Genetic diversity and cross-species transmission of kobuviruses in Vietnam

Abstract Cross-species transmission of viruses poses a sustained threat to public health. Due to increased contact between humans and other animal species the possibility exists for cross-species transmissions and ensuing disease outbreaks. By using conventional PCR amplification and next generation sequencing, we obtained 130 partial or full genome kobuvirus sequences from humans in a sentinel cohort in Vietnam and various mammalian hosts including bats, rodents, pigs, cats, and civets. The evolution of kobuviruses in different hosts was analysed using Bayesian phylogenetic methods. We estimated and compared time of origin of kobuviruses in different host orders; we also examined the cross-species transmission of kobuviruses within the same host order and between different host orders. Our data provide new knowledge of rodent and bat kobuviruses, which are most closely related to human kobuviruses. The novel bat kobuviruses isolated from bat roosts in Southern Vietnam were genetically distinct from previously described bat kobuviruses, but closely related to kobuviruses found in rodents. We additionally found evidence of frequent cross-species transmissions of kobuviruses within rodents. Overall, our phylogenetic analyses reveal multiple cross-species transmissions both within and among mammalian species, which increases our understanding of kobuviruses genetic diversity and the complexity of their evolutionary history.

[1]  D. Jongsomjit,et al.  Unique genome organization of non-mammalian papillomaviruses provides insights into the evolution of viral early proteins , 2017, Virus evolution.

[2]  P. Simmonds,et al.  Characterization of Posa and Posa-like virus genomes in fecal samples from humans, pigs, rats, and bats collected from a single location in Vietnam , 2017, Virus evolution.

[3]  J. Farrar,et al.  Large-scale screening and characterization of enteroviruses and kobuviruses infecting pigs in Vietnam. , 2016, The Journal of general virology.

[4]  P. Simmonds,et al.  Evolution and phylogeographic dissemination of endemic porcine picornaviruses in Vietnam , 2016, Virus evolution.

[5]  E. Delwart,et al.  Novel picornavirus in domestic rabbits (Oryctolagus cuniculus var. domestica) , 2015, Infection, Genetics and Evolution.

[6]  S. Baker,et al.  The baseline characteristics and interim analyses of the high-risk sentinel cohort of the Vietnam Initiative on Zoonotic InfectiONS (VIZIONS) , 2015, Scientific Reports.

[7]  J. Farrar,et al.  The Vietnam Initiative on Zoonotic Infections (VIZIONS): A Strategic Approach to Studying Emerging Zoonotic Infectious Diseases , 2015, EcoHealth.

[8]  C. Feschotte,et al.  Cross-Species Transmission and Differential Fate of an Endogenous Retrovirus in Three Mammal Lineages , 2015, bioRxiv.

[9]  W. Ian Lipkin,et al.  Detection of Zoonotic Pathogens and Characterization of Novel Viruses Carried by Commensal Rattus norvegicus in New York City , 2014, mBio.

[10]  G. Reuter,et al.  Identification and complete genome analysis of kobuvirus in faecal samples of European roller (Coracias garrulus): for the first time in a bird , 2014, Archives of Virology.

[11]  J. Oem,et al.  Novel Kobuvirus species identified from black goat with diarrhea. , 2014, Veterinary microbiology.

[12]  J. Farrar,et al.  Prevalence, genetic diversity and recombination of species G enteroviruses infecting pigs in Vietnam. , 2014, The Journal of general virology.

[13]  Derrick E. Wood,et al.  Kraken: ultrafast metagenomic sequence classification using exact alignments , 2014, Genome Biology.

[14]  S. Powell They Eat What? A Cultural Encyclopedia of Weird and Exotic Food from around the World , 2013 .

[15]  Anton J. Enright,et al.  Kraken: A set of tools for quality control and analysis of high-throughput sequence data , 2013, Methods.

[16]  B. Haagmans,et al.  Metagenomic Analysis of the Ferret Fecal Viral Flora , 2013, PloS one.

[17]  S. Rutjes,et al.  Aichi Virus in Sewage and Surface Water, the Netherlands , 2013, Emerging infectious diseases.

[18]  J. Epstein,et al.  Bats are a major natural reservoir for hepaciviruses and pegiviruses , 2013, Proceedings of the National Academy of Sciences.

[19]  M. Suchard,et al.  Improving the accuracy of demographic and molecular clock model comparison while accommodating phylogenetic uncertainty. , 2012, Molecular biology and evolution.

[20]  Rachel L. Marine,et al.  High Variety of Known and New RNA and DNA Viruses of Diverse Origins in Untreated Sewage , 2012, Journal of Virology.

[21]  Shuyi Zhang,et al.  Virome Analysis for Identification of Novel Mammalian Viruses in Bat Species from Chinese Provinces , 2012, Journal of Virology.

