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Picobirnavirus: A Putative Emerging Threat to Humans and Animals

 

Jobin Jose Kattoor, Shubhankar Sircar, Sharad Saurab, Shanmuganathan Subramaniyan, Kuldeep Dhama, Yashpal Singh Malik*

ICAR-Indian Veterinary Research Institute, Izatnagar 243122, Bareilly, Uttar Pradesh, India.

 

Abstract | Diarrheal diseases remain fatal threat to human and animal population with the emergence of new types of pathogens. Among them, viral gastroenteritis plays a lion share with a number ranging over 100 different types including emerging and re-emerging types of viruses. Recent viral metagenomics studies confirm the co-existence of viruses in gastrointestinal tract of several different host species. A Picobirnavirus, consisting of 2 segments, has recently attained attention due to its wide host range and genetic variability. Until 2011, these small viruses were not considered as a separate virus family, when a new family (Picobirnaviridae) was approved by the International Committee on Taxonomy of Viruses (ICTV). Currently two distinct genogroups (GG-I and GG-II) and one predicted genogroup (GG-III) are included in the Picobirnaviridae family. Recently, picobirnavirus infections have been reported from almost all species including wild animals where persistent infection of the virus is also reported. Picobirnaviruses (PBVs) are also reported as opportunistic pathogens in immuno compromised hosts including HIV infected patients. Presence of atypical picobirnaviruses with shorter genomic segments along with genetic closeness of animal and human PBVs and its ability to infect immuno-compromised hosts pose a heavy threat for all human and animal. Currently RNA dependent RNA polymerase based RT-PCR detection is considered as a rapid and sensitive method for detection of PBV. SYBR based real time PCR, RNA PAGE analysis, electron microscopy also serve as detection methods for PBVs. Unavailability of permissive cell lines or animal models remain hurdles for studying the different molecular mechanisms for viral entry, disease causation or even the mode of persistence in reservoir hosts.

 

Keywords | Picobirnavirus, Enteritis, Genogroups, Diagnosis, Epidemiology

 

Editor | Muhammad Munir, The Pirbright Institute, Pirbright, Woking, UK.

Received | May23, 2016; Accepted | June 12, 2016; Published | June 17, 2016

*Correspondence | Yashpal Singh Malik, ICAR-Indian Veterinary Research Institute, Izatnagar 243122, Bareilly, Uttar Pradesh, India; Email: malikyps@ivri.res.in

Citation | Kattoor JJ, Sircar S, Saurab S, Subramaniyan S, Dhama K, Malik YS (2016). Picobirnavirus: A putative emerging threat to humans and animals. Adv. Anim. Vet. Sci. 4(6): 327-331.

DOI | Http://dx.doi.org/10.14737/journal.aavs/2016/4.6.327.331

ISSN (Online) | 2307-8316; ISSN (Print) | 2309-3331

Copyright © 2016 Kattoor et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

 

