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The origin of Vibrio cholerae influences uptake and persistence in the blue mussel Mytilus edulis
Högskolan Kristianstad, Sektionen för lärande och miljö. (Biomedicin, Avdelningen för Naturvetenskap)
Högskolan Kristianstad, Sektionen för lärande och miljö. (Biomedicin, Avdelningen för Naturvetenskap)ORCID-id: 0000-0002-8059-0156
Department of Molecular Biology, Umeå University.
National Institute of Cholera and Enteric Diseases, Kolkata, India.
Vise andre og tillknytning
2012 (engelsk)Inngår i: Journal of Shellfish Research, ISSN 0730-8000, E-ISSN 1943-6319, Vol. 31, nr 1, s. 87-92Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Vibrio cholerae may cause diarrheal diseases and wound infections, both of which have the potential to be fatal. Transmission to humans is often linked to consumption of contaminated shellfish/drinking water or dermal exposure to water (e.g. when swimming). In this study, we investigated whether different isolates of Vibrio cholerae differ in terms of accumulation, persistence, and viability when encountering blue mussels (Mytilus edulis). Mussel uptake and elimination of three different V. cholerae strains were compared: one fatal clinical non-O1/O139 isolate, one highly potent El Tor biotype, and one marine strain isolated from blue mussels. The results showed that the uptake of the marine strain was significantly higher than the clinical strain, but the elimination process of the marine strain was also more efficient. The El Tor strain was not at all ingested by the mussels. In addition, the survival of bacteria when incubated together with M. edulis hemocytes was tested in vitro. The viability of clinical strains was unaffected by the presence of hemocytes, and the marine strains were even more resistant and able to multiply. We conclude that the highly virulent El Tor biotype was not taken up by the mussels and could thereby escape the mussels' elimination process. The potentially fatal non-O1/O139 V. cholerae strain may accumulate in low numbers, but could be very persistent in mussels.

sted, utgiver, år, opplag, sider
2012. Vol. 31, nr 1, s. 87-92
Emneord [en]
mussel, Mytilus edulis, Vibrio cholerae, pathogenic, depuration, hemocytes
HSV kategori
Identifikatorer
URN: urn:nbn:se:hkr:diva-9251DOI: 10.2983/035.031.0111ISI: 000302846800011OAI: oai:DiVA.org:hkr-9251DiVA, id: diva2:524486
Tilgjengelig fra: 2012-05-02 Laget: 2012-05-02 Sist oppdatert: 2017-12-07bibliografisk kontrollert
Inngår i avhandling
1. Characterization and persistence of potential human pathogenic vibrios in aquatic environments
Åpne denne publikasjonen i ny fane eller vindu >>Characterization and persistence of potential human pathogenic vibrios in aquatic environments
2012 (engelsk)Doktoravhandling, med artikler (Annet vitenskapelig)
Abstract [en]

Vibrio spp., natural inhabitants of aquatic environments, are one of the most common causes of bacterial gastroenteritis in the world, being spread to humans via the ingestion of seafood, contaminated drinking water or exposure to seawater. The majority of Vibrio spp. are avirulent, but certain strains may sporadically be human pathogenic. Vibrio cholerae may cause cholera and fatal wound infections, Vibrio parahaemolyticus may cause gastroenteritis and Vibrio vulnificus may cause wound infections and sepsis. To expand current knowledge of the occurrence, ecological niche and persistence of potential human pathogenic Vibrio spp. in aquatic environments, occurrence and laboratory studies were performed. The seasonal variation of Vibrio spp. in clams and mussels from Mozambique and Sweden were studied, with isolated strains characterized and compared with those isolated from water samples collected in India. Results showed that the numbers of Vibrio spp. in Mozambican clams peaked during the warmer rainy season and that the dominating species was V. parahaemolyticus. Biochemical fingerprinting and virulence screened by PCR revealed a high similarity among strains from the different aquatic environments. However, isolate functional hemolytic analyses and antibiotic resistance patterns differed between strains; Swedish and Indian strains were less sensitive to the tested antibiotics and had a lower hemolytic capacity than those from Mozambique. Molecular analysis of bacterial DNA from Swedish mussels showed the presence of the three Vibrio spp. most commonly linked with human illness, as well as their associated virulence genes. The strains isolated from marine and clinical environments were equally and highly harmful to the tested eukaryotic cells. The persistence of clinical V. cholerae in aquatic environments was investigated in vivo. Strains were exposed to mussels, with bacterial uptake and elimination then examined. The mussels were able to avoid the most potent strain by complete closure of shells. The less potent strain was accumulated in mussel tissue in low levels and one marine control strain to a higher degree. Mussels eliminated the pathogenic strain less efficiently than they did the marine strain. One clinical and one marine strain were then exposed to 4°C for 21 days, with the temperature then increased to 20°C. The clinical strain was more prone to lose culturability than the marine strain at 4°C, the former performed significantly better in regaining culturability after the temperature up-shift. Subsequently, the persistence of the clinical strain in natural bottom sediment, incubating as above, was studied and results showed a similar decrease in culturable numbers in the sediment as in the water. As the clinical V. cholerae strains did not carry any of the standard set of virulence genes, the ability to change from non-culturable to culturable may be of great importance to strain pathogenicity. The results also show that natural bottom sediment may be a potential reservoir of human pathogenic Vibrio spp.

sted, utgiver, år, opplag, sider
Kristianstad: Kristianstad University, 2012
Emneord
Vibrio cholerae, Vibrio parahaemolyticus, Mozambique, Sweden, molluscs, occurrence, persistence, sediment, TCBS, PCR, PhP, antibiotic resistance
HSV kategori
Identifikatorer
urn:nbn:se:hkr:diva-9789 (URN)978-­‐91-­‐628-­‐8482-­‐6 (ISBN)
Tilgjengelig fra: 2012-10-17 Laget: 2012-10-17bibliografisk kontrollert

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