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Norovirus GII.Pe Genotype: Tracking a Foodborne Outbreak on a Cruise Ship Through Molecular Epidemiology, Brazil, 2014.
Morillo, Simone Guadagnucci; Luchs, Adriana; Cilli, Audrey; Ribeiro, Cibele Daniel; de Cássia Compagnoli Carmona, Rita; do Carmo Sampaio Tavares Timenetsky, Maria.
Affiliation
  • Morillo SG; Enteric Diseases Laboratory, Virology Center, Adolfo Lutz Institute, Avenida Dr Arnaldo, No 355, São Paulo, SP, CEP 01246-902, Brazil. sgmorillo@gmail.com.
  • Luchs A; Enteric Diseases Laboratory, Virology Center, Adolfo Lutz Institute, Avenida Dr Arnaldo, No 355, São Paulo, SP, CEP 01246-902, Brazil. driluchs@gmail.com.
  • Cilli A; Enteric Diseases Laboratory, Virology Center, Adolfo Lutz Institute, Avenida Dr Arnaldo, No 355, São Paulo, SP, CEP 01246-902, Brazil.
  • Ribeiro CD; Enteric Diseases Laboratory, Virology Center, Adolfo Lutz Institute, Avenida Dr Arnaldo, No 355, São Paulo, SP, CEP 01246-902, Brazil.
  • de Cássia Compagnoli Carmona R; Enteric Diseases Laboratory, Virology Center, Adolfo Lutz Institute, Avenida Dr Arnaldo, No 355, São Paulo, SP, CEP 01246-902, Brazil.
  • do Carmo Sampaio Tavares Timenetsky M; Enteric Diseases Laboratory, Virology Center, Adolfo Lutz Institute, Avenida Dr Arnaldo, No 355, São Paulo, SP, CEP 01246-902, Brazil. timenetsky.m@gmail.com.
Food Environ Virol ; 9(2): 142-148, 2017 06.
Article in En | MEDLINE | ID: mdl-27933493
Norovirus (NoV) is recognized as the most common cause of foodborne outbreaks. In 2014, an outbreak of acute gastroenteritis occurred on a cruise ship in Brazil, and NoV became the suspected etiology. Here we present the molecular identification of the NoV strains and the use of sequence analysis to determine modes of virus transmission. Food (cream cheese, tuna salad, grilled fish, orange mousse, and vegetables soup) and clinical samples were analyzed by ELISA, conventional RT-PCR, qRT-PCR, and sequencing. Genogroup GII NoV was identified by ELISA and conventional RT-PCR in fecal samples from 5 of 12 patients tested (41.7%), and in the orange mousse food sample by conventional RT-PCR and qRT-PCR. Two fecal GII NoV samples and the orange mousse GII NoV sample were successfully genotyped as GII.Pe (ORF 1), revealed 98.0-98.8% identities among them, and shared phylogenetically distinct cluster. Establishing the source of a NoV outbreak can be a challenging task. In this report, the molecular analysis of the partial RdRp NoV gene provided a powerful tool for genotyping (GII.Pe) and tracking of outbreak-related samples. In addition, the same fast and simple extraction methods applied to clinical samples could be successfully used for complex food matrices, and have the potential to be introduced in routine laboratories for screening foods for presence of NoV.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Caliciviridae Infections / Norovirus / Foodborne Diseases / Gastroenteritis Type of study: Screening_studies Limits: Adolescent / Adult / Aged / Aged80 / Child / Child, preschool / Female / Humans / Male / Middle aged Country/Region as subject: America do sul / Brasil Language: En Journal: Food Environ Virol Year: 2017 Document type: Article Affiliation country: Brazil Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Caliciviridae Infections / Norovirus / Foodborne Diseases / Gastroenteritis Type of study: Screening_studies Limits: Adolescent / Adult / Aged / Aged80 / Child / Child, preschool / Female / Humans / Male / Middle aged Country/Region as subject: America do sul / Brasil Language: En Journal: Food Environ Virol Year: 2017 Document type: Article Affiliation country: Brazil Country of publication: United States