Wikipedia

Cache Valley orthobunyavirus

Cache Valley orthobunyavirus (CVV) is a member of the order Bunyavirales, genus Orthobunyavirus, and serogroup Bunyamwera, which was first isolated in 1956 from Culiseta inornata mosquitos collected in Utah's Cache Valley.[1] CVV is an enveloped arbovirus, nominally 80–120 nm in diameter, whose genome is composed of three single-stranded, negative-sense RNA segments.[1][2] The large segment of related bunyaviruses is approximately 6800 bases in length and encodes a probable viral polymerase.[1] The middle CVV segment has a 4463-nucleotide sequence and the smallest segment encodes for the nucleocapsid, and a second non-structural protein.[1] CVV has been known to cause outbreaks of spontaneous abortion and congenital malformations in ruminants such as sheep and cattle. CVV rarely infects humans, but when they are infected it has caused encephalitis and multiorgan failure.[3]

Cache Valley orthobunyavirus
Virus classification Edit this classification
(unranked): Virus
Realm: Riboviria
Kingdom: Orthornavirae
Phylum: Negarnaviricota
Class: Ellioviricetes
Order: Bunyavirales
Family: Peribunyaviridae
Genus: Orthobunyavirus
Species:
Cache Valley orthobunyavirus
Synonyms
  • Cache Valley virus

Virology

edit

Genome

edit

The Cache Valley virus genome is split into three parts.[4] The three parts are called the small, medium, and large segments, based on the number of bases. The large segment encodes the L protein, which is the RNA dependent RNA polymerase. The small segment utilizes an open reading frame with alternative initiation sites to encode two proteins. Depending on the initiation site, it can either code for the protein that makes up the nucleocapsid, N, or a non-structural protein, NSs.[5] The medium segment encodes 2 type 1 integral transmembrane glycoproteins, Gn and Gc, as well as a non-structural protein Nsm. The Gc and Gn proteins start as one precursor protein and are then cleaved cotranslationally. They are modified by N-linked glycosylation.[6]

Replication cycle

edit

The attachment, entry, replication, and release of CVV specifically have not been studied. However, there is information of the replication cycle for the genus orthobunyavirus, which CVV is a part of. A heterodimer of integral transmembrane proteins Gn and Gc form spikes on the surface of the virus particle. They are involved in virus attachment and cell fusion.[7] Once inside the cell, the viral membrane fuses with the endosomal membrane, and the virus genome is released. Transcription involves an RNA dependent RNA polymerase, and it occurs in the cytoplasm of the cell. Transcription of the tripartite genome is terminated by a strong hairpin loop sequence at the end of each segment. Once the virus has replicated enough, it is encapsidated.[8] Assembly and budding of the newly synthesized virions occurs at the membranes of the Golgi apparatus.[9]

Host interactions

edit

In terms of CVV alone, very little is known about the regulation of host-processes and interactions with host cells. However, CVVs Bunyamwera serogroup's two non-structural proteins play an important role in infection. Bunyamwera virus (BUNV) codes for two non-structural proteins: NSm on the medium RNA segment and NSs on the smallest RNA segment.[10] Bunyamwera virus NSs protein is a nonessential gene that contributes to viral pathogenesis. It has been shown that in mammalian cells, NSs induces shut-off of host protein synthesis, which leads to cell death.[10] It also counteracts the host cell antiviral response and seems to be the main virulence factor,[11] acting at the level of transcription by inhibiting RNA polymerase II–mediated transcription.[12] In mosquito cells neither host cell transcription nor translation are inhibited,[13] and although so far no function for the orthobunyavirus NSs protein has been found in mosquito cells,[14] it seems the differential behavior of NSs could be one of the factors responsible for different outcomes of infection in mammalian and mosquito cell lines.[10]

Human cases

edit

Prior to 1956 there were no known cases of acute infections of Cache Valley virus (CVV) in humans. However antibodies against CVV have been reported.[15] One study found neutralizing antibody to CVV in 12% of 356 persons surveyed in Maryland and Virginia in the 1960s. These results and other such serosurveys are based on nonrandom sampling and therefore often difficult to interpret.[16]

CVV disease is a neuroinvasive illness.[16] Of the three confirmed human cases of CVV disease two resulted in non-fatal meningitis, only the first case caused fatal encephalitis and multiorgan failure.

