1. Proposal of serovars 17 and 18 of Actinobacillus pleuropneumoniae based on serological and genotypic analysis
- Author
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Bossé, Janine T, Li, Yanwen, Sárközi, Rita, Fodor, László, Lacouture, Sonia, Gottschalk, Marcelo, Casas Amoribieta, Maria, Angen, Øystein, Nedbalcova, Katerina, Holden, Matthew TG, Maskell, Duncan J, Tucker, Alexander W, Wren, Brendan W, Rycroft, Andrew N, Langford, Paul R, BRaDP1T consortium, Biotechnology and Biological Sciences Research Council (BBSRC), Pfizer Limited (UK), Biotechnology and Biological Sciences Research Council, University of St Andrews. School of Medicine, University of St Andrews. Infection and Global Health Division, University of St Andrews. Infection Group, and University of St Andrews. Biomedical Sciences Research Complex
- Subjects
0301 basic medicine ,Serotype ,Swine ,Biovar ,animal diseases ,Denmark ,DIVERSITY ,Polymerase Chain Reaction ,Actinobacillus Infections ,Genotype ,ASSAY ,Diagnostics ,Genetics ,Swine Diseases ,biology ,Structural gene ,Actinobacillus pleuropneumoniae ,General Medicine ,3. Good health ,PCR ,Serovar 18 ,SEROTYPE-2 ,Serovar 17 ,QR355 Virology ,Life Sciences & Biomedicine ,MULTIPLEX PCR ,0605 Microbiology ,DNA, Bacterial ,Canada ,GENES ,030106 microbiology ,Locus (genetics) ,QH426 Genetics ,Serogroup ,Microbiology ,Article ,03 medical and health sciences ,BRaDP1T consortium ,Animals ,BIOSYNTHESIS ,Veterinary Sciences ,Serotyping ,CAPSULAR POLYSACCHARIDES ,Gene ,QH426 ,Bacterial Capsules ,DNA Primers ,Whole genome sequencing ,QR355 ,Science & Technology ,General Veterinary ,IDENTIFICATION ,Whole Genome Sequencing ,0707 Veterinary Sciences ,STRAINS ,DAS ,biology.organism_classification ,bacterial infections and mycoses ,Capsule genes - Abstract
Highlights • Identification of two new serovars of Actinobacillus pleuropneumoniae. • Serological confirmation of specific reactivity with homologous antisera. • Characterization of the capsule loci of serovars 17 and 18. • Development of PCRs for molecular diagnostics., The aim of this study was to investigate isolates of Actinobacillus pleuropneumoniae previously designated serologically either as non-typable (NT) or as ‘K2:07’, which did not produce serovar-specific amplicons in PCR assays. We used whole genome sequencing to identify the capsule (CPS) loci of six previously designated biovar 1 NT and two biovar 1 ‘K2:O7’ isolates of A. pleuropneumoniae from Denmark, as well as a recent biovar 2 NT isolate from Canada. All of the NT isolates have the same six-gene type I CPS locus, sharing common cpsABC genes with serovars 2, 3, 6, 7, 8, 9, 11 and 13. The two ‘K2:O7’ isolates contain a unique three-gene type II CPS locus, having a cpsA gene similar to that of serovars 1, 4, 12, 14 and 15. The previously NT isolates share the same O-antigen genes, found between erpA and rpsU, as serovars 3, 6, 8, and 15. Whereas the ‘K2:O7’ isolates, have the same O-antigen genes as serovar 7, which likely contributed to their previous mis-identification. All of the NT and ‘K2:O7’ isolates have only the genes required for production of ApxII (apxIICA structural genes, and apxIBD export genes). Rabbit polyclonal antisera raised against representative isolates with these new CPS loci demonstrated distinct reactivity compared to the 16 known serovars. The serological and genomic results indicate that the isolates constitute new serovars 17 (previously NT) and 18 (previously ‘K2:O7’). Primers designed for amplification of specific serovar 17 and 18 sequences for molecular diagnostics will facilitate epidemiological tracking of these two new serovars of A. pleuropneumoniae.
- Published
- 2018