Differential persistence of foot-and-mouth disease virus in African buffalo is related to virus virulence

dc.contributor.authorMaree, Francois Frederick
dc.contributor.authorDe Klerk-Lorist, Lin Mari
dc.contributor.authorGubbins, Simon
dc.contributor.authorZhang, Fuquan
dc.contributor.authorSeago, Julian
dc.contributor.authorPérez-Martín, Eva
dc.contributor.authorReid, Liz
dc.contributor.authorScott, Katherine Anne
dc.contributor.authorVan Schalkwyk, Louis
dc.contributor.authorBengis, Roy G.
dc.contributor.authorCharleston, Bryan
dc.contributor.authorJuleff, Nicholas
dc.date.accessioned2016-07-21T07:24:54Z
dc.date.issued2016-05
dc.description.abstractFoot-and-mouth disease virus (FMDV) circulates as multiple serotypes and strains in many endemic regions. In particular the three Southern African Territories (SAT) serotypes are maintained effectively in their wildlife reservoir, the African buffalo, and individuals may harbour multiple SAT-serotypes for extended periods in the pharyngeal region. However the exact site and mechanism for persistence remain unclear. FMD in buffaloes offers a unique opportunity to study FMDV-persistence, as transmission from carrier ruminants has only convincingly been demonstrated for this species. Following co-infection of naïve African buffaloes with three SAT-serotypes isolated from field buffaloes; palatine tonsil swabs were the sample of choice for recovering infectious FMDV up to 400 days post infection (dpi). Post-mortem examination identified infectious virus for up to 185 dpi and viral genome up to 400 dpi in lymphoid tissue of the head and neck, mainly focussed in germinal centres. Interestingly viral persistence in vivo was not homogenous and the SAT-1 isolate persisted for longer than SAT-2 and SAT-3. Co-infection and passage of these SAT isolates in goat and buffalo cell lines demonstrated a direct correlation between persistence and cell killing capacity. These data suggest FMDV persistence occurs in the germinal centres of lymphoid tissue but the duration of persistence is related to virus replication and cell killing capacity.en_ZA
dc.description.departmentMicrobiology and Plant Pathologyen_ZA
dc.description.embargo2016-11-30
dc.description.librarianhb2016en_ZA
dc.description.sponsorshipNJ was funded as a Wellcome Trust Intermediate Clinical Fellow and funding is acknowledged from the Biotechnology and Biological Sciences Research Council (BBS/E/I/00001523 and BBS/E/I/00001717).en_ZA
dc.description.urihttp://jvi.asm.orgen_ZA
dc.identifier.citationMaree F, de Klerk-Lorist L-M, Gubbins S, Zhang F, Seago J, Pérez-Martín E, Reid L, Scott K, van Schalkwyk L, Bengis R, Charleston B & Juleff N. 2016. Differential persistence of foot-and-mouth disease virus in African buffalo is related to virus virulence. J Virol 90:5132–5140. doi:10.1128/JVI.00166-16.en_ZA
dc.identifier.issn0022-538X (print)
dc.identifier.issn1098-5514 (online)
dc.identifier.other10.1128/JVI.00166-16
dc.identifier.urihttp://hdl.handle.net/2263/56009
dc.language.isoenen_ZA
dc.publisherAmerican Society for Microbiologyen_ZA
dc.rights© 2016, American Society for Microbiology. All Rights Reserved.en_ZA
dc.subjectFoot-and-mouth disease virus (FMDV)en_ZA
dc.subjectDifferential persistenceen_ZA
dc.subjectAfrican buffalo (Syncerus caffer)en_ZA
dc.subjectRelated to virus virulenceen_ZA
dc.subjectSouthern African Territories (SAT)en_ZA
dc.titleDifferential persistence of foot-and-mouth disease virus in African buffalo is related to virus virulenceen_ZA
dc.typePostprint Articleen_ZA

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