The first case was a 28-year-old man from North Carolina in 1995. It is likely he was infected with the virus via mosquitos during a deer-hunting trip. The patient's first symptoms were muscle pain, fever, chills and a headache. He began vomiting the day after the first symptoms appeared. Six days after the onset of the illness more severe symptoms appeared including confusion, tachycardia (elevated heart rate), a rash, bilateral conjunctivitis and meningismus. The next day the patient became hypotensive and delirious. Later respiratory failure, seizures and necrosis of the fingers and toes occurred. One leg was amputated because of extensive muscle and cutaneous necrosis. Seven months after the onset of the illness the patient died of pulmonary complications. The causative agent was identified as a virus in the family Bunyaviridae by electron microscopy. This was then identified genetically as CVV. Viremia was recorded seven days after the onset of fever; this is a longer period of viremia than what is normally observed in cases of Bunyaviridae infections.[15]

The second human case of CVV was a 41-year-old man from Wisconsin in October 2003. He developed an acute illness with severe nausea, vomiting, fatigue and headache. He was diagnosed with acute aseptic meningitis. After three days the patient was released from the hospital; he reported feeling fully recovered four months later, though he experienced headaches more frequently than usual. The causative agent was observed with electron microscopy as being virions morphologically similar to bunyaviruses. Nucleotide sequencing identified the virus as CVV.[16]

The third human case of CVV was a 63-year-old woman in New York, in September 2011. When she was admitted to the hospital her symptoms were fever, headache, neck stiffness and photophobia. A week before she had noticed a lesion on her arm, as this began to fade a rash developed and spread. She then developed a fever and symptoms of meningitis. The patient was discharged, but returned the next day with nausea and vomiting. She was diagnosed with aseptic meningitis. She was discharged four days later. Two months after this she reported ongoing difficulties in word finding and headaches. CVV was identified as the causative agent by PCR, sequence analysis confirmed this identification.[4]

It is likely that CVV disease is underreported. Very few human cases have been reported despite its wide geographic distribution and the large number of mosquito species that transmit it.[4] The rarity of CVV disease diagnosis is partly due to the fact that laboratories rarely test for CVV. Therefore, the true incidence of CVV disease and its full clinical range are still unknown.[16] Given the widespread distribution of CVV and other viruses in the same serogroup in the United States it is possible some unexplained cases of severe multiorgan failure, congenital anomalies and human viral encephalitis may be due to CVV or similar viruses. More research of such cases is needed.[15]

Other animals

edit

Cache Valley virus is the most common Orthobunyavirus in North America,[17] and while isolated in 1956, was only linked to disease in Texas in 1987 during a large occurrence of aborted and malformed lambs in a sheep flock.[18] The virus does not only infect sheep, however, as In 2002 a survey conducted in 22 states showed 28% of cattle expressed specific antibodies to CVV.[19] Cache Valley virus has also been identified as a cause of fetal abnormalities in goats.[20] Other serological surveys have also shown antibodies to CVV in domestic and wild ruminants, along with horses. Of wild ruminants, deer have a very high seroprevalence. With viraemia lasting 1 to 3 days, they are easily able to spread the virus to vectors including Culicoides midges and Aedes, Anopheles, Coquillettidia and Culiseta group mosquitoes. Therefore, deer tend to act as amplifying hosts to the virus.[17]

