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Complete genotyping of unusual species A rotavirus G12P[11] and G10P[14] isolates and evidence of frequent in vivo reassortment among the rotaviruses detected in children with diarrhea in Kolkata, India, during 2014.

Authors :
Mandal, Paulami
Mullick, Satarupa
Nayak, Mukti
Mukherjee, Anupam
Ganguly, Nupur
Niyogi, Prabal
Panda, Samiran
Chawla-Sarkar, Mamta
Source :
Archives of Virology. Oct2016, Vol. 161 Issue 10, p2773-2785. 13p.
Publication Year :
2016

Abstract

Species A rotaviruses (RVA) are the most important cause of acute gastroenteritis in the young of humans and many animal species globally. G1P[8], G2P[4], G3P[8], G4P[8], G9P[6/8] and G12P[6/8] are the predominantly isolated genotypes throughout the world including India. Unusual genotypes from different host species such as G5, G6, G8, G10 and G11 have also been reported in humans with low frequency. In the present study, among >650 RVA positive stool samples collected from children with diarrhea in Kolkata, India, during 2014, two isolates each of the genotype G12P[11] and G10P[14] were obtained and their genomes completely sequenced. The full genotype constellations were G12-P[11]-I1-R1-C1-M2-A1-N1-T2-E1-H1 and G12-P[11]-I1-R1-C1-M1-A5-N1-T1-E1-H1 for G12P[11] viruses, suggesting several reassortments between Wa- and DS-1-like human RVA strains, including possible reassortment of a simian NSP1 gene. The G10P[14] viruses (G10-P[14]-I2-R2-C2-M2-A11-N2-T6-E2-H3) were found to contain multiple genes closely related to RVAs of artiodactyl origin, highlighting the role of inter-host species transmissions of RVAs. From the G/P constellation of all RVA isolates, it could be concluded that approximately one quarter had likely arisen from reassortment events in vivo among RVAs of 'usual' genotypes. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03048608
Volume :
161
Issue :
10
Database :
Academic Search Index
Journal :
Archives of Virology
Publication Type :
Academic Journal
Accession number :
117761537
Full Text :
https://doi.org/10.1007/s00705-016-2969-6