Premium
Epidemiologic applications of novel molecular methods to detect and differentiate small round structured viruses (Norwalk‐like viruses)
Author(s) -
Ando Tamie,
Jin Qi,
Gentsch Jon R.,
Monroe Stephan S.,
Noel Jacqueline S.,
Dowell Scott F.,
Cicirello Helen G.,
Kohn Melvin A.,
Glass Roger I.
Publication year - 1995
Publication title -
journal of medical virology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.782
H-Index - 121
eISSN - 1096-9071
pISSN - 0146-6615
DOI - 10.1002/jmv.1890470207
Subject(s) - virology , norwalk virus , biology , virus , norovirus
Abstract The molecular epidemiology of a large, multi‐state outbreak of oyster‐associated gastroenteritis [Kohn et al. (1995): Journal of the American Medical Association 273 :466–471. Dowell et al. (1995): Journal of Infectious Diseases 171 :1497–1503.] was examined using new methods to detect small round structured viruses (SRSVs) by reverse transcription‐polymerase chain reaction (RT‐PCR) and to characterize strains by Southern hybridization and nucleotide sequencing of 81‐bp of a PCR product amplified from the RNA polymerase gene. Of 37 stool specimens examined from patients in eight clusters of the multi‐state outbreak, 32 (86%) gave RT‐PCR products specific for SRSVs of PI‐A phylogenetic group. Nineteen PCR products from the eight clusters were confirmed to have the identical sequence, indicating that this large outbreak was attributed to a single strain of SRSV. In one of the eight clusters, five (63%) of eight patients had a mixed infection with a second SRSV strain that belonged to P2‐B phylogenetic group. Of 12 specimens from patients in five other outbreaks and one sporadic case which occurred at the same time as the multistate outbreak, 10 (83%) gave products specific for SRSVs representing four phylogenetic groups (PI‐A, PI‐B, P2‐A, and P2‐ B). The sequences of the PI‐A products from two outbreaks and that of the P2‐B product from another outbreak were identical to the P1‐A sequence from the eight clusters and the P2–6 sequence from the one cluster of the multistate outbreak, respectively. These results demonstrate the first application of these methods to enhance our understanding of the molecular epidemiology of SRSVs and provide answers of public health interest that could not have been obtained using classical epidemiologic methods alone. © 1995 Wiley‐Liss, lnc. This article is a US Government work and, as such, is in the public domain in the United States of America.