[22]  S. Olabarriaga,et al.  Performance of VIDISCA-454 in Feces-Suspensions and Serum , 2012, Viruses.

[23]  E. Kalko,et al.  Bats Worldwide Carry Hepatitis E Virus-Related Viruses That Form a Putative Novel Genus within the Family Hepeviridae , 2012, Journal of Virology.

[24]  M. Suchard,et al.  Bayesian Phylogenetics with BEAUti and the BEAST 1.7 , 2012, Molecular biology and evolution.

[25]  T. Heidmann,et al.  Ancestral capture of syncytin-Car1, a fusogenic endogenous retroviral envelope gene involved in placentation and conserved in Carnivora , 2012, Proceedings of the National Academy of Sciences.

[26]  M. Knörnschild,et al.  Bats host major mammalian paramyxoviruses , 2012, Nature Communications.

[27]  P. Simmonds SSE: a nucleotide and amino acid sequence analysis platform , 2012, BMC Research Notes.

[28]  R. K. Rose,et al.  The Fecal Viral Flora of Wild Rodents , 2011, PLoS pathogens.

[29]  P. Simmonds,et al.  Characterization of a Canine Homolog of Human Aichivirus , 2011, Journal of Virology.

[30]  R. Drury Hungry for success: Urban consumer demand for wild animal products in Vietnam , 2011 .

[31]  C. Rice,et al.  Characterization of a canine homolog of hepatitis C virus , 2011, Proceedings of the National Academy of Sciences.

[32]  Marcel Martin Cutadapt removes adapter sequences from high-throughput sequencing reads , 2011 .

[33]  Angela C. M. Luyf,et al.  UvA-DARE ( Digital Academic Repository ) A Sensitive Assay for Virus Discovery in Respiratory Clinical Samples , 2011 .

[34]  G. Reuter,et al.  Kobuviruses – a comprehensive review , 2011, Reviews in medical virology.

[35]  G. Reuter,et al.  Kobuvirus in Domestic Sheep, Hungary , 2010, Emerging infectious diseases.

[36]  Aize Kijlstra,et al.  Rodent-borne diseases and their risks for public health , 2009, Critical reviews in microbiology.

[37]  G. Reuter,et al.  Candidate New Species of Kobuvirus in Porcine Hosts , 2008, Emerging infectious diseases.

[38]  P. Khamrin,et al.  Sequence analysis of the capsid gene of Aichi viruses detected from Japan, Bangladesh, Thailand, and Vietnam , 2008, Journal of medical virology.

[39]  O. Pybus,et al.  Correlating viral phenotypes with phylogeny: accounting for phylogenetic uncertainty. , 2008, Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases.

[40]  Rodrigo Lopez,et al.  Clustal W and Clustal X version 2.0 , 2007, Bioinform..

[41]  H. Field,et al.  Bats: Important Reservoir Hosts of Emerging Viruses , 2006, Clinical Microbiology Reviews.

[42]  J. Gonzalez,et al.  Fruit bats as reservoirs of Ebola virus , 2005, Nature.

[43]  Mark E.J. Woolhouse,et al.  Host Range and Emerging and Reemerging Pathogens , 2005, Emerging infectious diseases.

[44]  Pius Chilonda,et al.  Geographical determinants and environmental implications of livestock production intensification in Asia. , 2005, Bioresource technology.

[45]  J. Cooper Wildlife species for sustainable food production , 1995, Biodiversity & Conservation.

[46]  T. Yamashita,et al.  Isolation and characterization of a new species of kobuvirus associated with cattle. , 2003, The Journal of general virology.

[47]  M. Stanhope,et al.  Rodent phylogeny and a timescale for the evolution of Glires: evidence from an extensive taxon sampling using three nuclear genes. , 2002, Molecular biology and evolution.

[48]  M E Woolhouse,et al.  Risk factors for human disease emergence. , 2001, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[49]  H. Field,et al.  Nipah virus infection in bats (order Chiroptera) in peninsular Malaysia. , 2001, Emerging infectious diseases.

[50]  S. Yamazaki,et al.  Complete Nucleotide Sequence and Genetic Organization of Aichi Virus, a Distinct Member of the PicornaviridaeAssociated with Acute Gastroenteritis in Humans , 1998, Journal of Virology.

[51]  R. Krause,et al.  Dynamics of emergence. , 1994, The Journal of infectious diseases.

[52]  T. Yamashita,et al.  Isolation of cytopathic small round viruses with BS-C-1 cells from patients with gastroenteritis. , 1991, The Journal of infectious diseases.

[53]  D. W. Morrison Bat ecology. , 1983, Science.