVER which is endemic to mountainous regions of the western United States. (From Joynt, Clinical Neurology, 1996, Ch26, pp14-5)
Virus diseases caused by the TOGAVIRIDAE.
A subgroup of the genus FLAVIVIRUS that causes encephalitis and hemorrhagic fevers and is found in eastern and western Europe and the former Soviet Union. It is transmitted by TICKS and there is an associated milk-borne transmission from viremic cattle, goats, and sheep.
A species of FLAVIVIRUS, one of the Japanese encephalitis virus group (ENCEPHALITIS VIRUSES, JAPANESE), which is the etiological agent of Japanese encephalitis found in Asia, southeast Asia, and the Indian subcontinent.
Infections of the brain caused by arthropod-borne viruses (i.e., arboviruses) primarily from the families TOGAVIRIDAE; FLAVIVIRIDAE; BUNYAVIRIDAE; REOVIRIDAE; and RHABDOVIRIDAE. Life cycles of these viruses are characterized by ZOONOSES, with birds and lower mammals serving as intermediate hosts. The virus is transmitted to humans by the bite of mosquitoes (CULICIDAE) or TICKS. Clinical manifestations include fever, headache, alterations of mentation, focal neurologic deficits, and COMA. (From Clin Microbiol Rev 1994 Jan;7(1):89-116; Walton, Brain's Diseases of the Nervous System, 10th ed, p321)
A mosquito-borne encephalitis caused by the Japanese B encephalitis virus (ENCEPHALITIS VIRUS, JAPANESE) occurring throughout Eastern Asia and Australia. The majority of infections occur in children and are subclinical or have features limited to transient fever and gastrointestinal symptoms. Inflammation of the brain, spinal cord, and meninges may occur and lead to transient or permanent neurologic deficits (including a POLIOMYELITIS-like presentation); SEIZURES; COMA; and death. (From Adams et al., Principles of Neurology, 6th ed, p751; Lancet 1998 Apr 11;351(9109):1094-7)
A species of FLAVIVIRUS, one of the Japanese encephalitis virus group (ENCEPHALITIS VIRUSES, JAPANESE), found in Australia and New Guinea. It causes a fulminating viremia resembling Japanese encephalitis (ENCEPHALITIS, JAPANESE).
A species of the genus FLAVIVIRUS which causes an acute febrile and sometimes hemorrhagic disease in man. Dengue is mosquito-borne and four serotypes are known.
A mosquito-borne viral illness caused by the WEST NILE VIRUS, a FLAVIVIRUS and endemic to regions of Africa, Asia, and Europe. Common clinical features include HEADACHE; FEVER; maculopapular rash; gastrointestinal symptoms; and lymphadenopathy. MENINGITIS; ENCEPHALITIS; and MYELITIS may also occur. The disease may occasionally be fatal or leave survivors with residual neurologic deficits. (From Joynt, Clinical Neurology, 1996, Ch26, p13; Lancet 1998 Sep 5;352(9130):767-71)
An acute febrile disease transmitted by the bite of AEDES mosquitoes infected with DENGUE VIRUS. It is self-limiting and characterized by fever, myalgia, headache, and rash. SEVERE DENGUE is a more virulent form of dengue.
Immunoglobulins produced in response to VIRAL ANTIGENS.
A subgroup of the genus FLAVIVIRUS which comprises a number of viral species that are the etiologic agents of human encephalitis in many different geographical regions. These include Japanese encephalitis virus (ENCEPHALITIS VIRUS, JAPANESE), St. Louis encephalitis virus (ENCEPHALITIS VIRUS, ST. LOUIS), Murray Valley encephalitis virus (ENCEPHALITIS VIRUS, MURRAY VALLEY), and WEST NILE 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.
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.
Layers of protein which surround the capsid in animal viruses with tubular nucleocapsids. The envelope consists of an inner layer of lipids and virus specified proteins also called membrane or matrix proteins. The outer layer consists of one or more types of morphological subunits called peplomers which project from the viral envelope; this layer always consists of glycoproteins.
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.
Serological reactions in which an antiserum against one antigen reacts with a non-identical but closely related antigen.
A subfamily in the family MURIDAE, comprising the hamsters. Four of the more common genera are Cricetus, CRICETULUS; MESOCRICETUS; and PHODOPUS.
The type species of the FLAVIVIRUS genus. Principal vector transmission to humans is by AEDES spp. mosquitoes.
A class of immunoglobulin bearing mu chains (IMMUNOGLOBULIN MU-CHAINS). IgM can fix COMPLEMENT. The name comes from its high molecular weight and originally being called a macroglobulin.
Established cell cultures that have the potential to propagate indefinitely.
Proteins encoded by a VIRAL GENOME that are produced in the organisms they infect, but not packaged into the VIRUS PARTICLES. Some of these proteins may play roles within the infected cell during VIRUS REPLICATION or act in regulation of virus replication or VIRUS ASSEMBLY.
A species of FLAVIVIRUS, one of the Japanese encephalitis virus group (ENCEPHALITIS VIRUSES, JAPANESE), which is the etiologic agent of ST. LOUIS ENCEPHALITIS in the United States, the Caribbean, and Central and South America.
A family of the order DIPTERA that comprises the mosquitoes. The larval stages are aquatic, and the adults can be recognized by the characteristic WINGS, ANIMAL venation, the scales along the wing veins, and the long proboscis. Many species are of particular medical importance.
A genus of mosquitoes (CULICIDAE) commonly found in tropical regions. Species of this genus are vectors for ST. LOUIS ENCEPHALITIS as well as many other diseases of man and domestic and wild animals.
Ribonucleic acid that makes up the genetic material of viruses.
Vaccines or candidate vaccines used to prevent infection with WEST NILE VIRUS.
A viral encephalitis caused by the St. Louis encephalitis virus (ENCEPHALITIS VIRUS, ST. LOUIS), a FLAVIVIRUS. It is transmitted to humans and other vertebrates primarily by mosquitoes of the genus CULEX. The primary animal vectors are wild birds and the disorder is endemic to the midwestern and southeastern United States. Infections may be limited to an influenza-like illness or present as an ASEPTIC MENINGITIS or ENCEPHALITIS. Clinical manifestations of the encephalitic presentation may include SEIZURES, lethargy, MYOCLONUS, focal neurologic signs, COMA, and DEATH. (From Adams et al., Principles of Neurology, 6th ed, p750)
Works containing information articles on subjects in every field of knowledge, usually arranged in alphabetical order, or a similar work limited to a special field or subject. (From The ALA Glossary of Library and Information Science, 1983)
Viruses whose hosts are bacterial cells.
Viruses whose genetic material is RNA.
The type species of ORTHOPOXVIRUS, related to COWPOX VIRUS, but whose true origin is unknown. It has been used as a live vaccine against SMALLPOX. It is also used as a vector for inserting foreign DNA into animals. Rabbitpox virus is a subspecies of VACCINIA VIRUS.
Specific molecular components of the cell capable of recognizing and interacting with a virus, and which, after binding it, are capable of generating some signal that initiates the chain of events leading to the biological response.
Process of growing viruses in live animals, plants, or cultured cells.

