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 inJournal of Veterinary Medical Science Vol. 86; no. 9; pp. 986 - 991
Main Authors Shwe Thiri MAUNG MAUNG KHIN, SHEIKHI, Mohammad Jafar, TAKEMAE, Hitoshi, MIZUTANI, Tetsuya, FURUYA, Tetsuya
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LanguageEnglish
Published Japan 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.
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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10.3390/ani12233375
10.1038/nature06536
10.1038/s41467-024-46151-9
10.1007/s00705-014-2304-z
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animal shelter
picorna-like virus
next-generation sequencing
fesavirus 4
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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.
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12
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3
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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.
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  doi: 10.1099/jgv.0.000279
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  doi: 10.1038/nrmicro2030
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  doi: 10.1007/s13337-014-0207-y
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  doi: 10.1128/JVI.05217-11
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  doi: 10.1099/vir.0.043182-0
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  doi: 10.1128/JVI.00601-10
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  doi: 10.1016/j.jbiotec.2016.12.022
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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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