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Frontiers in microbiology2016; 7; 1886; doi: 10.3389/fmicb.2016.01886

High Diversity of Genogroup I Picobirnaviruses in Mammals.

Abstract: In a molecular epidemiology study using 791 fecal samples collected from different terrestrial and marine mammals in Hong Kong, genogroup I picobirnaviruses (PBVs) were positive by RT-PCR targeting the partial RdRp gene in specimens from five cattle, six monkeys, 17 horses, nine pigs, one rabbit, one dog, and 12 California sea lions, with 11, 9, 23, 17, 1, 1, and 15 sequence types in the positive specimens from the corresponding animals, respectively. Phylogenetic analysis showed that the PBV sequences from each kind of animal were widely distributed in the whole tree with high diversity, sharing 47.4-89.0% nucleotide identities with other genogroup I PBV strains based on the partial RdRp gene. Nine complete segment 1 (viral loads 1.7 × 10 to 5.9 × 10/ml) and 15 segment 2 (viral loads 4.1 × 10 to 1.3 × 10/ml) of otarine PBVs from fecal samples serially collected from California sea lions were sequenced. In the two phylogenetic trees constructed using ORF2 and ORF3 of segment 1, the nine segment 1 sequences were clustered into four distinct clades (C1-C4). In the tree constructed using RdRp gene of segment 2, the 15 segment 2 sequences were clustered into nine distinct clades (R1-R9). In four sea lions, PBVs were detected in two different years, with the same segment 1 clade (C3) present in two consecutive years from one sea lion and different clades present in different years from three sea lions. A high diversity of PBVs was observed in a variety of terrestrial and marine mammals. Multiple sequence types with significant differences, representing multiple strains of PBV, were present in the majority of PBV-positive samples from different kinds of animals.
Publication Date: 2016-11-23 PubMed ID: 27933049PubMed Central: PMC5120130DOI: 10.3389/fmicb.2016.01886Google Scholar: Lookup
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  • Journal Article

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

The study is about genogroup I picobirnaviruses (PBVs) found in various mammal species in Hong Kong. A significant number of the samples taken from these mammals were positive for PBVs, revealing a high diversity among these viruses.

Research Methods

  • The researchers conducted a molecular epidemiology study where they collected 791 fecal samples from a range of terrestrial and marine mammals in Hong Kong. These included cattle, monkeys, horses, pigs, rabbits, dogs, and California sea lions.
  • They used the RT-PCR technique to target the partial RdRp gene, which is a component of the PBV virus. This method enabled them to identify which samples were PBV positive.
  • They also studied and compared the PBV sequence types found in the positive specimens from each kind of animal.
  • Complete segments of the PBV virus found in the sea lions were sequenced for further analysis.

Results and Findings

  • The study revealed that samples from five cattle, six monkeys, 17 horses, nine pigs, one rabbit, one dog, and 12 California sea lions were positive for PBVs.
  • The analysis of the positive samples showed widely distributed PBV sequences with high diversity. The viral sequences shared 47.4-89.0% nucleotide identities with other strains of genogroup I PBVs based on the partial RdRp gene.
  • Through phylogenetic analysis, the PBV sequences from each animal type were dispersed throughout the entire tree, signifying vast diversity.
  • The PBV sequence types present in the sea lions were clustered into distinct groupings or “clades”.
  • The analysis also revealed the presence of multiple strains of the virus in the majority of PBV-positive samples from the different animals.
  • Four sea lions were found to harbor PBVs in two different years, with the same sequence type (C3) present in two consecutive years in one sea lion, while different types were found in different years in three sea lions.

Conclusion

  • The study concludes that there is a high diversity of PBVs present in a variety of terrestrial and marine mammals in Hong Kong.
  • This highlights the possible complexity and wide distribution of these viruses among different animal hosts, potentially Furthermore, with the finding of multiple virus strains in many of the positive samples, it poses questions regarding the potential viral transmission and infection mechanisms among these animals.

