First report of fesavirus 4 detection from cats in Japan
Fesaviruses, picorna-like RNA viruses, were discovered in 2014 in feces from cats in an animal shelter in the United States but have not since been reported elsewhere. In this study, we collected cat fecal samples from 20 adult cats from an animal shelter in Tokyo, Japan, and examined them for viral...
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Published in | Journal of Veterinary Medical Science Vol. 86; no. 9; pp. 986 - 991 |
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JAPANESE SOCIETY OF VETERINARY SCIENCE
2024
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Abstract | Fesaviruses, picorna-like RNA viruses, were discovered in 2014 in feces from cats in an animal shelter in the United States but have not since been reported elsewhere. In this study, we collected cat fecal samples from 20 adult cats from an animal shelter in Tokyo, Japan, and examined them for viral pathogens. Next generation sequencing (NGS) was performed to detect both RNA and DNA virus sequences. Sequences of a total of 7 RNA viruses including some common feline pathogenic viruses were detected across 8 samples, while no DNA virus sequences were identified in any sample. Of the RNA virus sequences detected in the samples, two sequences, 4,746 and 4,439 bp, demonstrated 90.3% and 85.0% similarity, respectively, to the fesavirus 4 sequence in the database. To confirm the NGS results, quantitative RT-PCR (qRT-PCR) assays were developed using specific primers and probes designed based on the contig sequences. Based on the qRT-PCR assays, we detected relatively high copy-numbers of fesavirus 4 RNA in the two fecal samples from which the fesavirus 4 sequences were originally obtained, and low copy numbers in other samples. These results demonstrate the presence of fesavirus 4 in cats in Japan for the first time. |
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AbstractList | Fesaviruses, picorna-like RNA viruses, were discovered in 2014 in feces from cats in an animal shelter in the United States but have not since been reported elsewhere. In this study, we collected cat fecal samples from 20 adult cats from an animal shelter in Tokyo, Japan, and examined them for viral pathogens. Next generation sequencing (NGS) was performed to detect both RNA and DNA virus sequences. Sequences of a total of 7 RNA viruses including some common feline pathogenic viruses were detected across 8 samples, while no DNA virus sequences were identified in any sample. Of the RNA virus sequences detected in the samples, two sequences, 4,746 and 4,439 bp, demonstrated 90.3% and 85.0% similarity, respectively, to the fesavirus 4 sequence in the database. To confirm the NGS results, quantitative RT-PCR (qRT-PCR) assays were developed using specific primers and probes designed based on the contig sequences. Based on the qRT-PCR assays, we detected relatively high copy-numbers of fesavirus 4 RNA in the two fecal samples from which the fesavirus 4 sequences were originally obtained, and low copy numbers in other samples. These results demonstrate the presence of fesavirus 4 in cats in Japan for the first time. Fesaviruses, picorna-like RNA viruses, were discovered in 2014 in feces from cats in an animal shelter in the United States but have not since been reported elsewhere. In this study, we collected cat fecal samples from 20 adult cats from an animal shelter in Tokyo, Japan, and examined them for viral pathogens. Next generation sequencing (NGS) was performed to detect both RNA and DNA virus sequences. Sequences of a total of 7 RNA viruses