Symptoms in sheep

edit

While the virus is able to replicate in adult animals, besides a slight febrile response in some cases, there are no known symptoms of infection.[17][21] There is a quick period of viraemia before seroconversion and the infection is cleared quickly by the animal's immune system.[21] However, if the animal is pregnant and not protected by antibodies from a previous infection, Cache Valley virus can be very lethal to a developing fetus.[21]

The symptoms the fetus develops from CVV infection are largely age dependent. At less than 28 days of gestation, the embryo usually dies and is reabsorbed by the mother.[22] Between 28 and 45 days of gestation, infection leads to malformations in the developing fetus and occasionally leads to abortions. Early in this window, between 28 and 36 days, the virus leads to both central nervous system and musculoskeletal defects, while after 36 days of gestation infection only leads to musculoskeletal deformities.[17] Death of the fetus usually occurs between 27 and 35 days gestation, when the central nervous system tissues are most susceptible.[17] After 45–50 days of gestation CVV infection is not expected to cause harmful effects.[22] After 76 days the fetus has a functioning immune system and antibodies to the virus are produced.[17]

Autopsies of infected fetuses show severe lesions in the brain and spinal column, ranging from microscopic in size to whole sections of the brain missing.[17][21] In one laboratory case, the cerebral hemispheres were nothing more than fluid-filled sacs that were easily ruptured.[23] The most common musculoskeletal deformations include arthrogryposis and greatly reduced muscle mass, with the most severe cases having torticollis, scoliosis, and kyphosis.[23] While most affected lambs are stillborn, those that do survive are usually so weak they die within minutes of birth.[24] During the time that they are alive, these lamb are reported to act abnormal, such as acting weak, drowsy, or walking unsteadily.[25]

Pathology

edit

When ewes were experimentally infected with Akabane virus, a teratogenic virus of the genus Orthobunyavirus closely related to Cache Valley virus, the virus was shown to replicate in the trophoblastic cells of the placenta. When the virus crossed the placenta and infected the developing fetus, it showed a tropism for the immature fetal cells of the central nervous system and skeletal muscle.[21] Hydranencephaly has also been identified in goat kids with presumptive in utero infection with Cache Valley virus.[20]

History

edit

Cache Valley virus was first isolated from mosquitoes in Utah in 1956.[26] It derives its name from Cache Valley, an agricultural valley located in northern Utah and southeast Idaho. It is endemic to North America, specifically Canada, Mexico, and the United States.[21] The first confirmed human case happened on November 2, 1995. In Texas in 1987, CVV was described as a possible causative agent of disease in sheep.[18] The white-tailed deer population has been identified as a potential natural reservoir.[4]

Prevention

edit

Currently, there is no vaccine or known treatment available for CVV.[27] The most effective method of protecting ruminants from CVV is to minimize their exposure to mosquito-infested areas during and shortly after breeding season.[27] Concerning the safety of humans, it is advised that necessary precautions be taken, such as, putting on mosquito repellent or layers of clothing, when being exposed to mosquito-infested areas.