Cite This Article

APA
Woo PC, Teng JL, Bai R, Wong AY, Martelli P, Hui SW, Tsang AK, Lau CC, Ahmed SS, Yip CC, Choi GK, Li KS, Lam CS, Lau SK, Yuen KY. (2016). High Diversity of Genogroup I Picobirnaviruses in Mammals. Front Microbiol, 7, 1886. https://doi.org/10.3389/fmicb.2016.01886

Publication

ISSN: 1664-302X
NlmUniqueID: 101548977
Country: Switzerland
Language: English
Volume: 7
Pages: 1886
PII: 1886

Researcher Affiliations

Woo, Patrick C Y
  • Department of Microbiology, The University of Hong KongHong Kong, China; State Key Laboratory of Emerging Infectious Diseases, The University of Hong KongHong Kong, China; Research Centre of Infection and Immunology, The University of Hong KongHong Kong, China; Carol Yu Centre for Infection, The University of Hong KongHong Kong, China; Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The University of Hong KongHong Kong, China.
Teng, Jade L L
  • Department of Microbiology, The University of Hong KongHong Kong, China; State Key Laboratory of Emerging Infectious Diseases, The University of Hong KongHong Kong, China; Research Centre of Infection and Immunology, The University of Hong KongHong Kong, China; Carol Yu Centre for Infection, The University of Hong KongHong Kong, China.
Bai, Ru
  • Department of Microbiology, The University of Hong Kong Hong Kong, China.
Wong, Annette Y P
  • Department of Microbiology, The University of Hong Kong Hong Kong, China.
Martelli, Paolo
  • Ocean Park Corporation Hong Kong, China.
Hui, Suk-Wai
  • Ocean Park Corporation Hong Kong, China.
Tsang, Alan K L
  • Department of Microbiology, The University of Hong Kong Hong Kong, China.
Lau, Candy C Y
  • Department of Microbiology, The University of Hong Kong Hong Kong, China.
Ahmed, Syed S
  • Department of Microbiology, The University of Hong Kong Hong Kong, China.
Yip, Cyril C Y
  • Department of Microbiology, The University of Hong Kong Hong Kong, China.
Choi, Garnet K Y
  • Department of Microbiology, The University of Hong Kong Hong Kong, China.
Li, Kenneth S M
  • Department of Microbiology, The University of Hong Kong Hong Kong, China.
Lam, Carol S F
  • Department of Microbiology, The University of Hong Kong Hong Kong, China.
Lau, Susanna K P
  • Department of Microbiology, The University of Hong KongHong Kong, China; State Key Laboratory of Emerging Infectious Diseases, The University of Hong KongHong Kong, China; Research Centre of Infection and Immunology, The University of Hong KongHong Kong, China; Carol Yu Centre for Infection, The University of Hong KongHong Kong, China; Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The University of Hong KongHong Kong, China.
Yuen, Kwok-Yung
  • Department of Microbiology, The University of Hong KongHong Kong, China; State Key Laboratory of Emerging Infectious Diseases, The University of Hong KongHong Kong, China; Research Centre of Infection and Immunology, The University of Hong KongHong Kong, China; Carol Yu Centre for Infection, The University of Hong KongHong Kong, China; Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The University of Hong KongHong Kong, China.

