Prevalence and genetic diversity of Aichi virus strains in stool samples from community and hospitalized patients

被引:130
作者
Ambert-Balay, K. [1 ,3 ]
Lorrot, M. [2 ]
Bon, F. [1 ,3 ]
Giraudon, H. [1 ,3 ]
Kaplon, J. [1 ,3 ]
Wolfer, M. [2 ]
Lebon, P. [4 ]
Gendrel, D. [2 ]
Pothier, P. [1 ,3 ]
机构
[1] CHU Dijon, Virol Lab, CNR Virus Enter, Reference Lab Enter Viruses, F-21079 Dijon, France
[2] Ctr Hosp St Vincent de Paul, Serv Pediat, Paris, France
[3] UFR Med & Pharm, Dijon, France
[4] Ctr Hosp St Vincent de Paul, Virol Lab, Paris, France
关键词
D O I
10.1128/JCM.02140-07
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Aichi virus has been proposed as a causative agent of gastroenteritis. A total of 457 stool specimens from children hospitalized with acute diarrhea and 566 stool specimens from adults and children involved in 110 gastroenteritis outbreaks were screened for the presence of Aichi virus by reverse transcription-PCR (RT-PCR) amplification of the genomic region of the 3C and 3D (3CD) nonstructural proteins. Our results show a low incidence of Aichi virus in pediatric samples and the existence of mixed infections with other microbiological agents in some cases. From the outbreak survey, it appears that the presence of Aichi virus is an indicator of mixed infections causing gastroenteritis outbreaks and that it could be involved in half of the oyster-associated outbreaks. A second RT-PCR was developed to amplify a part of the VP1 gene. The phylogenetic analysis showed a good correlation between the two classifications based on 3CD and VP1 gene sequences and revealed the prevalence of genotype A in France. It also allowed us to partially describe an Aichi virus strain that could represent a new genotype, thus suggesting the existence of a certain diversity.
引用
收藏
页码:1252 / 1258
页数:7
相关论文
共 26 条
[1]   Rapid typing of human adenoviruses by a general PCR combined with restriction endonuclease analysis [J].
Allard, A ;
Albinsson, B ;
Wadell, G .
JOURNAL OF CLINICAL MICROBIOLOGY, 2001, 39 (02) :498-505
[2]   MOLECULAR-DETECTION AND IDENTIFICATION OF ENTEROVIRUSES USING ENZYMATIC AMPLIFICATION AND NUCLEIC-ACID HYBRIDIZATION [J].
CHAPMAN, NM ;
TRACY, S ;
GAUNTT, CJ ;
FORTMUELLER, U .
JOURNAL OF CLINICAL MICROBIOLOGY, 1990, 28 (05) :843-850
[3]   IDENTIFICATION OF GROUP-A ROTAVIRUS GENE-4 TYPES BY POLYMERASE CHAIN-REACTION [J].
GENTSCH, JR ;
GLASS, RI ;
WOODS, P ;
GOUVEA, V ;
GORZIGLIA, M ;
FLORES, J ;
DAS, BK ;
BHAN, MK .
JOURNAL OF CLINICAL MICROBIOLOGY, 1992, 30 (06) :1365-1373
[4]  
Glass RI, 2001, NOVART FDN SYMP, V238, P5
[5]   POLYMERASE CHAIN-REACTION AMPLIFICATION AND TYPING OF ROTAVIRUS NUCLEIC-ACID FROM STOOL SPECIMENS [J].
GOUVEA, V ;
GLASS, RI ;
WOODS, P ;
TANIGUCHI, K ;
CLARK, HF ;
FORRESTER, B ;
FANG, ZY .
JOURNAL OF CLINICAL MICROBIOLOGY, 1990, 28 (02) :276-282
[6]   Genogroup-specific PCR primers for detection of Norwalk-like viruses [J].
Kojima, S ;
Kageyama, T ;
Fukushi, S ;
Hoshino, FB ;
Shinohara, M ;
Uchida, K ;
Natori, K ;
Takeda, N ;
Katayama, K .
JOURNAL OF VIROLOGICAL METHODS, 2002, 100 (1-2) :107-114
[7]   Evaluation of a degenerate primer for the PCR detection of human caliciviruses - Brief report [J].
LeGuyader, F ;
Estes, MK ;
Hardy, ME ;
Neill, FH ;
Green, J ;
Brown, DWG ;
Atmar, RL .
ARCHIVES OF VIROLOGY, 1996, 141 (11) :2225-2235
[8]  
Noel JS, 1997, J MED VIROL, V52, P173, DOI 10.1002/(SICI)1096-9071(199706)52:2&lt
[9]  
173::AID-JMV10&gt
[10]  
3.0.CO