References

edit
  1. ^ a b c d Grimstad, P. (2001). "Cache Valley virus". In Ashford, R.W. (ed.). Encyclopedia of Arthropod-transmitted Infections of Man and Domesticated Animals. CABI. pp. 101–4. ISBN 9781845933166.
  2. ^ Sims, R. (30 December 2009). "Can Cache Valley virus trash your manufacturing?".
  3. ^ Cache Valley virus. (2012). http://medical-dictionary.thefreedictionary.com/Cache Valley virus.
  4. ^ a b c d Nguyen NL, Zhao G, Hull R, Shelly MA, Wong SJ, Wu G, St George K, Wang D, Menegus MA (June 2013). "Cache valley virus in a patient diagnosed with aseptic meningitis". J Clin Microbiol. 51 (6): 1966–9. doi:10.1128/JCM.00252-13. PMC 3716113. PMID 23515536.
  5. ^ Obijeski JF, Murphy FA (October 1977). "Bunyaviridae: recent biochemical developments". J Gen Virol. 37 (1): 1–14. doi:10.1099/0022-1317-37-1-1. PMID 335022.
  6. ^ Shi X, Kohl A, Li P, Elliott RM (September 2007). "Role of the cytoplasmic tail domains of Bunyamwera orthobunyavirus glycoproteins Gn and Gc in virus assembly and morphogenesis". J Virol. 81 (18): 10151–60. doi:10.1128/JVI.00573-07. PMC 2045389. PMID 17609275.
  7. ^ Shi X, Goli J, Clark G, Brauburger K, Elliott RM (October 2009). "Functional analysis of the Bunyamwera orthobunyavirus Gc glycoprotein". J Gen Virol. 90 (10): 2483–2492. doi:10.1099/vir.0.013540-0. PMC 2885756. PMID 19570952.
  8. ^ Orthobunyavirus (n.d.). In Viral Zone. Retrieved from http://viralzone.expasy.org/all_by_species/250.html
  9. ^ Shi X, van Mierlo JT, French A, Elliott RM (September 2010). "Visualizing the replication cycle of bunyamwera orthobunyavirus expressing fluorescent protein-tagged Gc glycoprotein". J Virol. 84 (17): 8460–9. doi:10.1128/JVI.00902-10. PMC 2919021. PMID 20573824.
  10. ^ a b c Szemiel AM, Failloux AB, Elliott RM (2012). "Role of Bunyamwera Orthobunyavirus NSs protein in infection of mosquito cells". PLOS Negl Trop Dis. 6 (9): e1823. doi:10.1371/journal.pntd.0001823. PMC 3459826. PMID 23029584.
  11. ^ Kohl A, Clayton RF, Weber F, Bridgen A, Randall RE, Elliott RM (July 2003). "Bunyamwera virus nonstructural protein NSs counteracts interferon regulatory factor 3-mediated induction of early cell death". J Virol. 77 (14): 7999–8008. doi:10.1128/jvi.77.14.7999-8008.2003. PMC 161919. PMID 12829839.
  12. ^ Thomas D, Blakqori G, Wagner V, Banholzer M, Kessler N, Elliott RM, Haller O, Weber F (July 2004). "Inhibition of RNA polymerase II phosphorylation by a viral interferon antagonist". J Biol Chem. 279 (30): 31471–7. doi:10.1074/jbc.M400938200. PMID 15150262.
  13. ^ Hart TJ, Kohl A, Elliott RM (August 2009). "Role of the NSs protein in the zoonotic capacity of Orthobunyaviruses". Zoonoses Public Health. 56 (6–7): 285–96. doi:10.1111/j.1863-2378.2008.01166.x. PMID 18771514. S2CID 25312245.
  14. ^ Blakqori G, Delhaye S, Habjan M, Blair CD, Sánchez-Vargas I, Olson KE, Attarzadeh-Yazdi G, Fragkoudis R, Kohl A, Kalinke U, Weiss S, Michiels T, Staeheli P, Weber F (May 2007). "La Crosse bunyavirus nonstructural protein NSs serves to suppress the type I interferon system of mammalian hosts". J Virol. 81 (10): 4991–9. doi:10.1128/JVI.01933-06. PMC 1900204. PMID 17344298.
  15. ^ a b c Sexton DJ, Rollin PE, Breitschwerdt EB, Corey GR, Myers SA, Dumais MR, Bowen MD, Goldsmith CS, Zaki SR, Nichol ST, Peters CJ, Ksiazek TG (February 1997). "Life-threatening Cache Valley virus infection". N Engl J Med. 336 (8): 547–9. doi:10.1056/NEJM199702203360804. PMID 9023091.
