Document Type : Original Article

Author

Department of Pathobiology, Faculty of Veterinary Medicine, Amol University of Special Modern Technologies, Amol, Iran

Abstract

Picobirnavirus (PBV) is an enteropathogen virus causing diarrhea as an opportunistic virus in its vertebrate host. There is no information about human or animal PBVs in Iran. The aim of the present study was the investigation of the epidemiology of bovine PBV in the broad geographical area of Iran. Four hundred and eighty-five stool samples of up to 1 month old diarrheic calves were collected from 14 provinces and were tested with polyacrylamide gel electrophoresis (PAGE), and reverse transcription polymerase chain reaction (RT-PCR). Five samples were positive in PAGE assay (1.00%) and all of them were amplified using GI specific primers in RT-PCR. Phylogenetic analysis of one of the amplicons (strain Nazaktabar-14) revealed a low relationship to bovine PBV sequences and more identity to PBV isolates from other hosts. The structural alignment of the deduced amino acids of the partially sequenced RdRp gene of the Nazaktabar-14 strain showed high conservation. Sequences obtained from other amplicons showed a high mutation rate and further analysis of one of them showed that, despite the potential of forming deleterious mutations, most of the point mutations occurred in the RdRp gene of PBVs may be a silent mutation. There is little information about the molecular epidemiology of bovine PBVs. This study was the first report on the occurrence of PBVs in Iran and the first study on the molecular epidemiology of bovine PBV in the Middle East, revealing its low frequency as a diarrhea causative agent.

Keywords

  1. Delmas B, Attoui H, Ghosh S, et al. ICTV virus taxonomy profile: Picobirnaviridae. J Gen Virol 2019;100(2):133-134.
  2. Ganesh B, Masachessi G, Mladenova Z. Animal picobirnavirus. Virusdisease 2014;25(2):223-238.
  3. Malik YS, Kumar N, Sharma K, et al. Epidemiology, phylogeny, and evolution of emerging enteric picobirnaviruses of animal origin and their relationship to human strains. BioMed Res Int 2014;2014:780752. doi: 10.1155/2014/780752.
  4. Wakuda M, Pongsuwanna Y, Taniguchi K. Complete nucleotide sequences of two RNA segments of human picobirnavirus. J Virol Methods 2005;126(1-2):165-169.
  5. Rosen BI, Fang Z Y, Glass RI, et al. Cloning of human picobirnavirus genomic segments and development of an RT-PCR detection assay. Virology 2000;277 (2):316-329.
  6. Pereira HG, Fialho AM, Flewett TH, et al. Novel viruses in human faeces. Lancet 1988; 332(8602):103-104.
  7. Pereira HG, Flewett TH, Candeias JA, et al. A virus with a bisegmented double-stranded RNA genome in rat (Oryzomys nigripes) intestines. J Gen Virol 1988;69(Pt 11):2749-2754.
  8. Masachessi G, Martínez LC, Giordano MO, et al. Picobirnavirus (PBV) natural hosts in captivity and virus excretion pattern in infected animals. Arch Virol 2007;152(5):989-998.
  9. Fregolente MCD, de Castro-Dias E, Martins SS, et al. Molecular characterization of picobirnaviruses from new hosts. Virus Res 2009;143(1):134-136.
  10. Masachessi G, Martinez LC, Ganesh B, et al. Establishment and maintenance of persistent infection by picobirnavirus in greater rhea (Rhea Americana). Arch Virol 2012;157(11):2075-2082.
  11. Masachessi G, Ganesh B, Martinez LC, et al. Maintenance of picobirnavirus (PBV) infection in an adult orangutan (Pongo pygmaeus) and genetic diversity of excreted viral strains during a three-year period. Infect Genet Evol 2015;29:196-202.
  12. Malik YS, Chandrashekar KM, Sharma K, et al. Picobirnavirus detection in bovine and buffalo calves from foothills of Himalaya and Central India. Trop Anim Health Prod 2011;43:1475-1478.
  13. Hamza IA, Jurzik L, Uberla K, et al. Evaluation of pepper mild mottle virus, human picobirnavirus and Torque teno virus as indicators of fecal contamination in river water. Water Res 2011;45(3):1358-1368.
  14. Krishnamurthy SR, Wang D. Extensive conservation of prokaryotic ribosomal binding sites in known and novel picobirnaviruses. Virology. 2018;516:108-114.
  15. Martínez LC, Masachessi G, Carruyo G, et al. Picobirnavirus causes persistent infection in pigs. Infection, Genetics and Evol 2010;10(7):984-988.
  16. Legoff J, Resche-Rigon M, Bouquet J, et al. The eukaryotic gut virome in hematopoietic stem cell transplantation: New clues in enteric graft-versus-host disease. Nat Med 2017;23(9):1080-1085.
  17. Takiuchi E, Macedo R, Kunz AF, et al. Electrophoretic RNA genomic profiles of Brazilian Picobirnavirus (PBV) strains and molecular characterization of a PBV isolated from diarrheic calf. Virus Res 2016;211:58-63.
  18. Buzinaro MG, Freitas PPS, Kisiellius JJ, et al. Identification of a bisegmented double-stranded RNA virus (picobirnavirus) in calf faeces. Vet J 2003; 166 (2):185-187.
  19. de Oliveira Navarro J, Candido M, de Almeida-Queiroz SR, et al. Genetic diversity of bovine Picobirnavirus, Brazil. Virus Genes 2018;54(5):724-728.
  20. Laemmli UK. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 1970;227(5259):680-685.
  21. Gray J, Iturriza-Gómara M. Rotaviruses. In: Stephenson J, Warnes A (Eds). Diagnostic virology protocols. Methods in molecular biology (Methods and Protocols), vol 665. Totowa, USA: Humana Press 2010; 325-355.
  22. Kumar S, Stecher G, Li M, et al: MEGA X: Molecular evolutionary genetics analysis across computing platforms. Mol Biol Evol 2018;35(6):1547-1549.
  23. Saitou N, Nei M. The neighbor-joining method: A new method for reconstructing phylogenetic trees. Mol Biol Evol 1987;4(4):406-425.
  24. Chinsangaram J, Akita GY, Osburn BI. Detection of bovine group Brotaviruses in feces by polymerase chain reaction. J Vet Diag Invest 1994;6(3):302-307.
  25. Ganesh B, Nagashima S, Ghosh S, et al. 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;2(1):61-72.
  26. Bányai K, Martella V, Bogdán Á, et al. Genogroup I picobirnaviruses in pigs: evidence for genetic diversity and relatedness to human strains. J Gen Virol 2008;89(Pt 2):534-539.
  27. Collier AM, Lyytinen OL, Guo YR, et al. Initiation of RNA polymerization and polymerase encapsidation by a small dsRNA virus. PLoS Pathog 2016;12(4):e1005523. doi:10.1371/journal.ppat.1005523.
  28. Woo PCY, Teng JLL, Bai R, et al. High diversity of Genogroup I picobirnaviruses in mammals. Front Microbiol. 2016;7:1886. doi: 10.3389/fmicb. 01886.
  29. Woo PCY, Teng JLL, Bai R, et al. Novel picobirnaviruses in respiratory and alimentary tracts of cattle and monkeys with large intra- and inter-host diversity. Viruses. 2019;11(6):574. doi: 10.3390/v11060574.