Development and characterization of new flavivirus-resistant mouse strains bearing Flv(r)-like and Flv(mr) alleles from wild or wild-derived mice. (1/158)

A single genetic locus, flavivirus resistance (Flv), controls virus titres and severity of flavivirus infection in mouse brain. It has been mapped to mouse chromosome 5 and shown to include different allelic forms. While the majority of laboratory mouse strains are susceptible to flaviviruses and carry the Flv(s) allele, wild mice and laboratory mouse strains recently derived from them are resistant and carry flavivirus-resistance alleles including Flv(r)-like and Flv(mr) alleles. Although there is a mouse model of flavivirus resistance conferred by the Flv(r) allele, other resistance alleles have not been adequately studied due to a lack of appropriate animal models. In this paper we describe the development of new flavivirus-resistant mouse strains, C3H.M.domesticus-Flv(r) and C3H.MOLD-Flv(mr), which carry the novel resistance alleles Flv(r)-like and Flv(mr) on the genetic background of flavivirus susceptible C3H/HeJ mice. The new strains were created by 10 to 11 generations of backcrossing followed by brother-sister matings resulting in a generation of homozygous founder stocks. Genome analysis of the newly developed mouse strains has revealed chromosomal regions of approximately 9 and 11 cM, respectively, encompassing Flv on chromosome 5, which are derived from resistant donor mice. These segments are much smaller than the segment of approximately 31 cM described in the congenic resistant mouse strain C3H.PRI-Flv(r) (also known as C3H/RV). The new congenic mouse strains, which were created to carry the Flv(r)-like and Flv(mr) alleles on the standardized genetic background of susceptible mice, represent new animal models of flavivirus resistance conferred by these novel resistance alleles.  (+info)

Phylogeny of the genus flavivirus using complete coding sequences of arthropod-borne viruses and viruses with no known vector. (2/158)

Attempts to define the evolutionary relationships and origins of viruses in the genus Flavivirus are hampered by the lack of genetic information particularly amongst the non-vectored flaviviruses. Using a novel protocol for sequence determination, the first complete coding sequence of St Louis encephalitis virus and those of two representative non-vectored flaviviruses, Rio Bravo (isolated from bat) and Apoi (isolated from rodent), are reported. The encoded polyproteins of Rio Bravo and Apoi virus are the smallest described to date within the genus FLAVIVIRUS: The highest similarities with other flaviviruses were found in the NS3 and NS5 genes. The proteolytic cleavage sites for the viral serine protease were highly conserved among the flaviviruses completely sequenced to date. Comparative genetic amino acid alignments revealed that p-distance cut-off values of 0.330-0.470 distinguished the arthropod-borne viruses according to their recognized serogroups and Rio Bravo and Apoi virus were assigned to two distinct non-vectored virus groups. Within these serogroups, cladogenesis based on the complete ORF sequence was similar to trees based on envelope and NS5 sequences. In contrast, branching patterns at the deeper nodes of the tree were different from those reported in the previous study of NS5 sequences. The significance of these observations is discussed.  (+info)

Detection of anti-arboviral immunoglobulin G by using a monoclonal antibody-based capture enzyme-linked immunosorbent assay. (3/158)

Monoclonal antibody (MAb)-based capture enzyme-linked immunosorbent assays (ELISAs) for the detection of anti-arboviral immunoglobulin G (IgG ELISAs) were developed for a comprehensive array of medically important arboviruses from the Alphavirus, Flavivirus, and Bunyavirus genera. Tests were optimized and standardized so that maximum homology could be maintained among working parameters for the different viral agents, enabling a wide range of viruses to be easily tested for at one time. MAbs were screened for suitability as capture vehicles for antigens from the three genera. The final test configuration utilized group-reactive MAbs eastern equine encephalitis virus 1A4B-6, dengue 2 virus 4G2, and La Crosse encephalitis virus 10G5.4 to capture the specific inactivated viral antigens. Serum IgG was detected by using alkaline phosphatase-conjugated anti-human IgG (Fc portion). A dilution of 1:400 was chosen as the universal screening serum dilution, with endpoint titrations of serum samples testing positive eliminating occasional false-positive results. IgG ELISA results correlated with those of the standard plaque-reduction neutralization assays. As expected, some test cross-reactivity was encountered within the individual genera, and tests were interpreted within the context of these reactions. The tests were standardized for laboratory diagnosis of arboviral infections, with the intent that they be used in tandem with the corresponding IgM antibody-capture ELISAs.  (+info)