Gastrointestinal tract infections are now recognized as crucial health problem and are one of the major challenges to growing livestock sector as well as human population throughout the world (Kosek et al., 2003; Clark and McKendrick, 2004). Amid several causes, enteric viruses inflict greater risk and currently include over 100 viruses, few of which include emerging, re-emerging and novel pathogens, that affect animals and/or humans at various stages of life (Wilhelmi et al., 2003; Oude-Munnink and van dek Hoek, 2016). The faecal virome analysis has been able to reveal several viruses associated with acute gastroenteritis, such as novel enteric coronaviruses, bocavirus, kobuvirus, sapelovirus, salivirus, cosavirus, and others. Along with the other recently recognized viruses, Picobirnavirus (PBV) is highly versatile because of its broad host range and genetic diversity. PBV is inflicting potential jeopardy for a number of host species including humans. PBV has been detected in several animal and environmental samples through various molecular techniques (Ganesh et al., 2014). It is an ultra-small (35 nm in diameter), non-enveloped virus possessing two genomic segments of double-stranded RNA. In its initial period of detection (1988), it was named a ‘Birna-like’ virus under the family Birnaviridae (Pereira et al., 1988a; Pereira et al., 1988b). Upon availability of further sequence details during the next one decade (1990-2000), it was classified as a new family member with approval of International Committee on Taxonomy of Viruses (ICTV) (Delmas, 2011). It exhibits two types of genome profiles (large and small) on RNA-PAGE following silver impregnation, which is based on migration distance and size of its 2 genomic segments. The large genomic profile is characterized by segments with size of 2.7 kbp and 1.9 kbp as compared to the smaller one where segments correspond to 2.2 kbp and 1.2 kbp, respectively (Malik et al., 2014). The capsid protein and the viral RNA-dependent RNA polymerase (RdRp) of PBV is encoded by genomic segment 1 (2.2–2.7 kbp) and 2 (1.2–1.9 kbp), respectively. On the basis of RdRp gene sequence diversity, PBVs are classified into two genogroups, namely genogroup-I and II (Rosen et al., 2000). Besides, a third genogroup has also been reported in humans more recently in 2014 (Smits et al., 2014). Genogrouping based on RdRp gene helps in the identification of specific viral genogroups circulating in animals across the different countries. Despite its evolutionary association with “partitiviruses” especially fungi partitiviruses, the PBV is classified under a new family ‘Picobirnaviridae’ with a single genus, Picobirnavirus. It includes two species namely human Picobirnavirus (type species) and rabbit Picobirnavirus (designated species) (Delmas, 2011).

 

Since its discovery in 1988, PBV has been detected in faecal specimens of numerous domestic and captive animal species such as rats (Pereira et al., 1988b; Fregolente et al., 2009), chickens (Alfieri et al., 1989; Leite et al., 1990; Monteiro et al., 1991; Tamehiro et al., 2003; Fregolente et al., 2009; Ribeiro et al., 2014), hamsters (Pereira et al., 1988b), guinea pigs (Pereira et al., 1989), pigs (Gatti et al., 1989; Chasey et al., 1990; Ludert et al., 1991; Pongsuwanna et al., 1996; Carruyo et al., 2008; Banyai et al., 2008; Martinez et al., 2010; Smits et al., 2011; Ganesh et al., 2012), dogs (Fregolente et al., 2009; Costa et al., 2004), giant anteaters (Haga et al., 1999), equine (Ganesh et al., 2011), foals (Browning et al., 1991), bovine calves (Buzinaro et al., 2003; Ghosh et al., 2009; Malik et al., 2011; Malik et al., 2014; Takiuchi et al., 2016), water buffalo calf (Malik et al., 2013), camels (Woo et al., 2014), snake (Fregolente et al., 2009), and several cat family members. It is noteworthy that PBV is not yet established as an etiological agent of diarrhea in animals (Malik et al., 2014). Although it may not be the primary cause of gastroenteritis and is most often isolated as co-infecting agent with other pathogens known to cause diarrhea such as Rotavirus (Alfieri et al., 1994; Bhattacharya et al., 2006; Bhattacharya et al., 2007; Giordano et al., 2008), Astrovirus (Bhattacharya et al., 2006; Bhattacharya et al., 2007), Caliciviruses (Banyai et al., 2003), Escherichia coli (Barreto et al., 2006), and Salmonella (Bhattacharya et al., 2007) but may have synergistic effect in association with the primary enteric causative agents. Studies on PBV detection conclude that captive animals might be serving as alternative hosts or reservoir, while domestic animals get opportunistic infection of PBVs depending upon different physiological conditions (age, lactation, pregnancy, and stress). Moreover, the PBV infection in asymptomatic carriers is found to be persistent. The virus infects hosts in their early stages (mostly first week) of life followed by establishment of persistent infection in undefined location until the beginning of adulthood as evidenced in an adult orangutan and greater rheas (Masachessi et al., 2015). It is assumed that modulation of the viral and cellular gene expression and/or alteration in the host immune response probably play an important role in the persistence of PBVs. However, our understanding regarding the molecular mechanisms that govern the persistence/asymptomatic coexistence of PBV in captive hosts and the potential host suitability to maintain this relationship is still in its infancy. Unfortunately, the unavailability of recognized permissive cell lines and animal model for PBVs obstructs its isolation and clinico-pathological studies. Further, some unusual PBVs with smaller genome (1.7 and 1.3 kb) have also been detected in the oocysts of Cryptosporidium parvum from human and calves (Ng et al., 2014). Contrary to the typical PBVs, these unusual PBVs exhibit striking differences in coding specificity of genomic segment; as the segment 1 and 2 encodes for RdRp and capsid genes, respectively.