References

This article includes 42 references
  1. Attoui H, Billoir F, Cantaloube JF, Biagini P, de Micco P, de Lamballerie X. Strategies for the sequence determination of viral dsRNA genomes.. J Virol Methods 2000 Sep;89(1-2):147-58.
    doi: 10.1016/S0166-0934(00)00212-3pubmed: 10996648google scholar: lookup
  2. Bányai K, Martella V, Bogdán Á, Forgách P, Jakab F, Meleg E, Bíró H, Melegh B, Szűcs G. Genogroup I picobirnaviruses in pigs: evidence for genetic diversity and relatedness to human strains.. J Gen Virol 2008 Feb;89(Pt 2):534-539.
    doi: 10.1099/vir.0.83134-0pubmed: 18198385google scholar: lookup
  3. Bányai K, Potgieter C, Gellért Á, Ganesh B, Tempesta M, Lorusso E, Buonavoglia C, Martella V. Genome sequencing identifies genetic and antigenic divergence of porcine picobirnaviruses.. J Gen Virol 2014 Oct;95(Pt 10):2233-2239.
    doi: 10.1099/vir.0.057984-0pubmed: 24584476google scholar: lookup
  4. Bodewes R, van der Giessen J, Haagmans BL, Osterhaus AD, Smits SL. Identification of multiple novel viruses, including a parvovirus and a hepevirus, in feces of red foxes.. J Virol 2013 Jul;87(13):7758-64.
    doi: 10.1128/JVI.00568-13pmc: PMC3700315pubmed: 23616657google scholar: lookup
  5. Chen M, Sun H, Lan D, Hua X, Cui L, Yuan C, Yang Z. Molecular detection of genogroup I and II picobirnaviruses in pigs in China.. Virus Genes 2014 Jun;48(3):553-6.
    doi: 10.1007/s11262-014-1058-8pubmed: 24682937google scholar: lookup
  6. Da Costa B, Duquerroy S, Tarus B, Delmas B. Picobirnaviruses encode a protein with repeats of the ExxRxNxxxE motif.. Virus Res 2011 Jun;158(1-2):251-6.
  7. de Castro E, Sigrist CJ, Gattiker A, Bulliard V, Langendijk-Genevaux PS, Gasteiger E, Bairoch A, Hulo N. ScanProsite: detection of PROSITE signature matches and ProRule-associated functional and structural residues in proteins.. Nucleic Acids Res 2006 Jul 1;34(Web Server issue):W362-5.
    doi: 10.1093/nar/gkl124pmc: PMC1538847pubmed: 16845026google scholar: lookup
  8. Fregolente MC, de Castro-Dias E, Martins SS, Spilki FR, Allegretti SM, Gatti MS. Molecular characterization of picobirnaviruses from new hosts.. Virus Res 2009 Jul;143(1):134-6.
  9. Ganesh B, Banyai K, Masachessi G, Mladenova Z, Nagashima S, Ghosh S, Nataraju SM, Pativada M, Kumar R, Kobayashi N. Genogroup I picobirnavirus in diarrhoeic foals: can the horse serve as a natural reservoir for human infection?. Vet Res 2011 Mar 17;42(1):52.
    doi: 10.1186/1297-9716-42-52pmc: PMC3068956pubmed: 21414192google scholar: lookup
  10. Ganesh B, Nagashima S, Ghosh S, Nataraju SM, Rajendran K, Manna B, Ramamurthy T, Niyogi SK, Kanungo S, Sur D, Kobayashi N, Krishnan T. Detection and molecular characterization of multiple strains of Picobirnavirus causing mixed infection in a diarrhoeic child: Emergence of prototype Genogroup II-like strain in Kolkata, India.. Int J Mol Epidemiol Genet 2011 Jan 1;2(1):61-72.