A novel model for the study of the therapy of flavivirus infections using the Modoc virus. (4/158)

The murine Flavivirus Modoc replicates well in Vero cells and appears to be as equally sensitive as both yellow fever and dengue fever virus to a selection of antiviral agents. Infection of SCID mice, by either the intracerebral, intraperitoneal, or intranasal route, results in 100% mortality. Immunocompetent mice and hamsters proved to be susceptible to the virus only when inoculated via the intranasal or intracerebral route. Animals ultimately die of (histologically proven) encephalitis with features similar to Flavivirus encephalitis in man. Viral RNA was detected in the brain, spleen, and salivary glands of infected SCID mice and the brain, lung, kidney, and salivary glands of infected hamsters. In SCID mice, the interferon inducer poly IC protected against Modoc virus-induced morbidity and mortality and this protection was associated with a reduction in infectious virus content and viral RNA load. Infected hamsters shed the virus in the urine. This allows daily monitoring of (inhibition of) viral replication, by means of a noninvasive method and in the same animal. The Modoc virus model appears attractive for the study of chemoprophylactic or chemotherapeutic strategies against Flavivirus infections.  (+info)

Innate resistance to flavivirus infection in mice controlled by Flv is nitric oxide-independent. (5/158)

Innate resistance to flaviviruses in mice is active in the brain where it restricts virus replication. This resistance is controlled by a single genetic locus, FLV, located on mouse chromosome 5 near the locus encoding the neuronal form of nitric oxide synthase (Nos1). Since nitric oxide (NO) has been implicated in antiviral activity, its involvement in natural resistance to flaviviruses has been hypothesized. Here we present data on NO production before and during flavivirus infection in both brain tissue and peritoneal macrophages from two flavivirus-resistant (FLV(r)) and one congenic susceptible (FLV(s)) mouse strains. This study provides evidence that NO is not involved in the expression of flavivirus resistance controlled by FLV since: (a) there is no difference in brain tissue NO levels between susceptible and resistant mice, and (b) lipopolysaccharide-induced NO does not abrogate the difference in flavivirus replication in peritoneal macrophages from susceptible and resistant mice.  (+info)

Comparison of flavivirus universal primer pairs and development of a rapid, highly sensitive heminested reverse transcription-PCR assay for detection of flaviviruses targeted to a conserved region of the NS5 gene sequences. (6/158)

Arthropod-transmitted flaviviruses are responsible for considerable morbidity and mortality, causing severe encephalitic, hemorrhagic, and febrile illnesses in humans. Because there are no specific clinical symptoms for infection by a determined virus and because different arboviruses could be present in the same area, a genus diagnosis by PCR would be a useful first-line diagnostic method. The six published Flavivirus genus primer pairs localized in the NS1, NS3, NS5, and 3' NC regions were evaluated in terms of specificity and sensitivity with flaviviruses (including the main viruses pathogenic for humans) at a titer of 10(5) 50% tissue culture infectious doses (TCID(50)s) ml(-1) with a common identification step by agarose gel electrophoresis. Only one NS5 primer pair allowed the detection of all tested flaviviruses with the sensitivity limit of 10(5) TCID(50)s ml(-1). Using a heminested PCR with new primers designed in the same region after an alignment of 30 different flaviviruses, the sensitivity of reverse transcription-PCR was improved and allowed the detection of about 200 infectious doses ml(-1) with all of the tick- and mosquito-borne flaviviruses tested. It was confirmed that the sequenced amplified products in the NS5 region allowed predictability of flavivirus species by dendrogram, including the New York 99 West Nile strain. This technique was successfully performed with a cerebrospinal fluid sample from a patient hospitalized with West Nile virus encephalitis.  (+info)

Modulation of transporter associated with antigen processing (TAP)-mediated peptide import into the endoplasmic reticulum by flavivirus infection. (7/158)

In contrast to many other viruses that escape the cellular immune response by downregulating major histocompatibility complex (MHC) class I molecules, flavivirus infection can upregulate their cell surface expression. Previously we have presented evidence that during flavivirus infection, peptide supply to the endoplasmic reticulum is increased (A. Mullbacher and M. Lobigs, Immunity 3:207-214, 1995). Here we show that during the early phase of infection with different flaviviruses, the transport activity of the peptide transporter associated with antigen processing (TAP) is augmented by up to 50%. TAP expression is unaltered during infection, and viral but not host macromolecular synthesis is required for enhanced peptide transport. This study is the first demonstration of transient enhancement of TAP-dependent peptide import into the lumen of the endoplasmic reticulum as a consequence of a viral infection. We suggest that the increased supply of peptides for assembly with MHC class I molecules in flavivirus-infected cells accounts for the upregulation of MHC class I cell surface expression with the biological consequence of viral evasion of natural killer cell recognition.  (+info)

Encephalitis and retarded growth of chicks caused by Sitiawan virus, a new isolate belonging to the genus Flavivirus. (8/158)

A new virus named Sitiawan virus (SV) was isolated from sick broiler chicks in chicken embryos. The virus replicated well with cytopathogenic effect (CPE) in the chicken B-lymphocyte cell line LSCC-BK3. The virus was an enveloped RNA virus of approximately 41 nm in size with hemagglutinating activity (HA) to goose erythrocytes. It was cross-reactive with Japanese encephalitis virus (JEV), a member of flaviviruses by HA inhibition tests but not by cross-virus neutralization tests. The cDNA fragment of NS5 gene was amplified with primers corresponding to NS5 gene of flaviviruses. The nucleotide sequences were 92% homologous to Tembusu virus, a member of the mosquito-borne virus cluster of the genus Flavivirus. In cross-neutralization tests with Tembusu virus, antiserum to SV did not neutralize Tembusu virus, and antiserum to Tembusu virus neutralized more weakly to SV than against homologous virus. These results indicate that SV is a new virus which can be differentiated serologically from Tembusu virus but is otherwise similar with respect to nucleotide sequence. The virus causes encephalitis, growth retardation, and increased blood glucose levels in inoculated chicks.  (+info)

Flavivirus infections refer to a group of diseases caused by various viruses belonging to the Flaviviridae family, specifically within the genus Flavivirus. These viruses are primarily transmitted to humans through the bites of infected arthropods, such as mosquitoes and ticks.