 

Picobirnaviruses are detected using Electron microscopy or molecular techniques like RNA-PAGE (polyacrylamide gel electrophoresis), reverse-transcription - polymerase chain reaction assay (RT-PCR) etc. During the early stages of life, the virus is detectable by RT-PCR only but at later stages; it is also detectable by RNA-PAGE. Epidemiological studies across the world in different animal species deploying various diagnostic techniques indicate presence of PBVs up to 65 % in porcine (Bányai et al., 2008), 3.7 % in bovines (Malik et al., 2011), 14.3 % in equines (Ganesh et al., 2011), 1.8 % in canines (Costa et al., 2004), 49.4 % in chickens (Ribeiro et al., 2014), and 47 % in other animals (Fregolente et al., 2009). The virus is also detected in sewage and surface water with a high frequency potentiating its putative zoonotic potential with emerging and/or re-emerging threat to a number of animals in different geographical locations. Besides the gastrointestinal tract, PBV has also been isolated from the respiratory tract of pigs with no evidence of visible respiratory or other diseases (Smits et al., 2011). Likewise, it has also been identified in immunocompromised patients such as those infected with HIV (Giordano et al. 1998; González et al., 1998). A recent viral metagenomics study from Bangladesh in wild macaques reported around 184 different viruses of animal and human origin, in which 120 (65.21%) were picobirnaviruses (Anthony et. al., 2015). These reports advocate its opportunistic infection together with inhabitant setting and expand our perceptive on the tropism as well as host range of the virus. As of now, we don’t have thorough understanding about the replication strategies adopted by the virus and role of adaptive immunity. Nevertheless, the evolutionary closeness of animal PBVs with human ones and detection of the virus from the sewage depict the potential threat vis-à-vis infection acquirement and cross species transmission.

 

We have been working on PBV since 2008 with successful development of RdRp gene based novel genus specific RT-PCR (Malik et al., 2013) and SYBR Green real-time qPCR assay (Haq et al., 2015). Molecular epidemiological studies carried on several animal host species indicate their relationship with diarrhea as alone or in combination with other enteric pathogens. We have been the first to demonstrate occurrence of PBV genogroup II in bovine species (Malik et al., 2014) and detection of PBV in bubaline species (Malik et al., 2013). Although due exploration of various hidden aspects is needed to better understand this virus and its etiopathology, which would help to devise appropriate control strategies.

 

Conclusions

 

Picobirnaviruses (PBVs) are small bi-segmented dsRNA viruses of 35 nm diameter, which are considered as one among the important gastrointestinal infection causing viruses. In 2011, ICTV classified PBVs into a new family Picobirnaviridae, which were earlier included in Birnaviridae because of its bi-segmented double stranded RNA genome. After its discovery in 1988, it has been documented from different host species including domesticated, wild animals, reptiles, birds and humans. Even though PBVs are not established as a primary etiological agent for diarrhea, their co-existence in enteritis conditions have been reported by several researchers. Till now, two established genogroups (I and II) and one putative genogroups (III) have been identified in picobirnaviruses. Absence of permissive cell lines and specific animal models hinder molecular mechanism studies for PBVs. Recent metagenomic analyses indicate enormous presence of PBV in different host species samples and environmental samples. Persistence of PBV infection as studied in wild animals and its ability to infect immuno-compromised hosts makes PBV to be noted as serious emerging infectious agents. Even though EM, RNA-PAGE, qPCR has been devised for PBV detection, RdRp based RT-PCR is considered as the rapid and sensitive diagnostic method for PBVs.

 

Acknowledgements

 

The authors are thankful for the support of Director, Indian Veterinary Research Institute, Izatnagar, U. P. India for providing facilities to carry out the basis for this work.

 

conflict of interests

 

There is no conflict of interest.

 

authors’ contribution

 

All authors contributed equally.