    pmc: PMC3077240pubmed: 21537403
  11. Ghosh S, Kobayashi N, Nagashima S, Naik TN. Molecular characterization of full-length genomic segment 2 of a bovine picobirnavirus (PBV) strain: evidence for high genetic diversity with genogroup I PBVs.. J Gen Virol 2009 Oct;90(Pt 10):2519-2524.
    doi: 10.1099/vir.0.013987-0pubmed: 19587136google scholar: lookup
  12. Gillman L, Sánchez AM, Arbiza J. Picobirnavirus in captive animals from Uruguay: identification of new hosts.. Intervirology 2013;56(1):46-9.
    doi: 10.1159/000338275pubmed: 22759924google scholar: lookup
  13. Hofmann H, Pyrc K, van der Hoek L, Geier M, Berkhout B, Pöhlmann S. Human coronavirus NL63 employs the severe acute respiratory syndrome coronavirus receptor for cellular entry.. Proc Natl Acad Sci U S A 2005 May 31;102(22):7988-93.
    doi: 10.1073/pnas.0409465102pmc: PMC1142358pubmed: 15897467google scholar: lookup
  14. Kirkwood CD. Genetic and antigenic diversity of human rotaviruses: potential impact on vaccination programs.. J Infect Dis 2010 Sep 1;202 Suppl:S43-8.
    doi: 10.1086/653548pubmed: 20684716google scholar: lookup
  15. Krogh A, Larsson B, von Heijne G, Sonnhammer EL. Predicting transmembrane protein topology with a hidden Markov model: application to complete genomes.. J Mol Biol 2001 Jan 19;305(3):567-80.
    doi: 10.1006/jmbi.2000.4315pubmed: 11152613google scholar: lookup
  16. Kumar S, Stecher G, Tamura K. MEGA7: Molecular Evolutionary Genetics Analysis Version 7.0 for Bigger Datasets.. Mol Biol Evol 2016 Jul;33(7):1870-4.
    doi: 10.1093/molbev/msw054pmc: PMC8210823pubmed: 27004904google scholar: lookup
  17. Lau SK, Woo PC, Li KS, Huang Y, Tsoi HW, Wong BH, Wong SS, Leung SY, Chan KH, Yuen KY. Severe acute respiratory syndrome coronavirus-like virus in Chinese horseshoe bats.. Proc Natl Acad Sci U S A 2005 Sep 27;102(39):14040-5.
    doi: 10.1073/pnas.0506735102pmc: PMC1236580pubmed: 16169905google scholar: lookup
  18. Lupas A, Van Dyke M, Stock J. Predicting coiled coils from protein sequences.. Science 1991 May 24;252(5009):1162-4.
    doi: 10.1126/science.252.5009.1162pubmed: 2031185google scholar: lookup
  19. Malik YS, Chandrashekar KM, Sharma K, Haq AA, Vaid N, Chakravarti S, Batra M, Singh R, Pandey AB. Picobirnavirus detection in bovine and buffalo calves from foothills of Himalaya and Central India.. Trop Anim Health Prod 2011 Dec;43(8):1475-8.
    doi: 10.1007/s11250-011-9834-0pmc: PMC7088823pubmed: 21479844google scholar: lookup
  20. Malik YS, Kumar N, Sharma K, Sharma AK, Sircar S, Jeena LM. Molecular characterization of a genetically diverse bubaline Picobirnavirus strain, India. Wetchasan Sattawaphaet 39 609–613.
  21. Martínez LC, Masachessi G, Carruyo G, Ferreyra LJ, Barril PA, Isa MB, Giordano MO, Ludert JE, Nates SV. Picobirnavirus causes persistent infection in pigs.. Infect Genet Evol 2010 Oct;10(7):984-8.