Some well-known flavivirus infections include:

1. Dengue Fever: A mosquito-borne viral infection that is prevalent in tropical and subtropical regions worldwide. It can cause a wide range of symptoms, from mild flu-like illness to severe complications like dengue hemorrhagic fever and dengue shock syndrome.
2. Yellow Fever: A viral hemorrhagic disease transmitted by the Aedes and Haemagogus mosquitoes, primarily in Africa and South America. It can cause severe illness, including jaundice, bleeding, organ failure, and death.
3. Japanese Encephalitis: A mosquito-borne viral infection that is endemic to Southeast Asia and the Western Pacific. While most infections are asymptomatic or mild, a small percentage of cases can lead to severe neurological complications, such as encephalitis (inflammation of the brain) and meningitis (inflammation of the membranes surrounding the brain and spinal cord).
4. Zika Virus Infection: A mosquito-borne viral disease that has spread to many regions of the world, particularly in tropical and subtropical areas. Most Zika virus infections are mild or asymptomatic; however, infection during pregnancy can cause severe birth defects, such as microcephaly (abnormally small head size) and other neurological abnormalities in the developing fetus.
5. West Nile Virus Infection: A mosquito-borne viral disease that is endemic to North America, Europe, Africa, Asia, and Australia. Most infections are mild or asymptomatic; however, a small percentage of cases can lead to severe neurological complications, such as encephalitis, meningitis, and acute flaccid paralysis (sudden weakness in the arms and legs).

Prevention measures for these diseases typically involve avoiding mosquito bites through the use of insect repellent, wearing long sleeves and pants, staying indoors during peak mosquito hours, and removing standing water from around homes and businesses. Additionally, vaccines are available for some of these diseases, such as Japanese encephalitis and yellow fever, and should be considered for individuals traveling to areas where these diseases are common.

Flavivirus is a genus of viruses in the family Flaviviridae. They are enveloped, single-stranded, positive-sense RNA viruses that are primarily transmitted by arthropod vectors such as mosquitoes and ticks. Many flaviviruses cause significant disease in humans, including dengue fever, yellow fever, Japanese encephalitis, West Nile fever, and Zika fever. The name "flavivirus" is derived from the Latin word for "yellow," referring to the yellow fever virus, which was one of the first members of this genus to be discovered.

West Nile Virus (WNV) is an Flavivirus, which is a type of virus that is spread by mosquitoes. It was first discovered in the West Nile district of Uganda in 1937 and has since been found in many countries throughout the world. WNV can cause a mild to severe illness known as West Nile fever.

Most people who become infected with WNV do not develop any symptoms, but some may experience fever, headache, body aches, joint pain, vomiting, diarrhea, or a rash. In rare cases, the virus can cause serious neurological illnesses such as encephalitis (inflammation of the brain) or meningitis (inflammation of the membranes surrounding the brain and spinal cord). These severe forms of the disease can be fatal, especially in older adults and people with weakened immune systems.

WNV is primarily transmitted to humans through the bite of infected mosquitoes, but it can also be spread through blood transfusions, organ transplants, or from mother to baby during pregnancy, delivery, or breastfeeding. There is no specific treatment for WNV, and most people recover on their own with rest and supportive care. However, hospitalization may be necessary in severe cases. Prevention measures include avoiding mosquito bites by using insect repellent, wearing long sleeves and pants, and staying indoors during peak mosquito activity hours.

Tick-borne encephalitis (TBE) is a viral infectious disease that causes inflammation of the brain (encephalitis). It is transmitted to humans through the bite of infected ticks, primarily of the Ixodes species. The TBE virus belongs to the family Flaviviridae and has several subtypes, with different geographical distributions.

The illness typically progresses in two stages:

1. An initial viremic phase, characterized by fever, headache, fatigue, muscle pain, and sometimes rash, which lasts about a week.
2. A second neurological phase, which occurs in approximately 20-30% of infected individuals, can manifest as meningitis (inflammation of the membranes surrounding the brain and spinal cord), encephalitis (inflammation of the brain), or meningoencephalitis (inflammation of both the brain and its membranes). Symptoms may include neck stiffness, severe headache, confusion, disorientation, seizures, and in severe cases, coma and long-term neurological complications.

Preventive measures include avoiding tick-infested areas, using insect repellents, wearing protective clothing, and promptly removing attached ticks. Vaccination is available and recommended for individuals living or traveling to TBE endemic regions. Treatment is primarily supportive, focusing on managing symptoms and addressing complications as they arise. There is no specific antiviral treatment for TBE.

Togaviridae is a family of single-stranded, enveloped RNA viruses that includes several important pathogens affecting humans and animals. The most well-known member of this family is the genus Alphavirus, which includes viruses such as Chikungunya, Eastern equine encephalitis, Sindbis, O'nyong-nyong, Ross River, and Western equine encephalitis viruses.