 

Reference

 

  • Alfieri AA, Alfieri AF, Freitas JC, da Silva CA, Freire RL, Barros AR, Barreiros MAB, Muller EE (1994).Occurrence of Escherichia coli, rotavirus, picobirnavirus and Cryptosporidium parvum in a post weaning diarrhoea focus in swine. Cienc. Agrar. 5(1): 5–7.
  • Alfieri F, Alfieri AA, Resende JS, Resende M (1989). A new bi-segmented double stranded RNA virus in avian feces. Arquivo Brasileiro de Medicina Veterin´aria e Zootecnia. 40: 437–440
  • Anthony SJ, Islam A, Johnson C, Navarrete-Macias I, Liang E, Jain K, Hitchens PL, Che X, Soloyvov A, Hicks AL, Ojeda-Flores R,Zambrana-Torrelio C, Ulrich W, Rostal MK, Petrosov A, Garcia J, Haider N, Wolfe N, Goldstein T, Morse SS, Rahman M, Epstein JH, Mazet JK, Daszak P, Lipkin WI (2015). Non-random patterns in viral diversity. Nat. Commun. 22(6): 8147. http://dx.doi.org/10.1038/ncomms9147
  • Bányai K, Martella V, Bogdán A, Forgách P, Jakab F, Meleg E, Bíró H, Melegh B, Szucs G (2008). Genogroup I picobirnaviruses in pigs: evidence for genetic diversity and relatedness to human strains. J. Gen. Virol. 89(2): 534–539. http://dx.doi.org/10.1099/vir.0.83134-0
  • Bányai K, Jakab F, Reuter G, Bene J, Uj M, Melegh B, Szücs G (2003). Sequence heterogeneity among human picobirnaviruses detected in a gastroenteritis outbreak. Arch. Virol. 148 (12): 2281–2291. http://dx.doi.org/10.1007/s00705-003-0200-z
  • Barreto ML, Milroy CA, Strina A, Prado MS, Leite JP, Ramos EA, Ribeiro H, Alcântara-Neves NM, Teixeira Mda G, Rodrigues LC, Ruf H, Guerreiro H,Trabulsi LR (2006). Community-based monitoring of diarrhea in urban Brazilian children: Incidence and associated pathogens. Trans. R. Soc. Trop. Med. Hyg. 100 (3): 234–242. http://dx.doi.org/10.1016/j.trstmh.2005.03.010
  • Bhattacharya R, Sahoo GC, Nayak MK, Ghosh S, Dutta P, Bhattacharya MK, Mitra U, Gangopadhyay D, Dutta S, Niyogi SK, Saha DR, Naik TN,Bhattacharya SK, Krishnan T (2006). Molecular epidemiology of human astrovirus infections in Kolkata, India. Infect. Genet. Evol. 6(6): 425–435. http://dx.doi.org/10.1016/j.meegid.2006.02.005
  • Bhattacharya R Sahoo GC, Nayak MK, Rajendran K, Dutta P, Mitra U, Bhattacharya MK, Naik TN, Bhattacharya SK, Krishnan T (2007). Detection of Geno-group I and II human picobirnaviruses showing small genomic RNA profile causing acute watery diarrhoea among children in Kolkata, India. Infect. Genet. Evol. 7(2): 229–238. http://dx.doi.org/10.1016/j.meegid.2006.09.005
  • Browning GF, Chalmers RM, Snodgrass DR, Batt RM, Hart CA, Ormarod SE, Leadon D, Stoneham SJ, Rossdale PD (1991). The prevalence of enteric pathogens in diarrhoeic thoroughbred foals in Britain and Ireland. Equine Vet. J. 23(6): 405–409. http://dx.doi.org/10.1111/j.2042-3306.1991.tb03751.x
  • Buzinaro MG, Freitas PPS, Kisiellius JJ, Ueda M, Jerez JA (2003). Identification of a bisegmented double-stranded RNA virus (picobirnavirus) in calf faeces. Vet. J. 166 (2):185–187. http://dx.doi.org/10.1016/S1090-0233(03)00031-5
  • Carruyo GM, Mateu G, Martinez LC, Pujo FH, Nates SV, Liprandi F, Ludert JE (2008). Molecular characterization of porcine picobirnaviruses and development of a specific reverse transcription-PCR assay. J. Clin. Microbiol. 46(7): 2402–2405. http://dx.doi.org/10.1128/JCM.00655-08
