Ricerca e caratterizzazione diVibrio parahaemolyticusin molluschi bibalvi vivi della Regione Sardegna
During 2013, 1079 mollusk samples collected from Sardinia ASLs (754 for Monitoring and 325 for market surveillance) were analyzed by IZS of Sassari. Samples were oysters (Crassostrea gigas,Ostrea edulis), clams (Tapes philippinarumanddecussatus) and mussels (Mytilus galloprovincialisandedulis). Samp...
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Other Authors: | , |
Format: | Doctoral or Postdoctoral Thesis |
Language: | Italian |
Published: |
Università degli studi di Sassari
2015
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Online Access: | http://hdl.handle.net/11388/250555 |
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author | MARCEDDU, Marta |
author2 | Marceddu, Marta MAZZETTE, Rina |
author_facet | MARCEDDU, Marta |
author_sort | MARCEDDU, Marta |
collection | CINECA IRIS Universitá Degli Studi di Sassari |
description | During 2013, 1079 mollusk samples collected from Sardinia ASLs (754 for Monitoring and 325 for market surveillance) were analyzed by IZS of Sassari. Samples were oysters (Crassostrea gigas,Ostrea edulis), clams (Tapes philippinarumanddecussatus) and mussels (Mytilus galloprovincialisandedulis). Samples were analyzed forV. parahaemolyticusby the ISO/TS 21872-1:2007. Strains were tested by PCR for the presence ofV. parahaemolyticusspecies-specific genes (toxR) and to detect the virulence genes (tdhandtrh). Group specific (GS)-PCR method, based on the sequence variation inToxRSgene, was also performed to detect the pandemic clone in correlation withtdhgene.V. parahemolyticusprevalence was 3.5% (38/1079). between positive samples, 35 (92.1%) were for Monitoring and 3 (7.9%) for official controls. tdh gene was identified In 5 (13%) samples, but there was no correlation withtoxRSgenes. Furthermore,trhgene was detected in 10 (26.3%) samples.V. parahaemolyticusis responsible of emerging public health problems. Reg. CE 2073/2005 does not fix specific criteria, however, recommend the application of good hygienic practices.V.parahaemolyticusprevalence is low. However, such results confirm that it is necessary acquire more knowledge aboutV. parahaemolyticusin Sardinia marine seawater. It would be appropriate to include this microorganism in the surveillance systems for gastrointestinal diseases and in monitoring programs in mollusk collection areas. |
format | Doctoral or Postdoctoral Thesis |
genre | Crassostrea gigas |
genre_facet | Crassostrea gigas |
id | ftsassariuniiris:oai:iris.uniss.it:11388/250555 |
institution | Open Polar |
language | Italian |
op_collection_id | ftsassariuniiris |
op_relation | http://hdl.handle.net/11388/250555 |
op_rights | info:eu-repo/semantics/openAccess |
publishDate | 2015 |
publisher | Università degli studi di Sassari |
record_format | openpolar |
spelling | ftsassariuniiris:oai:iris.uniss.it:11388/250555 2025-01-16T21:35:13+00:00 Ricerca e caratterizzazione diVibrio parahaemolyticusin molluschi bibalvi vivi della Regione Sardegna MARCEDDU, Marta Marceddu, Marta MAZZETTE, Rina 2015-02-20 http://hdl.handle.net/11388/250555 ita ita Università degli studi di Sassari http://hdl.handle.net/11388/250555 info:eu-repo/semantics/openAccess Vibrio parahaemolyticu molluschi bivalvi prevalenza caratterizzazione Settore VET/04 - Ispezione degli Alimenti di Origine Animale info:eu-repo/semantics/doctoralThesis 2015 ftsassariuniiris 2024-03-15T04:08:48Z During 2013, 1079 mollusk samples collected from Sardinia ASLs (754 for Monitoring and 325 for market surveillance) were analyzed by IZS of Sassari. Samples were oysters (Crassostrea gigas,Ostrea edulis), clams (Tapes philippinarumanddecussatus) and mussels (Mytilus galloprovincialisandedulis). Samples were analyzed forV. parahaemolyticusby the ISO/TS 21872-1:2007. Strains were tested by PCR for the presence ofV. parahaemolyticusspecies-specific genes (toxR) and to detect the virulence genes (tdhandtrh). Group specific (GS)-PCR method, based on the sequence variation inToxRSgene, was also performed to detect the pandemic clone in correlation withtdhgene.V. parahemolyticusprevalence was 3.5% (38/1079). between positive samples, 35 (92.1%) were for Monitoring and 3 (7.9%) for official controls. tdh gene was identified In 5 (13%) samples, but there was no correlation withtoxRSgenes. Furthermore,trhgene was detected in 10 (26.3%) samples.V. parahaemolyticusis responsible of emerging public health problems. Reg. CE 2073/2005 does not fix specific criteria, however, recommend the application of good hygienic practices.V.parahaemolyticusprevalence is low. However, such results confirm that it is necessary acquire more knowledge aboutV. parahaemolyticusin Sardinia marine seawater. It would be appropriate to include this microorganism in the surveillance systems for gastrointestinal diseases and in monitoring programs in mollusk collection areas. Doctoral or Postdoctoral Thesis Crassostrea gigas CINECA IRIS Universitá Degli Studi di Sassari |
spellingShingle | Vibrio parahaemolyticu molluschi bivalvi prevalenza caratterizzazione Settore VET/04 - Ispezione degli Alimenti di Origine Animale MARCEDDU, Marta Ricerca e caratterizzazione diVibrio parahaemolyticusin molluschi bibalvi vivi della Regione Sardegna |
title | Ricerca e caratterizzazione diVibrio parahaemolyticusin molluschi bibalvi vivi della Regione Sardegna |
title_full | Ricerca e caratterizzazione diVibrio parahaemolyticusin molluschi bibalvi vivi della Regione Sardegna |
title_fullStr | Ricerca e caratterizzazione diVibrio parahaemolyticusin molluschi bibalvi vivi della Regione Sardegna |
title_full_unstemmed | Ricerca e caratterizzazione diVibrio parahaemolyticusin molluschi bibalvi vivi della Regione Sardegna |
title_short | Ricerca e caratterizzazione diVibrio parahaemolyticusin molluschi bibalvi vivi della Regione Sardegna |
title_sort | ricerca e caratterizzazione divibrio parahaemolyticusin molluschi bibalvi vivi della regione sardegna |
topic | Vibrio parahaemolyticu molluschi bivalvi prevalenza caratterizzazione Settore VET/04 - Ispezione degli Alimenti di Origine Animale |
topic_facet | Vibrio parahaemolyticu molluschi bivalvi prevalenza caratterizzazione Settore VET/04 - Ispezione degli Alimenti di Origine Animale |
url | http://hdl.handle.net/11388/250555 |