Togaviridae infections typically cause symptoms such as fever, rash, arthralgia (joint pain), myalgia (muscle pain), and sometimes more severe manifestations like meningitis or encephalitis, depending on the specific virus and the host's immune status. The transmission of these viruses usually occurs through the bite of infected mosquitoes, although some members of this family can also be transmitted via other arthropod vectors or through contact with infected animals or their bodily fluids.

Prevention strategies for Togaviridae infections include using insect repellent, wearing protective clothing, and eliminating breeding sites for mosquitoes. Vaccines are available for some members of this family, such as the Eastern and Western equine encephalitis viruses, but not for others like Chikungunya virus. Treatment is generally supportive, focusing on relieving symptoms and managing complications.

Tick-borne encephalitis (TBE) viruses are a group of related viruses that are primarily transmitted to humans through the bite of infected ticks. The main strains of TBE viruses include:

1. European tick-borne encephalitis virus (TBEV-Eu): This strain is found mainly in Europe and causes the majority of human cases of TBE. It is transmitted by the tick species Ixodes ricinus.
2. Siberian tick-borne encephalitis virus (TBEV-Sib): This strain is prevalent in Russia, Mongolia, and China, and is transmitted by the tick species Ixodes persulcatus.
3. Far Eastern tick-borne encephalitis virus (TBEV-FE): Also known as Russian spring-summer encephalitis (RSSE) virus, this strain is found in Russia, China, and Japan, and is transmitted by the tick species Ixodes persulcatus.
4. Louping ill virus (LIV): This strain is primarily found in the United Kingdom, Ireland, Portugal, and Spain, and is transmitted by the tick species Ixodes ricinus. It mainly affects sheep but can also infect humans.
5. Turkish sheep encephalitis virus (TSEV): This strain is found in Turkey and Greece and is primarily associated with ovine encephalitis, although it can occasionally cause human disease.
6. Negishi virus (NGS): This strain has been identified in Japan and Russia, but its role in human disease remains unclear.

TBE viruses are members of the Flaviviridae family and are closely related to other mosquito-borne flaviviruses such as West Nile virus, dengue virus, and Zika virus. The incubation period for TBE is usually 7-14 days after a tick bite, but it can range from 2 to 28 days. Symptoms of TBE include fever, headache, muscle pain, fatigue, and vomiting, followed by neurological symptoms such as meningitis (inflammation of the membranes surrounding the brain and spinal cord) or encephalitis (inflammation of the brain). Severe cases can lead to long-term complications or even death. No specific antiviral treatment is available for TBE, and management typically involves supportive care. Prevention measures include avoiding tick-infested areas, using insect repellents, wearing protective clothing, and promptly removing attached ticks. Vaccination is also recommended for individuals at high risk of exposure to TBE viruses.

Japanese Encephalitis Virus (JEV) is a type of flavivirus that is the causative agent of Japanese encephalitis, a mosquito-borne viral infection of the brain. The virus is primarily transmitted to humans through the bite of infected Culex species mosquitoes, particularly Culex tritaeniorhynchus and Culex gelidus.

JEV is endemic in many parts of Asia, including China, Japan, Korea, India, Nepal, Thailand, and Vietnam. It is estimated to cause around 68,000 clinical cases and 13,000-20,000 deaths each year. The virus is maintained in a transmission cycle between mosquitoes and vertebrate hosts, primarily pigs and wading birds.

Most JEV infections are asymptomatic or result in mild symptoms such as fever, headache, and muscle aches. However, in some cases, the infection can progress to severe encephalitis, which is characterized by inflammation of the brain, leading to neurological symptoms such as seizures, tremors, paralysis, and coma. The case fatality rate for Japanese encephalitis is estimated to be 20-30%, and around half of those who survive have significant long-term neurological sequelae.

Prevention of JEV infection includes the use of insect repellent, wearing protective clothing, and avoiding outdoor activities during peak mosquito feeding times. Vaccination is also an effective means of preventing Japanese encephalitis, and vaccines are available for travelers to endemic areas as well as for residents of those areas.

Arbovirus encephalitis is a type of encephalitis (inflammation of the brain) caused by a group of viruses that are transmitted through the bite of infected arthropods, such as mosquitoes or ticks. The term "arbovirus" stands for "arthropod-borne virus."

There are many different types of arboviruses that can cause encephalitis, including:

* La Crosse virus
* St. Louis encephalitis virus
* West Nile virus
* Eastern equine encephalitis virus
* Western equine encephalitis virus
* Venezuelan equine encephalitis virus

The symptoms of arbovirus encephalitis can vary, but may include fever, headache, stiff neck, seizures, confusion, and weakness. In severe cases, it can lead to coma or death. Treatment typically involves supportive care to manage symptoms, as there is no specific antiviral treatment for most types of arbovirus encephalitis. Prevention measures include avoiding mosquito and tick bites, using insect repellent, and eliminating standing water where mosquitoes breed.

Japanese encephalitis is a viral inflammation of the brain (encephalitis) caused by the Japanese encephalitis virus (JEV). It is transmitted to humans through the bite of infected Culex mosquitoes, particularly in rural and agricultural areas. The majority of JE cases occur in children under the age of 15. Most people infected with JEV do not develop symptoms, but some may experience mild symptoms such as fever, headache, and vomiting. In severe cases, JEV can cause high fever, neck stiffness, seizures, confusion, and coma. There is no specific treatment for Japanese encephalitis, and care is focused on managing symptoms and supporting the patient's overall health. Prevention measures include vaccination and avoiding mosquito bites in endemic areas.

Murray Valley Encephalitis Virus (MVEV) is a type of arbovirus (arthropod-borne virus) that is primarily transmitted to humans through the bite of an infected mosquito. The virus is named after the Murray Valley region in Australia where it was first identified.