  • Chasey D (1990). Porcine picobirnavirus in UK. Vet. Rec. 126(18): 465.
  • Clark B, McKendrick M (2004). A review of viral gastroenteritis. Curr. Opin. Infect. Dis. 17(5): 461-9. http://dx.doi.org/10.1097/00001432-200410000-00011
  • Costa AP, Cubel Garcia RCN, Labarthe NV, Leite JPG (2004). Detection of double-stranded RNA viruses in fecal samples of dogs with gastroenteritis in Rio de Janeiro, Brazil,” Arq. Bras. Med. Vet. Zootec. 56(4): 554–557. http://dx.doi.org/10.1590/S0102-09352004000400020
  • Delmas B (2011). Picobirnaviridae. In: King A, Adams M, Carstens E, Lefkowitz E, editors. Virus taxonomy: classification and nomenclature of viruses: ninth report of the International Committee on Taxonomy of Viruses. 1st ed. San Diego: Elsevier. Pp. 535–539.
  • Fregolente MC, de Castro-Dias E, Martins SS, Spilki FR, Allegretti SM, Gatti MS (2009). Molecular characterization of picobirnaviruses from new hosts. Virus Res. 143(1): 134–136. http://dx.doi.org/10.1016/j.virusres.2009.03.006
  • Ganesh B, Banyai K, Kanungo S, Sur D, Malik YS, Kobayashi N (2012). Detection and molecular characterization of porcine picobirnavirus in feces of domestic pigs from Kolkata, India. Indian J. Virol. 23(3): 387–391. http://dx.doi.org/10.1007/s13337-012-0106-z
  • Ganesh B, Banyai K, Masachessi G, Mladenova Z, Nagashima S, Ghosh S, Nataraju SM, Pativada M, Kumar R, Kobayashi N (2011). Geno-group I picobirnavirus in diarrhoeic foals: can the horse serve as a natural reservoir for human infection? Vet. Res. 42(1): 52. http://dx.doi.org/10.1186/1297-9716-42-52
  • Ganesh B, Masachessi G, Mladenova Z (2014). Animal picobirnavirus. Virus Dis. 25: 223–238. http://dx.doi.org/10.1007/s13337-014-0207-y
  • Gatti MS, de Castro AF, Ferraz MM, Fialho AM, Pereira HG (1989). Viruses with bisegmented double-stranded RNA in pig faeces. Res. Vet. Sci. 47(3): 397– 398.
  • Ghosh S, Kobayashi N, Nagashima S, Naik TN (2009). Molecular characterization of full-length genomic segment 2 of a bovine picobirnavirus (PBV) strain: evidence for high genetic diversity with genogroups I PBVs. J. Gen. Virol. 90(10): 2519–2524. http://dx.doi.org/10.1099/vir.0.013987-0
  • Giordano MO, Martinez LC, Rinaldi D, Gúinard S, Naretto E, Casero R, Yacci MR, Depetris AR, Medeot SI, Nates SV (1998). Detection of picobirnavirus in HIV-infected patients with diarrhea in Argentina. J. Acquir. Immune. Defic. Syndr. Hum. Retrovirol. 18: 380–383. http://dx.doi.org/10.1097/00042560-199808010-00010
  • Giordano MO, Masachessi G, Martinez LC, Barril PA, Ferreyra LJ, Isa MB, Nates SV (2008). Two instances of large genome profile picobirnavirus occurrence in Argentinian infants with diarrhea over a 26-year period (1977– 2002). J. Infect. 56(5): 371–375. http://dx.doi.org/10.1016/j.jinf.2008.02.017
  • González GG, Pujol FH, Liprandi F, Deibis L, Ludert JE (1988). Prevalence of enteric viruses in human immunodeficiency virus seropositive patients in Venezuela. J. Med. Virol. 55: 288–292. http://dx.doi.org/10.1002/(SICI)1096-9071(199808)55:4<288::AID-JMV6>3.0.CO;2-X