    doi: 10.1016/j.meegid.2010.06.004pubmed: 20601172google scholar: lookup
  22. Nates SV, Gatti MSV, Ludert JE. The picobirnavirus: an integrated view on its biology, epidemiology and pathogenic potential. Future Virol 6 223–235.
    doi: 10.2217/fvl.10.76google scholar: lookup
  23. Ng TF, Mesquita JR, Nascimento MS, Kondov NO, Wong W, Reuter G, Knowles NJ, Vega E, Esona MD, Deng X, Vinjé J, Delwart E. Feline fecal virome reveals novel and prevalent enteric viruses.. Vet Microbiol 2014 Jun 25;171(1-2):102-11.
  24. Pereira HG, Fialho AM, Flewett TH, Teixeira JM, Andrade ZP. Novel viruses in human faeces.. Lancet 1988 Jul 9;2(8602):103-4.
    doi: 10.1016/S0140-6736(88)90032-3pubmed: 2898672google scholar: lookup
  25. Pereira HG, Flewett TH, Candeias JA, Barth OM. A virus with a bisegmented double-stranded RNA genome in rat (Oryzomys nigripes) intestines.. J Gen Virol 1988 Nov;69 ( Pt 11):2749-54.
    doi: 10.1099/0022-1317-69-11-2749pubmed: 3053986google scholar: lookup
  26. Ribeiro Silva R, Bezerra DAM, Kaiano JHL, Oliveira DS, Silvestre RVD, Gabbay YB, Ganesh B, Mascarenhas JDP. Genogroup I avian picobirnavirus detected in Brazilian broiler chickens: a molecular epidemiology study.. J Gen Virol 2014 Jan;95(Pt 1):117-122.
    doi: 10.1099/vir.0.054783-0pubmed: 24108140google scholar: lookup
  27. Rosen BI, Fang ZY, Glass RI, Monroe SS. Cloning of human picobirnavirus genomic segments and development of an RT-PCR detection assay.. Virology 2000 Nov 25;277(2):316-29.
    doi: 10.1006/viro.2000.0594pubmed: 11080479google scholar: lookup
  28. Smith GJ, Vijaykrishna D, Bahl J, Lycett SJ, Worobey M, Pybus OG, Ma SK, Cheung CL, Raghwani J, Bhatt S, Peiris JS, Guan Y, Rambaut A. Origins and evolutionary genomics of the 2009 swine-origin H1N1 influenza A epidemic.. Nature 2009 Jun 25;459(7250):1122-5.
    doi: 10.1038/nature08182pubmed: 19516283google scholar: lookup
  29. Smits SL, Schapendonk CM, van Beek J, Vennema H, Schürch AC, Schipper D, Bodewes R, Haagmans BL, Osterhaus AD, Koopmans MP. New viruses in idiopathic human diarrhea cases, the Netherlands.. Emerg Infect Dis 2014 Jul;20(7):1218-22.
    doi: 10.3201/eid2007.140190pmc: PMC4073879pubmed: 24964003google scholar: lookup
  30. Symonds EM, Griffin DW, Breitbart M. Eukaryotic viruses in wastewater samples from the United States.. Appl Environ Microbiol 2009 Mar;75(5):1402-9.
    doi: 10.1128/AEM.01899-08pmc: PMC2648173pubmed: 19124584google scholar: lookup
  31. Vabret A, Mourez T, Gouarin S, Petitjean J, Freymuth F. An outbreak of coronavirus OC43 respiratory infection in Normandy, France.. Clin Infect Dis 2003 Apr 15;36(8):985-9.
    doi: 10.1086/374222pmc: PMC7109673pubmed: 12684910google scholar: lookup