  16. ^ a b c d Campbell GL, Mataczynski JD, Reisdorf ES, Powell JW, Martin DA, Lambert AJ, Haupt TE, Davis JP, Lanciotti RS (May 2006). "Second human case of Cache Valley virus disease". Emerg Infect Dis. 12 (5): 854–6. doi:10.3201/eid1205.051625. PMC 3374447. PMID 16704854.
  17. ^ a b c d e f g International Office of Epizootics (2012). "Bunyaviral Diseases of Animals (excluding Rift Valley fever and Crimean—Congo haemorrhagic fever)". Manual of diagnostic tests and vaccines for terrestrial animals: (mammals, birds and bees). Vol. 2 (7th ed.). Office international des épizooties. pp. 2–4. ISBN 9789290448808. OCLC 914567638.
  18. ^ a b Chung SI, Livingston CW, Edwards JF, Crandell RW, Shope RE, Shelton MJ, Collisson EW (February 1990). "Evidence that Cache Valley virus induces congenital malformations in sheep". Vet Microbiol. 21 (4): 297–307. doi:10.1016/0378-1135(90)90001-c. PMID 2107620.
  19. ^ Sahu SP, Pedersen DD, Ridpath HD, Ostlund EN, Schmitt BJ, Alstad DA (July 2002). "Serologic survey of cattle in the northeastern and north central United States, Virginia, Alaska, and Hawaii for antibodies to Cache Valley and antigenically related viruses (Bunyamwera serogroup virus)". Am J Trop Med Hyg. 67 (1): 119–22. doi:10.4269/ajtmh.2002.67.119. PMID 12363055. S2CID 39239621.
  20. ^ a b Harvey J, Smith J, Jackson N, Kreuder A, Dohlman T, Smith J (2019). "Cache Valley virus as a cause of fetal abnormalities in a litter of three Boer kids". Vet Rec Case Rep. 7 (1): e000725. doi:10.1136/vetreccr-2018-000725. S2CID 92700815.
  21. ^ a b c d e f Zeller H, Bouloy M (April 2000). "Infections by viruses of the families Bunyaviridae and Filoviridae". Rev Sci Tech. 19 (1): 79–91. doi:10.20506/rst.19.1.1208. PMID 11189728.
  22. ^ a b Schoenian, S. (n.d.). Sheep 201: Sheep diseases A–Z. Retrieved December 5, 2014, from http://www.sheep101.info/201/diseasesa-z.html
  23. ^ a b Edwards JF, Livingston CW, Chung SI, Collisson EC (January 1989). "Ovine arthrogryposis and central nervous system malformations associated with in utero Cache Valley virus infection: spontaneous disease". Vet Pathol. 26 (1): 33–9. doi:10.1177/030098588902600106. PMID 2492399. S2CID 20357128.
  24. ^ Redden, R., & Dyer, N. (2011, January 13). Cache Valley Virus May Have Affected N.D. Sheep (E. Crawford, Ed.). Retrieved December 6, 2014, from http://www.ag.ndsu.edu/news/newsreleases/2011/jan-10-2011/cache-valley-virus-may-have-affected-n-d-sheep
  25. ^ "Mosquito-spread virus affecting lamb crop | Pipestone County Star". Pipestone County Star. 16 February 2011.
  26. ^ Goldsmith CS, Ksiazek TG, Rollin PE, Comer JA, Nicholson WL, Peret TC, Erdman DD, Bellini WJ, Harcourt BH, Rota PA, Bhatnagar J, Bowen MD, Erickson BR, McMullan LK, Nichol ST, Shieh WJ, Paddock CD, Zaki SR (June 2013). "Cell culture and electron microscopy for identifying viruses in diseases of unknown cause". Emerg Infect Dis. 19 (6): 886–91. doi:10.3201/eid1906.130173. PMC 3713842. PMID 23731788.
  27. ^ a b Hannaway N. (2014). Cache Valley Virus showing up in Ohio sheep. Ohio’s Country Journal: 1.
Retrieved from "https://en.wiki.x.io/w/index.php?title=Cache_Valley_orthobunyavirus&oldid=1188027025"