MVEV is the causative agent of Murray Valley encephalitis, a serious illness that can affect the brain and cause inflammation (encephalitis). The virus is found primarily in Australia, Papua New Guinea, and parts of Southeast Asia.

The transmission cycle of MVEV involves mosquitoes serving as vectors that transmit the virus between birds and mammals, including humans. Infection with MVEV can cause a range of symptoms, from mild fever and headache to severe neurological complications such as seizures, coma, and permanent brain damage. There is no specific treatment for Murray Valley encephalitis, and prevention efforts focus on reducing mosquito populations and avoiding mosquito bites in areas where the virus is known to be present.

Dengue virus (DENV) is a single-stranded, positive-sense RNA virus that belongs to the genus Flavivirus in the family Flaviviridae. It is primarily transmitted to humans through the bites of infected female mosquitoes, mainly Aedes aegypti and Aedes albopictus.

The DENV genome contains approximately 11,000 nucleotides and encodes three structural proteins (capsid, pre-membrane/membrane, and envelope) and seven non-structural proteins (NS1, NS2A, NS2B, NS3, NS4A, NS4B, and NS5). There are four distinct serotypes of DENV (DENV-1, DENV-2, DENV-3, and DENV-4), each of which can cause dengue fever, a mosquito-borne viral disease.

Infection with one serotype provides lifelong immunity against that particular serotype but only temporary and partial protection against the other three serotypes. Subsequent infections with different serotypes can increase the risk of developing severe dengue, such as dengue hemorrhagic fever or dengue shock syndrome, due to antibody-dependent enhancement (ADE) and original antigenic sin phenomena.

DENV is a significant public health concern in tropical and subtropical regions worldwide, with an estimated 390 million annual infections and approximately 100-400 million clinical cases. Preventive measures include vector control strategies to reduce mosquito populations and the development of effective vaccines against all four serotypes.

West Nile Fever is defined as a viral infection primarily transmitted to humans through the bite of infected mosquitoes. The virus responsible for this febrile illness, known as West Nile Virus (WNV), is maintained in nature between mosquito vectors and avian hosts. Although most individuals infected with WNV are asymptomatic, some may develop a mild, flu-like illness characterized by fever, headache, fatigue, body aches, skin rash, and swollen lymph glands. A minority of infected individuals, particularly the elderly and immunocompromised, may progress to severe neurological symptoms such as encephalitis (inflammation of the brain), meningitis (inflammation of the membranes surrounding the brain and spinal cord), or acute flaccid paralysis (sudden weakness in the limbs). The diagnosis is confirmed through laboratory tests, such as serological assays or nucleic acid amplification techniques. Treatment primarily focuses on supportive care, as there are no specific antiviral therapies available for West Nile Fever. Preventive measures include personal protection against mosquito bites and vector control strategies to reduce mosquito populations.

Dengue is a mosquito-borne viral infection that is primarily transmitted by the Aedes aegypti and Aedes albopictus species of mosquitoes. It is caused by one of four closely related dengue viruses (DENV 1, DENV 2, DENV 3, or DENV 4). The infection can cause a wide range of symptoms, ranging from mild fever and headache to severe flu-like illness, which is often characterized by the sudden onset of high fever, severe headache, muscle and joint pain, nausea, vomiting, and skin rash. In some cases, dengue can progress to more severe forms, such as dengue hemorrhagic fever or dengue shock syndrome, which can be life-threatening if not treated promptly and appropriately.

Dengue is prevalent in many tropical and subtropical regions around the world, particularly in urban and semi-urban areas with poor sanitation and inadequate mosquito control. There is no specific treatment for dengue, and prevention efforts focus on reducing mosquito populations and avoiding mosquito bites. Vaccines are available in some countries to prevent dengue infection, but they are not widely used due to limitations in their effectiveness and safety.

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.

Japanese Encephalitis Viruses (JEV) are part of the Flaviviridae family and belong to the genus Flavivirus. JEV is the leading cause of viral encephalitis in Asia, resulting in significant morbidity and mortality. The virus is primarily transmitted through the bite of infected Culex mosquitoes, particularly Culex tritaeniorhynchus and Culex vishnui complex.

JEV has a complex transmission cycle involving mosquito vectors, amplifying hosts (primarily pigs and wading birds), and dead-end hosts (humans). The virus is maintained in nature through a enzootic cycle between mosquitoes and amplifying hosts. Humans become infected when bitten by an infective mosquito, but they do not contribute to the transmission cycle.

The incubation period for JEV infection ranges from 5 to 15 days. Most infections are asymptomatic or result in mild symptoms such as fever, headache, and malaise. However, a small percentage of infected individuals develop severe neurological manifestations, including encephalitis, meningitis, and acute flaccid paralysis. The case fatality rate for JEV-induced encephalitis is approximately 20-30%, with up to half of the survivors experiencing long-term neurological sequelae.

There are no specific antiviral treatments available for Japanese encephalitis, and management primarily focuses on supportive care. Prevention strategies include vaccination, personal protective measures against mosquito bites, and vector control programs. JEV vaccines are available and recommended for travelers to endemic areas and for residents living in regions where the virus is circulating.

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.

'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.

Viral envelope proteins are structural proteins found in the envelope that surrounds many types of viruses. These proteins play a crucial role in the virus's life cycle, including attachment to host cells, fusion with the cell membrane, and entry into the host cell. They are typically made up of glycoproteins and are often responsible for eliciting an immune response in the host organism. The exact structure and function of viral envelope proteins vary between different types of viruses.

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.

Cross reactions, in the context of medical diagnostics and immunology, refer to a situation where an antibody or a immune response directed against one antigen also reacts with a different antigen due to similarities in their molecular structure. This can occur in allergy testing, where a person who is allergic to a particular substance may have a positive test result for a different but related substance because of cross-reactivity between them. For example, some individuals who are allergic to birch pollen may also have symptoms when eating certain fruits, such as apples, due to cross-reactive proteins present in both.

