Gallimore Chris I, Cheesbrough John S, Lamden Kenneth, Bingham Chris, Gray Jim J
Enteric, Respiratory and Neurological Virus Laboratory, Specialist and Reference Microbiology Division, Health Protection Agency Centre for Infections, Colindale, London, NW9 5HT, United Kingdom.
Int J Food Microbiol. 2005 Sep 15;103(3):323-30. doi: 10.1016/j.ijfoodmicro.2005.02.003.
The diversity of norovirus (NV) genotypes was investigated in persons who were ill with acute gastroenteritis associated with the consumption of oysters. Initial results from a commercial enzyme immunoassay (EIA) indicated a mixed NV genogroup I (GI) and II (GII) outbreak. A reverse-transcriptase (RT)-PCR for NVs was applied to nucleic acid extracted from faecal specimens collected from symptomatic cases. Using primers that amplified contiguous sequences in the ORF1/2 region of the NV genome and a hemi-nested PCR derived from this assay, three different GII and two GI NV genotypes were detected and the strains were characterised by DNA sequencing. Using this approach a recombinant NV genotype, rGII-3a (recombinant Harrow/Mexico) the predominant strain identified in several symptomatic cases from the outbreak, was detected and characterised. No other gastroenteric viruses, including rotavirus, astrovirus, sapovirus and adenovirus 40/41 were detected by RT-PCR and PCR.
对因食用牡蛎而患急性肠胃炎的患者的诺如病毒(NV)基因型多样性进行了调查。商业酶免疫测定(EIA)的初步结果表明,这是一起NV基因I组(GI)和II组(GII)混合暴发事件。将针对NV的逆转录酶(RT)-PCR应用于从有症状病例采集的粪便标本中提取的核酸。使用在NV基因组ORF1/2区域扩增连续序列的引物以及由此检测法衍生的半巢式PCR,检测到三种不同的GII和两种GI NV基因型,并通过DNA测序对菌株进行了表征。采用这种方法,检测并鉴定出一种重组NV基因型rGII-3a(重组哈罗/墨西哥株),它是此次暴发中几例有症状病例中鉴定出的主要菌株。通过RT-PCR和PCR未检测到其他胃肠病毒,包括轮状病毒、星状病毒、札幌病毒和腺病毒40/41。