  • Haga IR, Martins SS, Hosomi ST, Vicentini F, Tanaka H, Gatti MSV (1999). Identification of a bisegmented double-stranded RNAVirus (Picobirnavirus) in Faeces of Giant Anteaters (Myrmecophaga tridactyla). Vet. J. 158(3): 234–236. http://dx.doi.org/10.1053/tvjl.1999.0369
  • Haq AA, Sharma K, Malik YS, Dhama K, Gupta PK (2015). Development of Real-time PCR Assay for Detection of Rotavirus Infection in Diarrheic Bovine Calves. Adv. Anim. Vet. Sci. 3(6): 321-324. http://dx.doi.org/10.14737/journal.aavs/2015/3.6.321-324
  • Kosek M, Bern C, Guerrant RL (2003). The global burden of diarrhoeal disease, as estimated from studies published between 1992 and 2000. Bull. World Health Organ. 81: 197–204.
  • Leite JPG, Monteiro SP, Fialho AM, Pereira HG (1990). A novel avian virus with trisegmented double-stranded RNA and further observations on previously described similar viruses with bisegmented genome. Virus Res. 16(2): 119–126. http://dx.doi.org/10.1016/0168-1702(90)90016-5
  • Ludert JE, Hidalgo M, Gil F,Liprandi F (1991). Identification in porcine faeces of a novel virus with a bisegmented double stranded RNA genome. Arch. Virol. 117(1-2): 97–107. http://dx.doi.org/10.1007/BF01310495
  • Malik YS, Chandrashekar KM, Sharma K, Haq AA, Vaid N, Chakravarti S, Batra M, Singh R, Pandey AB (2011). Picobirnavirus detection in bovine and buffalo calves from foothills of Himalaya and Central India. Trop. Anim. Health. Prod. 43(8): 1475–1478. http://dx.doi.org/10.1007/s11250-011-9834-0
  • Malik YS, Kumar N, Sharma K, Dhama K, Shabbir MZ, Ganesh B, Kobayashi N, Banyai K (2014). Epidemiology, Phylogeny, and Evolution of Emerging Enteric Picobirnaviruses of Animal Origin and Their Relationship to Human Strains. Biomed Res. Int. 2014: 1-13. http://dx.doi.org/10.1155/2014/780752
  • Malik YS, Kumar N, Sharma K, Sharma AK, Sircar S, Jeena LM, Singh NK, Mondal A, Joardar SN, Ganesh B (2013). Molecular characterization of a genetically diverse bubaline picobirnavirus strain, India. Thai J. Vet. Med. 43(4): 609–613.
  • Malik YS, Sharma AK, Kumar N, Sharma K, Ganesh B, Kobayashi N (2014). Identification and characterisation of a novel genogroup II picobirnavirus in a calf in India. Vet. Rec. 174(11): 278. http://dx.doi.org/10.1136/vr.102065
  • Martinez LC, Masachessi G, Carruyo G, Ferreyra LJ, Barrila PA, Isa MB, Giordano MO, Ludert JE, Nates SV (2010). Picobirnavirus causes persistent infection in pigs. Infect. Genet. Evol. 10(7): 984–988. http://dx.doi.org/10.1016/j.meegid.2010.06.004
  • Masachessi G, Ganesh B, Martinez LC, Giordano MO, Barril PA, Isa MB, Pavan GV, Mateos CA, Nates SV (2015). 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. 29:196-202. http://dx.doi.org/10.1016/j.meegid.2014.11.019
  • Monteiro SP, Pereira HG, Fialho AM, Leite JPG (1991). Viruses with segmented double-stranded RNA in chickens. Arquivo Brasileiro de Medicina Veterin´aria e Zootecnia. 42:141–146.
  • Ng TFF, Vega E, Kondov NO, Markey C, Deng X, Gregoricus N, Vinjé J, Delwart E (2014). Divergent Picobirnaviruses in Human Feces. Genome Announc. 2(3): e00415-14. http://dx.doi.org/10.1128/genomeA.00415-14
