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Virulence-associated Genome Sequences of Pasteurella canis and Unique Toxin Gene Prevalence of P. canis and Pasteurella multocida Isolated from Humans and Companion Animals
Comparative analysis of virulence factors (VFs) between and are lacking, although both cause zoonotic infections. We determined the virulence-associated genome sequence characteristics of and assessed the toxin gene prevalence unique to among clinical isolates of and . We selected 10 and 16 whole-ge...
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Published in: | Annals of laboratory medicine 2023-05, Vol.43 (3), p.263-272 |
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Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Comparative analysis of virulence factors (VFs) between
and
are lacking, although both cause zoonotic infections. We determined the virulence-associated genome sequence characteristics of
and assessed the toxin gene prevalence unique to
among clinical isolates of
and
.
We selected 10
and 16
whole-genome sequences (WGSs) from the National Center for Biotechnology database. The VFanalyzer tool was used to estimate
-characteristic VFs. Amino acid sequences of VFs were compared with multiple-aligned sequences. The genome structure containing
-characteristic and adjacent loci was compared to the corresponding
genome structure. After designing primer sequences and assessing their accuracy, we examined the gene prevalence of the
-characteristic VFs using PCR among clinical isolates of
and
.
Using VFanalyzer, we found virulence-associated cytolethal distending toxin (
)
loci common to all
WGSs that were not found in
WGSs. Similarities in the multiple alignments of CdtA-CdtB-CdtC amino acid sequences were found among the 10
WGSs. Shared or similar loci around
were identified between the
and
genome structures. The PCR-based
prevalence differed for
and
clinical isolates.
-specific
prevalence was identified among clinical isolates. These three loci may be unique toxin genes and promising targets for the rapid identification of
in clinical settings. |
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ISSN: | 2234-3806 2234-3814 |
DOI: | 10.3343/alm.2023.43.3.263 |