  32. van Leeuwen M, Williams MM, Koraka P, Simon JH, Smits SL, Osterhaus AD. Human picobirnaviruses identified by molecular screening of diarrhea samples.. J Clin Microbiol 2010 May;48(5):1787-94.
    doi: 10.1128/JCM.02452-09pmc: PMC2863890pubmed: 20335418google scholar: lookup
  33. Verma H, Mor SK, Erber J, Goyal SM. Prevalence and complete genome characterization of turkey picobirnaviruses.. Infect Genet Evol 2015 Mar;30:134-139.
  34. Wakuda M, Pongsuwanna Y, Taniguchi K. Complete nucleotide sequences of two RNA segments of human picobirnavirus.. J Virol Methods 2005 Jun;126(1-2):165-9.
  35. Wang Y, Bányai K, Tu X, Jiang B. Simian genogroup I picobirnaviruses: prevalence, genetic diversity, and zoonotic potential.. J Clin Microbiol 2012 Aug;50(8):2779-82.
    doi: 10.1128/JCM.00634-12pmc: PMC3421516pubmed: 22622441google scholar: lookup
  36. Woo PC, Lau SK, Bai R, Teng JL, Lee P, Martelli P, Hui SW, Yuen KY. Complete genome sequence of a novel picobirnavirus, otarine picobirnavirus, discovered in California sea lions.. J Virol 2012 Jun;86(11):6377-8.
    doi: 10.1128/JVI.00686-12pmc: PMC3372223pubmed: 22570247google scholar: lookup
  37. Woo PC, Lau SK, Chu CM, Chan KH, Tsoi HW, Huang Y, Wong BH, Poon RW, Cai JJ, Luk WK, Poon LL, Wong SS, Guan Y, Peiris JS, Yuen KY. Characterization and complete genome sequence of a novel coronavirus, coronavirus HKU1, from patients with pneumonia.. J Virol 2005 Jan;79(2):884-95.
  38. Woo PC, Lau SK, Lam CS, Tsang AK, Hui SW, Fan RY, Martelli P, Yuen KY. Discovery of a novel bottlenose dolphin coronavirus reveals a distinct species of marine mammal coronavirus in Gammacoronavirus.. J Virol 2014 Jan;88(2):1318-31.
    doi: 10.1128/JVI.02351-13pmc: PMC3911666pubmed: 24227844google scholar: lookup
  39. Woo PC, Lau SK, Teng JL, Tsang AK, Joseph M, Wong EY, Tang Y, Sivakumar S, Bai R, Wernery R, Wernery U, Yuen KY. Metagenomic analysis of viromes of dromedary camel fecal samples reveals large number and high diversity of circoviruses and picobirnaviruses.. Virology 2014 Dec;471-473:117-25.
    doi: 10.1016/j.virol.2014.09.020pmc: PMC7112128pubmed: 25461537google scholar: lookup
  40. Yeager CL, Ashmun RA, Williams RK, Cardellichio CB, Shapiro LH, Look AT, Holmes KV. Human aminopeptidase N is a receptor for human coronavirus 229E.. Nature 1992 Jun 4;357(6377):420-2.
    doi: 10.1038/357420a0pmc: PMC7095410pubmed: 1350662google scholar: lookup
  41. Zhang S, Bai R, Feng R, Zhang H, Liu L. Detection and evolutionary analysis of picobirnaviruses in treated wastewater.. Microb Biotechnol 2015 May;8(3):474-82.
    doi: 10.1111/1751-7915.12239pmc: PMC4408179pubmed: 25546400google scholar: lookup
  42. Zhang W, Li L, Deng X, Kapusinszky B, Pesavento PA, Delwart E. Faecal virome of cats in an animal shelter.. J Gen Virol 2014 Nov;95(Pt 11):2553-2564.
    doi: 10.1099/vir.0.069674-0pmc: PMC4202271pubmed: 25078300google scholar: lookup