including some common feline pathogenic viruses were detected across 8 samples, while no DNA virus sequences were identified in any sample. Of the RNA virus sequences detected in the samples, two sequences, 4,746 and 4,439 bp, demonstrated 90.3% and 85.0% similarity, respectively, to the fesavirus 4 sequence in the database. To confirm the NGS results, quantitative RT-PCR (qRT-PCR) assays were developed using specific primers and probes designed based on the contig sequences. Based on the qRT-PCR assays, we detected relatively high copy-numbers of fesavirus 4 RNA in the two fecal samples from which the fesavirus 4 sequences were originally obtained, and low copy numbers in other samples. These results demonstrate the presence of fesavirus 4 in cats in Japan for the first time.Fesaviruses, picorna-like RNA viruses, were discovered in 2014 in feces from cats in an animal shelter in the United States but have not since been reported elsewhere. In this study, we collected cat fecal samples from 20 adult cats from an animal shelter in Tokyo, Japan, and examined them for viral pathogens. Next generation sequencing (NGS) was performed to detect both RNA and DNA virus sequences. Sequences of a total of 7 RNA viruses including some common feline pathogenic viruses were detected across 8 samples, while no DNA virus sequences were identified in any sample. Of the RNA virus sequences detected in the samples, two sequences, 4,746 and 4,439 bp, demonstrated 90.3% and 85.0% similarity, respectively, to the fesavirus 4 sequence in the database. To confirm the NGS results, quantitative RT-PCR (qRT-PCR) assays were developed using specific primers and probes designed based on the contig sequences. Based on the qRT-PCR assays, we detected relatively high copy-numbers of fesavirus 4 RNA in the two fecal samples from which the fesavirus 4 sequences were originally obtained, and low copy numbers in other samples. These results demonstrate the presence of fesavirus 4 in cats in Japan for the first time. Fesaviruses, picorna-like RNA viruses, were discovered in 2014 in feces from cats in an animal shelter in the United States but have not since been reported elsewhere. In this study, we collected cat fecal samples from 20 adult cats from an animal shelter in Tokyo, Japan, and examined them for viral pathogens. Next generation sequencing (NGS) was performed to detect both RNA and DNA virus sequences. Sequences of a total of 7 RNA viruses including some common feline pathogenic viruses were detected across 8 samples, while no DNA virus sequences were identified in any sample. Of the RNA virus sequences detected in the samples, two sequences, 4,746 and 4,439 bp, demonstrated 90.3% and 85.0% similarity, respectively, to the fesavirus 4 sequence in the database. To confirm the NGS results, quantitative RT-PCR (qRT-PCR) assays were developed using specific primers and probes designed based on the contig sequences. Based on the qRT-PCR assays, we detected relatively high copy-numbers of fesavirus 4 RNA in the two fecal samples from which the fesavirus 4 sequences were originally obtained, and low copy numbers in other samples. These results demonstrate the presence of fesavirus 4 in cats in Japan for the first time. |
ArticleNumber | 24-0243 |
Author | Shwe Thiri MAUNG MAUNG KHIN FURUYA, Tetsuya TAKEMAE, Hitoshi MIZUTANI, Tetsuya SHEIKHI, Mohammad Jafar |
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Cites_doi | 10.1177/0300985813511129 10.1111/mam.12332 10.1099/vir.0.069674-0 10.1099/jgv.0.000279 10.1038/nrmicro2030 10.1007/s13337-014-0207-y 10.1128/JVI.05217-11 10.1099/vir.0.043182-0 10.1128/JVI.00601-10 10.1016/j.jbiotec.2016.12.022 10.3390/ani12233375 10.1038/nature06536 10.1038/s41467-024-46151-9 10.1007/s00705-014-2304-z |