  • Oude Munnink BB, van der Hoek L (2016). Viruses Causing Gastroenteritis: The Known, The New and Those Beyond. Viruses. 8(2): 42. http://dx.doi.org/10.3390/v8020042
  • Pereira HG, de Araujo HP, Fialho AM, de Castro L, Monteiro SP (1989). A virus with bi-segmented double-stranded RNA genome in guinea pig intestines. Mem´orias do Instituto Oswaldo Cruz. 84(1): 137–140. http://dx.doi.org/10.1590/S0074-02761989000100025
  • Pereira HG, Fialho AM, Flewett TH, Teixeira JMS, Andrade ZP (1988). Novel viruses in human faeces. Lancet. 332(8602): 103–104. http://dx.doi.org/10.1016/S0140-6736(88)90032-3
  • Pereira HG, Flewett TH, Candeias JAN, Barth OM (1988). A virus with a bisegmented double-stranded RNA genome in rat (Oryzomys nigripes) intestines. J. Gen. Virol. 69(11): 2749–2754. http://dx.doi.org/10.1099/0022-1317-69-11-2749
  • Pongsuwanna Y, Taniguchi K, Chiwakul M, Urasawa T,Wakasugi F,Jayavasuand C, Urasawa S (1996). Serological and genomic characterization of porcine rotaviruses in Thailand: detection of a G10 porcine rotavirus. J. Clin. Microbiol. 34(5): 1050–1057.
  • Ribeiro SR, Bezerra DAM, Kaiano JHL, Oliveira DS, Silvestre RVD, Gabbay YB, Ganesh B, Mascarenhas JDP (2014). Genogroup I avian picobirnavirus detected in Brazilian broiler chickens: a molecular epidemiology study. J. Gen. Virol. 95(1): 117–122. http://dx.doi.org/10.1099/vir.0.054783-0
  • Rosen BI, Fang ZY, Glass RI, Monroe SS (2000). Cloning of human picobirnavirus genomic segments and development of an RT-PCR detection assay. Virol. 277(2): 316– 329. http://dx.doi.org/10.1006/viro.2000.0594
  • Smits SL, Poon LLM, Van leeuwen M, Lau PN, Perera HKK, Malik Peiris JS, Simon JH, Osterhaus DME (2011). Genogroup I and II picobirnaviruses in respiratory tracts of pigs. Emerg. Infect. Dis. 17(12): 2328–2330. http://dx.doi.org/10.3201/eid1712.110934
  • Smits SL, Schapendonk CM, van Beek J, Vennema H, Schürch AC, Schipper D, Bodewes R, Haagmans BL, Osterhaus AD, Koopmans MP (2014). New Viruses in Idiopathic Human Diarrhea Cases, The Netherlands. Emerg. Infect. Dis. 20(7): 1218-22. http://dx.doi.org/10.3201/eid2007.140190
  • Takiuchi E, Macedo R, Kunz AF, Gallego JC, de Mello JL, Otonel RA, Alfieri AA (2016). Electrophoretic RNA genomic profiles of Brazilian Picobirnavirus (PBV) strains and molecular characterization of a PBV isolated from diarrheic calf. Virus Res. 211: 58-63. http://dx.doi.org/10.1016/j.virusres.2015.09.022
  • Tamehiro CY, Alfieri AF, M´edici KC, Alfieri AA (2003). Segmented double-stranded genomic RNA viruses in fecal samples from broiler chicken, Braz. J. Microbiol. 34(4): 349–353. http://dx.doi.org/10.1590/S1517-83822003000400013
  • Wilhelmi I, Roman E, Sánchez-Fauquier A (2003). Viruses causing gastroenteritis. Clin. Microbiol. Infect. 9: 247-262. http://dx.doi.org/10.1046/j.1469-0691.2003.00560.x
  • Woo PC, Lau SK, Teng JL, Tsang AK, Joseph M, Wong EY, Tang Y, Sivakumar S, Bai R, Wernery R, Wernery U, Yuen KY (2014). Metagenomic analysis of viromes of dromedary camel fecal samples reveals large number and high diversity of circoviruses and picobirnaviruses. .Virol. 471: 117-125. http://dx.doi.org/10.1016/j.virol.2014.09.020
  •