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The depuration dynamics of oysters (Crassostrea gigas) artificially contaminated with hepatitis A virus and human adenovirus
Corrêa, Adriana de Abreu; Rigotto, Caroline; Moresco, Vanessa; Kleemann, Cristian Rafael; Teixeira, Adriano Luiz; Poli, Carlos Rogério; Simões, Cláudia Maria Oliveira; Barardi, Célia Regina Monte.
  • Corrêa, Adriana de Abreu; Universidade Federal de Santa Catarina. Laboratório de Virologia Aplicada. Florianópolis. BR
  • Rigotto, Caroline; Universidade Federal de Santa Catarina. Laboratório de Virologia Aplicada. Florianópolis. BR
  • Moresco, Vanessa; Universidade Federal de Santa Catarina. Laboratório de Virologia Aplicada. Florianópolis. BR
  • Kleemann, Cristian Rafael; Universidade Federal de Santa Catarina. Laboratório de Virologia Aplicada. Florianópolis. BR
  • Teixeira, Adriano Luiz; Universidade Federal de Santa Catarina. Laboratório de Virologia Aplicada. Florianópolis. BR
  • Poli, Carlos Rogério; Blue Water Aquaculture Ltda. Florianópolis. BR
  • Simões, Cláudia Maria Oliveira; Universidade Federal de Santa Catarina. Laboratório de Virologia Aplicada. Florianópolis. BR
  • Barardi, Célia Regina Monte; Universidade Federal de Santa Catarina. Laboratório de Virologia Aplicada. Florianópolis. BR
Mem. Inst. Oswaldo Cruz ; 107(1): 11-17, Feb. 2012. ilus, graf, tab
Article in English | LILACS | ID: lil-612800
ABSTRACT
Within the country of Brazil, Santa Catarina is a major shellfish producer. Detection of viral contamination is an important step to ensure production quality and consumer safety during this process. In this study, we used a depuration system and ultraviolet (UV) disinfection to eliminate viral pathogens from artificially infected oysters and analysed the results. Specifically, the oysters were contaminated with hepatitis A virus (HAV) or human adenovirus type 5 (HAdV5). After viral infection, the oysters were placed into a depuration tank and harvested after 48, 72 and 96 h. After sampling, various oyster tissues were dissected and homogenised and the viruses were eluted with alkaline conditions and precipitated with polyethylene glycol. The oyster samples were evaluated by cell culture methods, as well as polymerase chain reaction (PCR) and quantitative-PCR. Moreover, at the end of the depuration period, the disinfected seawater was collected and analysed by PCR. The molecular assays showed that the HAdV5 genome was present in all of the depuration time samples, while the HAV genome was undetectable after 72 h of depuration. However, viral viability tests (integrated cell culture-PCR and immunofluorescence assay) indicated that both viruses were inactivated with 96 h of seawater recirculation. In conclusion, after 96 h of UV treatment, the depuration system studied in this work purified oysters that were artificially contaminated with HAdV5 and HAV.
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Full text: Available Index: LILACS (Americas) Main subject: Ultraviolet Rays / Adenoviruses, Human / Disinfection / Aquaculture / Hepatitis A virus / Crassostrea / Food Microbiology Limits: Animals Language: English Journal: Mem. Inst. Oswaldo Cruz Journal subject: Tropical Medicine / Parasitology Year: 2012 Type: Article / Project document Affiliation country: Brazil Institution/Affiliation country: Blue Water Aquaculture Ltda/BR / Universidade Federal de Santa Catarina/BR

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Full text: Available Index: LILACS (Americas) Main subject: Ultraviolet Rays / Adenoviruses, Human / Disinfection / Aquaculture / Hepatitis A virus / Crassostrea / Food Microbiology Limits: Animals Language: English Journal: Mem. Inst. Oswaldo Cruz Journal subject: Tropical Medicine / Parasitology Year: 2012 Type: Article / Project document Affiliation country: Brazil Institution/Affiliation country: Blue Water Aquaculture Ltda/BR / Universidade Federal de Santa Catarina/BR