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References | 11. Reuter G, Pankovics P, Delwart E, Boros Á. 2015. A novel posavirus-related single-stranded RNA virus from fish (Cyprinus carpio). Arch Virol 160: 565–568. 14. Zhang W, Li L, Deng X, Kapusinszky B, Pesavento PA, Delwart E. 2014. Faecal virome of cats in an animal shelter. J Gen Virol 95: 2553–2564. 2. Forcina G, Pérez-Pardal L, Carvalheira J, Beja-Pereira A. 2022. Gut microbiome studies in livestock: achievements, challenges, and perspectives. Animals (Basel) 12: 3375. 8. Pesavento PA, Murphy BG. 2014. Common and emerging infectious diseases in the animal shelter. Vet Pathol 51: 478–491. 6. Koonin EV, Wolf YI, Nagasaki K, Dolja VV. 2008. The Big Bang of picorna-like virus evolution antedates the radiation of eukaryotic supergroups. Nat Rev Microbiol 6: 925–939. 5. Kapoor A, Simmonds P, Lipkin WI, Zaidi S, Delwart E. 2010. Use of nucleotide composition analysis to infer hosts for three novel picorna-like viruses. J Virol 84: 10322–10328. 4. Jones KE, Patel NG, Levy MA, Storeygard A, Balk D, Gittleman JL, Daszak P. 2008. Global trends in emerging infectious diseases. Nature 451: 990–993. 1. Deurenberg RH, Bathoorn E, Chlebowicz MA, Couto N, Ferdous M, García-Cobos S, Kooistra-Smid AM, Raangs EC, Rosema S, Veloo AC, Zhou K, Friedrich AW, Rossen JW. 2017. Application of next generation sequencing in clinical microbiology and infection prevention. J Biotechnol 243: 16–24. 7. Oude Munnink BB, Cotten M, Deijs M, Jebbink MF, Bakker M, Jazaeri Farsani SM, Canuti M, Kellam P, van der Hoek L. 2015. A novel genus in the order Picornavirales detected in human stool. J Gen Virol 96: 3440–3443. 13. Szentivanyi T, Oedin M, Rocha R. 2023. Cat-wildlife interactions and zoonotic disease risk: a call for more and better community science data. Mammal Rev 54: 93–104. 10. Radford AD, Chapman D, Dixon L, Chantrey J, Darby AC, Hall N. 2012. Application of next-generation sequencing technologies in virology. J Gen Virol 93: 1853–1868. 3. Ganesh B, Masachessi G, Mladenova Z. 2014. Animal picobirnavirus. Virusdisease 25: 223–238. 9. Plowright RK, Ahmed AN, Coulson T, Crowther TW, Ejotre I, Faust CL, Frick WF, Hudson PJ, Kingston T, Nameer PO, O’Mara MT, Peel AJ, Possingham H, Razgour O, Reeder DM, Ruiz-Aravena M, Simmons NB, Srinivas PN, Tabor GM, Tanshi I, Thompson IG, Vanak AT, Vora NM, Willison CE, Keeley ATH. 2024. Ecological countermeasures to prevent pathogen spillover and subsequent pandemics. Nat Commun 15: 2577. 12. Shan T, Li L, Simmonds P, Wang C, Moeser A, Delwart E. 2011. The fecal virome of pigs on a high-density farm. J Virol 85: 11697–11708. 11 12 13 14 1 2 3 4 5 6 7 8 9 10 |
References_xml | – reference: 8. Pesavento PA, Murphy BG. 2014. Common and emerging infectious diseases in the animal shelter. Vet Pathol 51: 478–491. – reference: 13. Szentivanyi T, Oedin M, Rocha R. 2023. Cat-wildlife interactions and zoonotic disease risk: a call for more and better community science data. Mammal Rev 54: 93–104. – reference: 3. Ganesh B, Masachessi G, Mladenova Z. 2014. Animal picobirnavirus. Virusdisease 25: 223–238. – reference: 5. Kapoor A, Simmonds P, Lipkin WI, Zaidi S, Delwart E. 2010. Use of nucleotide composition analysis to infer hosts for three novel picorna-like viruses. J Virol 84: 10322–10328. – reference: 6. Koonin EV, Wolf YI, Nagasaki K, Dolja VV. 2008. The Big Bang of picorna-like virus evolution antedates the radiation of eukaryotic supergroups. Nat