TY - JOUR
T1 - Rotavirus incapable of NSP6 expression can cause diarrhea in suckling mice
AU - Fukuda, Saori
AU - Kugita, Masanori
AU - Higashimoto, Yuki
AU - Shiogama, Kazuya
AU - Tsujikawa, Hanako
AU - Moriguchi, Kyoko
AU - Ito, Naoto
AU - Sugiyama, Makoto
AU - Nagao, Shizuko
AU - Murata, Takayuki
AU - Taniguchi, Koki
AU - Komoto, Satoshi
N1 - Funding Information:
This study was supported in part by The Research Program on Emerging and Re-emerging Infectious Diseases of the Japan Agency for Medical Research and Development, AMED (18fk0108018h0403, 18fk0108034h1102, 19fk0108034h1103, 20fk0108121h0601, and 21fk0108121h0602 to S.K.), JSPS KAKENHI (18K07150 and 21K07057 to S.K., and 21K08498 to S.F.), The Mochida Memorial Foundation for Medical and Pharmaceutical Research (S.K.), and The Takeda Science Foundation (S.K.). We are grateful to the Fourth Laboratory of the Department of Pathology of Keio University School of Medicine, and the Centre for Joint Research Facilities Support in Fujita Health University for the technical assistance.
Funding Information:
This study was supported in part by the Research Program on Emerging and Re-emerging Infectious Diseases of the Japan Agency for Medical Research and Development, AMED (18fk0108018h0403, 18fk0108034h1102, 19fk0108034h1103, 20fk0108121h0601, and 21fk0108121h0602 to S.K.), JSPS KAKENHI (18K07150 and 21K07057 to S.K., and 21K08498 to S.F.), the Mochida Memorial Foundation for Medical and Pharmaceutical Research (S.K.), and the Takeda Science Foundation (S.K.).
Publisher Copyright:
© 2022 The Authors.
PY - 2022
Y1 - 2022
N2 - The group A rotavirus (RVA) genome comprising 11 double-stranded RNAs encodes six structural proteins (VP1-VP4, VP6, and VP7) and six non-structural proteins (NSP1-NSP6). Among these 12 rotaviral proteins, NSP6 has been less studied as to its function. We previously prepared a recombinant NSP6-deficient RVA derived from simian strain SA11-L2 by reverse genetics, and found that the NSP6-deficient virus grew well in cell culture, although its growth was less abundant than that of the parental SA11-L2 strain. In this study, we examined the potency of a recombinant RVA incapable of NSP6 expression to cause diarrhoea in suckling mice. The suckling mice infected with the NSP6-deficient virus apparently experienced diarrhoea, although the symptom was milder and the duration of diarrhoea was shorter than in the mice infected with the authentic SA11-L2 strain. Thus, together with the results obtained for cultured cells in the previous study, it can be concluded that NSP6 is not necessarily required for replication and pathogenicity in vitro and in vivo.
AB - The group A rotavirus (RVA) genome comprising 11 double-stranded RNAs encodes six structural proteins (VP1-VP4, VP6, and VP7) and six non-structural proteins (NSP1-NSP6). Among these 12 rotaviral proteins, NSP6 has been less studied as to its function. We previously prepared a recombinant NSP6-deficient RVA derived from simian strain SA11-L2 by reverse genetics, and found that the NSP6-deficient virus grew well in cell culture, although its growth was less abundant than that of the parental SA11-L2 strain. In this study, we examined the potency of a recombinant RVA incapable of NSP6 expression to cause diarrhoea in suckling mice. The suckling mice infected with the NSP6-deficient virus apparently experienced diarrhoea, although the symptom was milder and the duration of diarrhoea was shorter than in the mice infected with the authentic SA11-L2 strain. Thus, together with the results obtained for cultured cells in the previous study, it can be concluded that NSP6 is not necessarily required for replication and pathogenicity in vitro and in vivo.
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U2 - 10.1099/jgv.0.001745
DO - 10.1099/jgv.0.001745
M3 - Article
C2 - 35639587
AN - SCOPUS:85131156386
SN - 0022-1317
VL - 103
JO - Journal of General Virology
JF - Journal of General Virology
IS - 5
M1 - 001745
ER -