Citations

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  1. Chauhan RP, San JE, Gordon ML. Metagenomic Analysis of RNA Fraction Reveals the Diversity of Swine Oral Virome on South African Backyard Swine Farms in the uMgungundlovu District of KwaZulu-Natal Province. Pathogens 2022 Aug 17;11(8).
    doi: 10.3390/pathogens11080927pubmed: 36015047google scholar: lookup
  2. Atasoy MO, Isidan H, Turan T. Genetic diversity, frequency and concurrent infections of picobirnaviruses in diarrhoeic calves in Turkey. Trop Anim Health Prod 2022 Mar 5;54(2):127.
    doi: 10.1007/s11250-022-03128-4pubmed: 35247085google scholar: lookup
  3. Folgueiras-González A, van den Braak R, Deijs M, Kuller W, Sietsma S, Thuring V, van der Hoek L, de Groof A. Dynamics of the Enteric Virome in a Swine Herd Affected by Non-PCV2/PRRSV Postweaning Wasting Syndrome. Viruses 2021 Dec 17;13(12).
    doi: 10.3390/v13122538pubmed: 34960807google scholar: lookup
  4. Berg MG, Forberg K, Perez LJ, Luk KC, Meyer TV, Cloherty GA. Emergence of a Distinct Picobirnavirus Genotype Circulating in Patients Hospitalized with Acute Respiratory Illness. Viruses 2021 Dec 17;13(12).
    doi: 10.3390/v13122534pubmed: 34960803google scholar: lookup
  5. Nazaktabar A. Molecular epidemiology and phylogenetic analysis of bovine picobirnaviruses causing calf diarrhea, in Iran. Vet Res Forum 2021;12(3):319-324.
    doi: 10.30466/vrf.2020.110016.2620pubmed: 34815843google scholar: lookup
  6. Huaman JL, Pacioni C, Sarker S, Doyle M, Forsyth DM, Pople A, Hampton JO, Carvalho TG, Helbig KJ. Molecular Epidemiology and Characterization of Picobirnavirus in Wild Deer and Cattle from Australia: Evidence of Genogroup I and II in the Upper Respiratory Tract. Viruses 2021 Jul 29;13(8).
    doi: 10.3390/v13081492pubmed: 34452357google scholar: lookup
  7. Perez LJ, Cloherty GA, Berg MG. Understanding the Genetic Diversity of Picobirnavirus: A Classification Update Based on Phylogenetic and Pairwise Sequence Comparison Approaches. Viruses 2021 Jul 28;13(8).
    doi: 10.3390/v13081476pubmed: 34452341google scholar: lookup
  8. Quiñones B, Yambao JC, De Guzman VS, Lee BG, Medin DL. Genomic analysis of high copy-number sequences for the targeted detection of Listeria species using a flow-through surveillance system. Arch Microbiol 2021 Aug;203(6):3667-3682.
    doi: 10.1007/s00203-021-02388-2pubmed: 34076739google scholar: lookup
  9. Teng JLL, Wernery U, Wong PC, Chan E, Lee HH, Joseph S, Bai R, Tang Y, Wong EYM, Lau SKP, Woo PCY. High Prevalence of Genogroup I and Genogroup II Picobirnaviruses in Dromedary Camels. Viruses 2021 Mar 8;13(3).
    doi: 10.3390/v13030430pubmed: 33800270google scholar: lookup
  10. Mahar JE, Shi M, Hall RN, Strive T, Holmes EC. Comparative Analysis of RNA Virome Composition in Rabbits and Associated Ectoparasites. J Virol 2020 May 18;94(11).
    doi: 10.1128/JVI.02119-19pubmed: 32188733google scholar: lookup
  11. Woo PCY, Teng JLL, Bai R, Tang Y, Wong AYP, Li KSM, Lam CSF, Fan RYY, Lau SKP, Yuen KY. Novel Picobirnaviruses in Respiratory and Alimentary Tracts of Cattle and Monkeys with Large Intra- and Inter-Host Diversity. Viruses 2019 Jun 23;11(6).
    doi: 10.3390/v11060574pubmed: 31234565google scholar: lookup
  12. Knox MA, Gedye KR, Hayman DTS. The Challenges of Analysing Highly Diverse Picobirnavirus Sequence Data. Viruses 2018 Dec 3;10(12).
    doi: 10.3390/v10120685pubmed: 30513931google scholar: lookup
  13. Malik YS, Sircar S, Saurabh S, Kattoor JJ, Singh R, Ganesh B, Ghosh S, Dhama K, Singh RK. Epidemiologic Status of Picobirnavirus in India, A Less Explored Viral Disease. Open Virol J 2018;12:99-109.
    doi: 10.2174/1874357901812010099pubmed: 30288198google scholar: lookup
  14. Kuhar U, Vengust G, Jamnikar-Ciglenecki U. Complete Genome Sequence of Roe Deer Picobirnavirus Strain PBV/roe_deer/SLO/D38-14/2014. Genome Announc 2017 Dec 14;5(50).
    doi: 10.1128/genomeA.01329-17pubmed: 29242222google scholar: lookup
  15. Maan S, Batra K, Rajendhran J, Joseph R, Singh VK, Chaudhary D, Sindhu S, Kadian V, Kumar A, Maan NS, Mor S. Exploring viral diversity in diarrheic porcine feces: a metagenomic analysis from an Indian swine farm. Front Cell Infect Microbiol 2025;15:1653342.
    doi: 10.3389/fcimb.2025.1653342pubmed: 41017909google scholar: lookup
  16. Habuka M, Matsunaga K, Ogawa A, Yaguchi T, Yamamoto S, Tanabe Y. Tsukamurella conjunctivitidis peritonitis diagnosed by 16S rRNA gene sequencing in a patient undergoing peritoneal dialysis. CEN Case Rep 2025 Aug;14(4):553-557.
    doi: 10.1007/s13730-024-00958-zpubmed: 39674841google scholar: lookup