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1.
PLoS One ; 9(4): e94656, 2014.
Article in English | MEDLINE | ID: mdl-24714576

ABSTRACT

Nairobi sheep disease virus (NSDV) of the genus Nairovirus causes a haemorrhagic gastroenteritis in sheep and goats with mortality up to 90%; the virus is found in East and Central Africa, and in India, where the virus is called Ganjam virus. NSDV is closely related to the human pathogen Crimean-Congo haemorrhagic fever virus, which also causes a haemorrhagic disease. As with other nairoviruses, replication of NSDV takes place in the cytoplasm and the new virus particles bud into the Golgi apparatus; however, the effect of viral replication on cellular compartments has not been studied extensively. We have found that the overall structure of the endoplasmic reticulum (ER), the ER-Golgi intermediate compartment and the Golgi were unaffected by infection with NSDV. However, we observed that NSDV infection led to the loss of protein disulphide isomerase (PDI), an oxidoreductase present in the lumen of the endoplasmic reticulum (ER) and which assists during protein folding, from the ER. Further investigation showed that NSDV-infected cells have high levels of PDI at their surface, and PDI is also secreted into the culture medium of infected cells. Another chaperone from the PDI family, ERp57, was found to be similarly affected. Analysis of infected cells and expression of individual viral glycoproteins indicated that the NSDV PreGn glycoprotein is involved in redistribution of these soluble ER oxidoreductases. It has been suggested that extracellular PDI can activate integrins and tissue factor, which are involved respectively in pro-inflammatory responses and disseminated intravascular coagulation, both of which manifest in many viral haemorrhagic fevers. The discovery of enhanced PDI secretion from NSDV-infected cells may be an important finding for understanding the mechanisms underlying the pathogenicity of haemorrhagic nairoviruses.


Subject(s)
Cell Membrane/metabolism , Endoplasmic Reticulum/metabolism , Extracellular Space/metabolism , Nairobi Sheep Disease/metabolism , Nairobi sheep disease virus/physiology , Protein Disulfide-Isomerases/metabolism , Animals , Cell Line , Chlorocebus aethiops , Glycoproteins/metabolism , Goats , Golgi Apparatus/metabolism , Protein Binding , Protein Transport , Vero Cells , Viral Proteins/metabolism , Virus Replication
2.
Indian J Med Res ; 130(5): 514-9, 2009 Nov.
Article in English | MEDLINE | ID: mdl-20090098

ABSTRACT

Ganjam virus (GANV), a member of genus Nairovirus of family Bunyavirdae is of considerable veterinary importance in India. Though, predominantly tick borne, GANV was also isolated from mosquitoes, man and sheep. Neutralizing and complement fixing antibodies to GANV have been detected in animal and human sera collected from different parts of the country. Thirty three strains of GANV have been isolated from India, mainly from Haemaphysalis ticks. The virus replicated in certain vertebrate and mosquito cell lines and found pathogenic to laboratory animals. One natural infection and five laboratory-acquired infections in men were also reported. GANV is antigenically related to Nairobi sheep disease virus (NSDV) of Africa, which is highly pathogenic for sheep and goats causing 70-90 per cent mortality among the susceptible population. Recent molecular studies have demonstrated that GANV is an Asian variant of NSDV and both these viruses are related to the dreaded Crimean Congo haemorrhagic fever (CCHF) group viruses. The versatility of the virus to replicate in different arthropod species, its ability to infect sheep, goat and man makes it an important zoonotic agent.


Subject(s)
Nairobi sheep disease virus/pathogenicity , Animals , Bunyaviridae Infections/transmission , Bunyaviridae Infections/virology , Female , Goats , Humans , India , Male , Mice , Nairobi Sheep Disease/virology , Nairobi sheep disease virus/genetics , Nairobi sheep disease virus/isolation & purification , Nairobi sheep disease virus/physiology , Sheep , Ticks/virology , Virus Replication , Zoonoses/transmission , Zoonoses/virology
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