ArticleTransboundary and emerging diseases2022
Genomic characterization of Tenacibaculum maritimum O-antigen gene cluster and development of a multiplex PCR-based serotyping scheme.
Article in Transboundary and emerging diseases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed, 14 citations in OpenAlex.
- Diversity of biofilm architectures within the genusApplied and environmental microbiology · 2026Article
- Phenotypic, Genetic, and Virulence Characterization ofPathogens (Basel, Switzerland) · 2026Article
- Article
- Experimental Challenge of Chinook Salmon (Oncorhynchus tshawytscha) With Tenacibaculum maritimum and Tenacibaculum dicentrarchi Fulfils Koch's Postulates.Journal of fish diseases · 2025Article
- First complete genome sequence ofMicrobiology resource announcements · 2025Article
- LPS-Induced Mortality in Zebrafish: Preliminary Characterisation of Common Fish Pathogens.Microorganisms · 2023Article
- Genomics ofPathogens (Basel, Switzerland) · 2023Article
- The secretome of the fish pathogenFrontiers in cellular and infection microbiology · 2023Article
- Genomic characterization of Tenacibaculum maritimum O-antigen gene cluster and development of a multiplex PCR-based serotyping scheme.Transboundary and emerging diseases · 2022Article
- Tenacibaculosis caused byFrontiers in cellular and infection microbiology · 2022Review
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Authors and funding
8 authors at 4 institutions in 3 countries.
Funding
Abstract
Tenacibaculum maritimum is a devastating bacterial pathogen affecting a large variety of marine fish species. It is responsible for significant economic losses in aquaculture farms worldwide. Different typing methods have been proposed to analyse bacterial diversity and population structure. Serological heterogeneity has been observed and up to four different serotypes have been described so far. However, the underlying molecular factors remain unknown. By combining conventional serotyping and genome-wide association study, we identified the genomic loci likely involved in the O-antigen biosynthesis. This finding allowed the development of a robust multiplex PCR-based serotyping scheme able to detect subgroups within each serotype and therefore performs better than conventional serotyping. This scheme was successfully applied to a large number of isolates from worldwide origin and retrieved from a large variety of fish species. No obvious correlations were observed between the mPCR-based serotype and the host species or the geographic origin of the isolates. Strikingly, the distribution of mPCR-based serotypes does not follow the core genome phylogeny. Nevertheless, this simple and cost-effective mPCR-based serotyping method could be useful for different applications such as population structure analysis, disease surveillance, vaccine formulation and efficacy follow-up.
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Registered trials
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