Cricetinae is a subfamily of rodents that includes hamsters, gerbils, and relatives. These small mammals are characterized by having short limbs, compact bodies, and cheek pouches for storing food. They are native to various parts of the world, particularly in Europe, Asia, and Africa. Some species are popular pets due to their small size, easy care, and friendly nature. In a medical context, understanding the biology and behavior of Cricetinae species can be important for individuals who keep them as pets or for researchers studying their physiology.

Yellow fever virus (YFV) is an single-stranded RNA virus belonging to the Flaviviridae family, genus Flavivirus. It is primarily transmitted to humans through the bite of infected mosquitoes, most commonly Aedes and Haemagogus species. The virus is named for the jaundice that can occur in some patients, giving their skin and eyes a yellowish color.

Yellow fever is endemic in tropical regions of Africa and South America, with outbreaks occurring when large numbers of people are infected. After an incubation period of 3 to 6 days, symptoms typically begin with fever, chills, headache, back pain, and muscle aches. In more severe cases, the infection can progress to cause bleeding, organ failure, and death.

Prevention measures include vaccination, mosquito control, and personal protective measures such as wearing long sleeves and using insect repellent in areas where yellow fever is endemic or outbreaks are occurring.

Immunoglobulin M (IgM) is a type of antibody that is primarily found in the blood and lymph fluid. It is the first antibody to be produced in response to an initial exposure to an antigen, making it an important part of the body's primary immune response. IgM antibodies are large molecules that are composed of five basic units, giving them a pentameric structure. They are primarily found on the surface of B cells as membrane-bound immunoglobulins (mlgM), where they function as receptors for antigens. Once an mlgM receptor binds to an antigen, it triggers the activation and differentiation of the B cell into a plasma cell that produces and secretes large amounts of soluble IgM antibodies.

IgM antibodies are particularly effective at agglutination (clumping) and complement activation, which makes them important in the early stages of an immune response to help clear pathogens from the bloodstream. However, they are not as stable or long-lived as other types of antibodies, such as IgG, and their levels tend to decline after the initial immune response has occurred.

In summary, Immunoglobulin M (IgM) is a type of antibody that plays a crucial role in the primary immune response to antigens by agglutination and complement activation. It is primarily found in the blood and lymph fluid, and it is produced by B cells after they are activated by an antigen.

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.

Viral nonstructural proteins (NS) are viral proteins that are not part of the virion structure. They play various roles in the viral life cycle, such as replication of the viral genome, transcription, translation regulation, and modulation of the host cell environment to favor virus replication. These proteins are often produced in large quantities during infection and can manipulate or disrupt various cellular pathways to benefit the virus. They may also be involved in evasion of the host's immune response. The specific functions of viral nonstructural proteins vary depending on the type of virus.

St. Louis Encephalitis Virus (SLEV) is a type of arbovirus (arthropod-borne virus) from the family Flaviviridae and genus Flavivirus. It is the causative agent of St. Louis encephalitis (SLE), a viral disease characterized by inflammation of the brain (encephalitis). The virus is primarily transmitted to humans through the bite of infected mosquitoes, particularly Culex spp.

The SLEV infection in humans is often asymptomatic or may cause mild flu-like symptoms such as fever, headache, nausea, and vomiting. However, in some cases, the virus can invade the central nervous system, leading to severe neurological manifestations like meningitis, encephalitis, seizures, and even coma or death. The risk of severe disease increases in older adults and people with weakened immune systems.

There is no specific antiviral treatment for SLE; management typically focuses on supportive care to alleviate symptoms and address complications. Prevention measures include avoiding mosquito bites, using insect repellents, and eliminating breeding sites for mosquitoes. Vaccines are not available for SLEV, but they have been developed and tested in the past, with potential for future use in high-risk populations during outbreaks.

'Culicidae' is the biological family that includes all species of mosquitoes. It consists of three subfamilies: Anophelinae, Culicinae, and Toxorhynchitinae. Mosquitoes are small, midge-like flies that are known for their ability to transmit various diseases to humans and other animals, such as malaria, yellow fever, dengue fever, and Zika virus. The medical importance of Culicidae comes from the fact that only female mosquitoes require blood meals to lay eggs, and during this process, they can transmit pathogens between hosts.

'Culex' is a genus of mosquitoes that includes many species that are vectors for various diseases, such as West Nile virus, filariasis, and avian malaria. They are often referred to as "house mosquitoes" because they are commonly found in urban environments. These mosquitoes typically lay their eggs in standing water and have a cosmopolitan distribution, being found on all continents except Antarctica. The life cycle of Culex mosquitoes includes four stages: egg, larva, pupa, and adult. Both male and female adults feed on nectar, but only females require blood meals to lay eggs.

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.

West Nile Virus (WNV) vaccines are immunizations that are designed to protect against the West Nile virus, which is a single-stranded RNA virus that belongs to the family Flaviviridae. The virus is primarily transmitted to humans through the bite of infected mosquitoes, particularly those of the Culex species.

There are currently no licensed WNV vaccines available for human use in the United States or Europe. However, there are several veterinary vaccines that have been developed and approved for use in horses and other animals, such as birds and geese. These vaccines work by stimulating the immune system to produce antibodies against the virus, which can help prevent infection and reduce the severity of symptoms in animals that do become infected.

Human WNV vaccine candidates are in various stages of development and testing. Some of these vaccines use inactivated or weakened forms of the virus, while others use only a portion of the viral protein to stimulate an immune response. While these vaccines have shown promise in clinical trials, further research is needed to determine their safety and effectiveness in larger populations before they can be approved for widespread use.

