Characterization of human rotavirus genotype P[8]G5 from Brazil by probe-hybridization and sequence

被引:48
作者
Alfieri, AA
Leite, JPG
Nakagomi, O
Kaga, E
Woods, PA
Glass, RI
Gentsch, JR
机构
[1] CTR DIS CONTROL & PREVENT,VIRAL GASTROENTERITIS SECT,DIV VIRAL & RICKETTSIAL DIS,ATLANTA,GA 30333
[2] LONDRINA STATE UNIV,LAB ANIM VIROL,LONDRINA,BRAZIL
[3] INST OSWALDO CRUZ,DEPT VIROL,BR-20001 RIO JANEIRO,BRAZIL
[4] AKITA UNIV,SCH MED,DEPT MICROBIOL,AKITA 010,JAPAN
关键词
D O I
10.1007/BF01718636
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We report the molecular characterization of rotavirus genotype P[8]G5 strains found in fecal specimens collected in four different regions of Brazil, using digoxigenin (dig)-labeled oligonucleotide probes, sequence analysis, and RNA-RNA hybridization. The closest sequence relationships of the neutralization antigens of these strains were to the VP4 protein of P1A[8]G1 strain KU (93.3% identity in amino acids 11 to 282) and to the VP7 protein of G serotype 5 strain OSU (87.6% identity in amino acids 8 to 232). Based on VP7 sequence differences, we designed dig-probes that allowed us to discriminate porcine OSU-like strains from G5 strains isolated from Brazilian infants. The genetic relationships of two P[8]G5 isolates to other rotavirus genogroups were analyzed by RNA-RNA hybridization with [P-32]-GTP probes representative of serotypes P1A[8]G1 (Wa), P[8]G3 (AU17), and P9[7]G5 (OSU). The Brazilian P[8]G5 strains showed sequence homology with genes of Wa-like and OSU-like strains, suggesting that these two strains were naturally occurring reassortants between members of the Wa and porcine rotavirus genogroups. The identification of these strains in diverse geographic areas of Brazil underscores their stability and demonstrates the emergence of clinically important rotavirus diarrhea strains by reassortment.
引用
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页码:2353 / 2364
页数:12
相关论文
共 38 条
[1]   DETECTION AND DIFFERENTIATION OF ANTIGENICALLY DISTINCT SMALL ROUND-STRUCTURED VIRUSES (NORWALK-LIKE VIRUSES) BY REVERSE TRANSCRIPTION PCR AND SOUTHERN HYBRIDIZATION [J].
ANDO, T ;
MONROE, SS ;
GENTSCH, JR ;
JIN, Q ;
LEWIS, DC ;
GLASS, RI .
JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (01) :64-71
[2]   A SEROTYPE-10 HUMAN ROTAVIRUS [J].
BEARDS, G ;
XU, L ;
BALLARD, A ;
DESSELBERGER, U ;
MCCRAE, MA .
JOURNAL OF CLINICAL MICROBIOLOGY, 1992, 30 (06) :1432-1435
[3]   TEMPORAL AND GEOGRAPHICAL DISTRIBUTIONS OF HUMAN ROTAVIRUS SEROTYPES, 1983 TO 1988 [J].
BEARDS, GM ;
DESSELBERGER, U ;
FLEWETT, TH .
JOURNAL OF CLINICAL MICROBIOLOGY, 1989, 27 (12) :2827-2833
[4]   EPIDEMIOLOGY OF ROTAVIRUS SEROTYPES IN MELBOURNE, AUSTRALIA, FROM 1973 TO 1989 [J].
BISHOP, RF ;
UNICOMB, LE ;
BARNES, GL .
JOURNAL OF CLINICAL MICROBIOLOGY, 1991, 29 (05) :862-868
[5]   SEROLOGICAL AND GENOMIC CHARACTERIZATION OF L338, A NOVEL EQUINE GROUP-A ROTAVIRUS G-SEROTYPE [J].
BROWNING, GF ;
CHALMERS, RM ;
FITZGERALD, TA ;
SNODGRASS, DR .
JOURNAL OF GENERAL VIROLOGY, 1991, 72 :1059-1064
[6]   PHENOTYPES OF ROTAVIRUS REASSORTANTS DEPEND UPON THE RECIPIENT GENETIC BACKGROUND [J].
CHEN, DY ;
BURNS, JW ;
ESTES, MK ;
RAMIG, RF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (10) :3743-3747
[7]   CHARACTERIZATION OF ROTAVIRUS STRAINS FROM NEWBORNS IN NEW-DELHI, INDIA [J].
DAS, BK ;
GENTSCH, JR ;
CICIRELLO, HG ;
WOODS, PA ;
GUPTA, A ;
RAMACHANDRAN, M ;
KUMAR, R ;
BHAN, MK ;
GLASS, RI .
JOURNAL OF CLINICAL MICROBIOLOGY, 1994, 32 (07) :1820-1822
[8]   A COMPREHENSIVE SET OF SEQUENCE-ANALYSIS PROGRAMS FOR THE VAX [J].
DEVEREUX, J ;
HAEBERLI, P ;
SMITHIES, O .
NUCLEIC ACIDS RESEARCH, 1984, 12 (01) :387-395
[9]   SEROTYPIC AND GENOTYPIC CHARACTERIZATION OF HUMAN SEROTYPE-10 ROTAVIRUSES FROM ASYMPTOMATIC NEONATES [J].
DUNN, SJ ;
GREENBERG, HB ;
WARD, RL ;
NAKAGOMI, O ;
BURNS, JW ;
VO, PT ;
PAX, KA ;
DAS, M ;
GOWDA, K ;
RAO, CD .
JOURNAL OF CLINICAL MICROBIOLOGY, 1993, 31 (01) :165-169
[10]   ROTAVIRUS GENE STRUCTURE AND FUNCTION [J].
ESTES, MK ;
COHEN, J .
MICROBIOLOGICAL REVIEWS, 1989, 53 (04) :410-449