<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>66(4)</volume><submitter>Jarosz A</submitter><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Heat treatment is indispensable in fish canning to provide an acceptable shelf life. Its optimisation reduces the risk of the presence of &lt;i>Clostridium botulinum&lt;/i> spores, which could potentially cause botulism cases. This study evaluated canned fish samples for botulism neurotoxin (BoNT)-producing clostridia contamination and can bulging through microbiological contaminant growth. A new analytical approach was developed for detection of such clostridia and phenotypically similar species.&lt;h4>Material and methods&lt;/h4>A total of 70 canned fish samples suspected of exhibiting bulging features were analysed. Culture methods were used to detect clostridia. The isolates obtained were evaluated on the basis of the exhibited phenotypic characteristics. Also, PCRs were used for the detection of genes determining BoNT production (non-toxic non-haemagglutinin (&lt;i>ntnh&lt;/i>) genes) and the amplification of conservative 16S rDNA genes, which were Sanger sequenced. The obtained sequences were analysed using the Basic Local Alignment Search Tool.&lt;h4>Results&lt;/h4>&lt;i>Clostridium&lt;/i> genus species were isolated from 17 (24%) bulging and organoleptically changed samples. No &lt;i>ntnh&lt;/i> genes were present in these isolates; however, sequencing confirmed the presence of &lt;i>C. sporogenes&lt;/i>, a species with close affinity to &lt;i>C. botulinum&lt;/i>.&lt;h4>Conclusion&lt;/h4>To eliminate the threat of foodborne botulism, laboratory diagnostic techniques must detect species of the &lt;i>Clostridium&lt;/i> genus and elucidate their ability to produce BoNTs. Although &lt;i>Clostridium botulinum&lt;/i> is the most common cause of botulism, the possibility may not be ignored that non-pathogenic &lt;i>Clostridium&lt;/i> species may acquire botulinum toxigenicity. The similarity between the isolated strains of &lt;i>C. sporogenes&lt;/i> and &lt;i>C. botulinum&lt;/i> should be incorporated in the optimisation of heat treatment to guarantee a sterilised, microbiologically safe product.</pubmed_abstract><journal>Journal of veterinary research</journal><pagination>605-611</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9945006</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Potential Risk of Botulinum Neurotoxin -producing Clostridia Occurrence in Canned Fish.</pubmed_title><pmcid>PMC9945006</pmcid><pubmed_authors>Kozak B</pubmed_authors><pubmed_authors>Goldsztejn M</pubmed_authors><pubmed_authors>Jarosz A</pubmed_authors><pubmed_authors>Grenda T</pubmed_authors><pubmed_authors>Kwiatek K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Potential Risk of Botulinum Neurotoxin -producing Clostridia Occurrence in Canned Fish.</name><description>&lt;h4>Introduction&lt;/h4>Heat treatment is indispensable in fish canning to provide an acceptable shelf life. Its optimisation reduces the risk of the presence of &lt;i>Clostridium botulinum&lt;/i> spores, which could potentially cause botulism cases. This study evaluated canned fish samples for botulism neurotoxin (BoNT)-producing clostridia contamination and can bulging through microbiological contaminant growth. A new analytical approach was developed for detection of such clostridia and phenotypically similar species.&lt;h4>Material and methods&lt;/h4>A total of 70 canned fish samples suspected of exhibiting bulging features were analysed. Culture methods were used to detect clostridia. The isolates obtained were evaluated on the basis of the exhibited phenotypic characteristics. Also, PCRs were used for the detection of genes determining BoNT production (non-toxic non-haemagglutinin (&lt;i>ntnh&lt;/i>) genes) and the amplification of conservative 16S rDNA genes, which were Sanger sequenced. The obtained sequences were analysed using the Basic Local Alignment Search Tool.&lt;h4>Results&lt;/h4>&lt;i>Clostridium&lt;/i> genus species were isolated from 17 (24%) bulging and organoleptically changed samples. No &lt;i>ntnh&lt;/i> genes were present in these isolates; however, sequencing confirmed the presence of &lt;i>C. sporogenes&lt;/i>, a species with close affinity to &lt;i>C. botulinum&lt;/i>.&lt;h4>Conclusion&lt;/h4>To eliminate the threat of foodborne botulism, laboratory diagnostic techniques must detect species of the &lt;i>Clostridium&lt;/i> genus and elucidate their ability to produce BoNTs. Although &lt;i>Clostridium botulinum&lt;/i> is the most common cause of botulism, the possibility may not be ignored that non-pathogenic &lt;i>Clostridium&lt;/i> species may acquire botulinum toxigenicity. The similarity between the isolated strains of &lt;i>C. sporogenes&lt;/i> and &lt;i>C. botulinum&lt;/i> should be incorporated in the optimisation of heat treatment to guarantee a sterilised, microbiologically safe product.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-04-04T14:17:23.299Z</modification><creation>2025-02-19T02:24:02.055Z</creation></dates><accession>S-EPMC9945006</accession><cross_references><pubmed>36846039</pubmed><doi>10.2478/jvetres-2022-0060</doi></cross_references></HashMap>