Rev Microbiol 6: 925–939. – reference: 1. Deurenberg RH, Bathoorn E, Chlebowicz MA, Couto N, Ferdous M, García-Cobos S, Kooistra-Smid AM, Raangs EC, Rosema S, Veloo AC, Zhou K, Friedrich AW, Rossen JW. 2017. Application of next generation sequencing in clinical microbiology and infection prevention. J Biotechnol 243: 16–24. – reference: 7. Oude Munnink BB, Cotten M, Deijs M, Jebbink MF, Bakker M, Jazaeri Farsani SM, Canuti M, Kellam P, van der Hoek L. 2015. A novel genus in the order Picornavirales detected in human stool. J Gen Virol 96: 3440–3443. – reference: 9. Plowright RK, Ahmed AN, Coulson T, Crowther TW, Ejotre I, Faust CL, Frick WF, Hudson PJ, Kingston T, Nameer PO, O’Mara MT, Peel AJ, Possingham H, Razgour O, Reeder DM, Ruiz-Aravena M, Simmons NB, Srinivas PN, Tabor GM, Tanshi I, Thompson IG, Vanak AT, Vora NM, Willison CE, Keeley ATH. 2024. Ecological countermeasures to prevent pathogen spillover and subsequent pandemics. Nat Commun 15: 2577. – reference: 10. Radford AD, Chapman D, Dixon L, Chantrey J, Darby AC, Hall N. 2012. Application of next-generation sequencing technologies in virology. J Gen Virol 93: 1853–1868. – reference: 12. Shan T, Li L, Simmonds P, Wang C, Moeser A, Delwart E. 2011. The fecal virome of pigs on a high-density farm. J Virol 85: 11697–11708. – reference: 4. Jones KE, Patel NG, Levy MA, Storeygard A, Balk D, Gittleman JL, Daszak P. 2008. Global trends in emerging infectious diseases. Nature 451: 990–993. – reference: 11. Reuter G, Pankovics P, Delwart E, Boros Á. 2015. A novel posavirus-related single-stranded RNA virus from fish (Cyprinus carpio). Arch Virol 160: 565–568. – reference: 2. Forcina G, Pérez-Pardal L, Carvalheira J, Beja-Pereira A. 2022. Gut microbiome studies in livestock: achievements, challenges, and perspectives. Animals (Basel) 12: 3375. – reference: 14. Zhang W, Li L, Deng X, Kapusinszky B, Pesavento PA, Delwart E. 2014. Faecal virome of cats in an animal shelter. J Gen Virol 95: 2553–2564. – ident: 8 doi: 10.1177/0300985813511129 – ident: 13 doi: 10.1111/mam.12332 – ident: 14 doi: 10.1099/vir.0.069674-0 – ident: 7 doi: 10.1099/jgv.0.000279 – ident: 6 doi: 10.1038/nrmicro2030 – ident: 3 doi: 10.1007/s13337-014-0207-y – ident: 12 doi: 10.1128/JVI.05217-11 – ident: 10 doi: 10.1099/vir.0.043182-0 – ident: 5 doi: 10.1128/JVI.00601-10 – ident: 1 doi: 10.1016/j.jbiotec.2016.12.022 – ident: 2 doi: 10.3390/ani12233375 – ident: 4 doi: 10.1038/nature06536 – ident: 9 doi: 10.1038/s41467-024-46151-9 – ident: 11 doi: 10.1007/s00705-014-2304-z |
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Snippet | Fesaviruses, picorna-like RNA viruses, were discovered in 2014 in feces from cats in an animal shelter in the United States but have not since been reported... |
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SubjectTerms | animal shelter Animal shelters Animals Cat Diseases - diagnosis Cat Diseases - virology cat feces sample Cats DNA probes DNA sequencing DNA viruses Feces Feces - virology Female fesavirus 4 High-Throughput Nucleotide Sequencing - veterinary Japan - epidemiology Male Next-generation sequencing Nucleotide sequence picorna-like virus Picornaviridae - classification Picornaviridae - genetics Picornaviridae - isolation & purification Picornaviridae Infections - diagnosis Picornaviridae Infections - epidemiology Picornaviridae Infections - veterinary Picornaviridae Infections - virology Polymerase chain reaction RNA viruses RNA, Viral - genetics Shelters Virology Viruses |
Title | First report of fesavirus 4 detection from cats in Japan |
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