St. Louis Encephalitis (SLE) is a type of viral brain inflammation caused by the St. Louis Encephalitis virus. It is transmitted to humans through the bite of infected mosquitoes, primarily Culex species. The virus breeds in warm, stagnant water and is more prevalent in rural and suburban areas.

Most people infected with SLE virus do not develop symptoms or only experience mild flu-like illness. However, some individuals, particularly the elderly, can develop severe illness characterized by sudden onset of fever, headache, neck stiffness, disorientation, coma, seizures, and spastic paralysis. There is no specific treatment for SLE, and management is focused on supportive care, including hydration, respiratory support, and prevention of secondary infections. Vaccination against SLE is not available, and prevention measures include using insect repellent, wearing protective clothing, and eliminating standing water around homes to reduce mosquito breeding sites.

An encyclopedia is a comprehensive reference work containing articles on various topics, usually arranged in alphabetical order. In the context of medicine, a medical encyclopedia is a collection of articles that provide information about a wide range of medical topics, including diseases and conditions, treatments, tests, procedures, and anatomy and physiology. Medical encyclopedias may be published in print or electronic formats and are often used as a starting point for researching medical topics. They can provide reliable and accurate information on medical subjects, making them useful resources for healthcare professionals, students, and patients alike. Some well-known examples of medical encyclopedias include the Merck Manual and the Stedman's Medical Dictionary.

Bacteriophages, often simply called phages, are viruses that infect and replicate within bacteria. They consist of a protein coat, called the capsid, that encases the genetic material, which can be either DNA or RNA. Bacteriophages are highly specific, meaning they only infect certain types of bacteria, and they reproduce by hijacking the bacterial cell's machinery to produce more viruses.

Once a phage infects a bacterium, it can either replicate its genetic material and create new phages (lytic cycle), or integrate its genetic material into the bacterial chromosome and replicate along with the bacterium (lysogenic cycle). In the lytic cycle, the newly formed phages are released by lysing, or breaking open, the bacterial cell.

Bacteriophages play a crucial role in shaping microbial communities and have been studied as potential alternatives to antibiotics for treating bacterial infections.

RNA viruses are a type of virus that contain ribonucleic acid (RNA) as their genetic material, as opposed to deoxyribonucleic acid (DNA). RNA viruses replicate by using an enzyme called RNA-dependent RNA polymerase to transcribe and replicate their RNA genome.

There are several different groups of RNA viruses, including:

1. Negative-sense single-stranded RNA viruses: These viruses have a genome that is complementary to the mRNA and must undergo transcription to produce mRNA before translation can occur. Examples include influenza virus, measles virus, and rabies virus.
2. Positive-sense single-stranded RNA viruses: These viruses have a genome that can serve as mRNA and can be directly translated into protein after entry into the host cell. Examples include poliovirus, rhinoviruses, and coronaviruses.
3. Double-stranded RNA viruses: These viruses have a genome consisting of double-stranded RNA and use a complex replication strategy involving both transcription and reverse transcription. Examples include rotaviruses and reoviruses.

RNA viruses are known to cause a wide range of human diseases, ranging from the common cold to more severe illnesses such as hepatitis C, polio, and COVID-19. Due to their high mutation rates and ability to adapt quickly to new environments, RNA viruses can be difficult to control and treat with antiviral drugs or vaccines.

Vaccinia virus is a large, complex DNA virus that belongs to the Poxviridae family. It is the virus used in the production of the smallpox vaccine. The vaccinia virus is not identical to the variola virus, which causes smallpox, but it is closely related and provides cross-protection against smallpox infection.

The vaccinia virus has a unique replication cycle that occurs entirely in the cytoplasm of infected cells, rather than in the nucleus like many other DNA viruses. This allows the virus to evade host cell defenses and efficiently produce new virions. The virus causes the formation of pocks or lesions on the skin, which contain large numbers of virus particles that can be transmitted to others through close contact.

Vaccinia virus has also been used as a vector for the delivery of genes encoding therapeutic proteins, vaccines against other infectious diseases, and cancer therapies. However, the use of vaccinia virus as a vector is limited by its potential to cause adverse reactions in some individuals, particularly those with weakened immune systems or certain skin conditions.

Virus receptors are specific molecules (commonly proteins) on the surface of host cells that viruses bind to in order to enter and infect those cells. This interaction between the virus and its receptor is a critical step in the infection process. Different types of viruses have different receptor requirements, and identifying these receptors can provide important insights into the biology of the virus and potential targets for antiviral therapies.

Virus cultivation, also known as virus isolation or viral culture, is a laboratory method used to propagate and detect viruses by introducing them to host cells and allowing them to replicate. This process helps in identifying the specific virus causing an infection and studying its characteristics, such as morphology, growth pattern, and sensitivity to antiviral agents.

The steps involved in virus cultivation typically include:

1. Collection of a clinical sample (e.g., throat swab, blood, sputum) from the patient.
2. Preparation of the sample by centrifugation or filtration to remove cellular debris and other contaminants.
3. Inoculation of the prepared sample into susceptible host cells, which can be primary cell cultures, continuous cell lines, or embryonated eggs, depending on the type of virus.
4. Incubation of the inoculated cells under appropriate conditions to allow viral replication.
5. Observation for cytopathic effects (CPE), which are changes in the host cells caused by viral replication, such as cell rounding, shrinkage, or lysis.
6. Confirmation of viral presence through additional tests, like immunofluorescence assays, polymerase chain reaction (PCR), or electron microscopy.

Virus cultivation is a valuable tool in diagnostic virology, vaccine development, and research on viral pathogenesis and host-virus interactions. However, it requires specialized equipment, trained personnel, and biosafety measures due to the potential infectivity of the viruses being cultured.

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