Abstract

BackgroundSalmonella enterica subsp. enterica serovar Dublin (S. Dublin), a cattle adapted serovar causes enteritis, and systemic disease in bovines. The invasive index of this serovar far exceeds that of the other serovars and human infections often present as fatal or highly resistant infections. In this, observational study, phenotypic properties of human and bovine-derived isolates of S. Dublin along with antibiogram of common antimicrobials were evaluated. The multiplex PCR confirmed isolates were genotyped using 7-gene legacy MLST. MIC assay was done by broth microdilution method. Previously published protocols were used to assess the motility, biofilm formation and morphotype. Vi antigen was agglutinated using commercial antiserum. Caenorhabditis elegans infection model was used to evaluate the virulence potiential. Phenotyping experiments were done in duplicates while virulence assay was done in triplicates. Whole-genome sequencing was used to predict the genes responsible for acquired resistance and a genotype-phenotype comparison was made.ResultsWe evaluated 96 bovine and 10 human isolates in this study. All the isolates belonged to ST10 in eBG53 and were negative for Vi-antigen. The swarming motility, biofilm formation and morphotype were variable in the isolates of both groups. Resistance to sulfamethoxazole, ampicillin, chloramphenicol, tetracycline was > 90% in animal isolates whereas resistance to sulfamethoxazole was > 70% in human isolates. MDR was also higher in animal isolates. Human isolates were significantly (P < 0.0001) more virulent than animal isolates on C. elegans infection model. The genomic comparison based on the core SNPs showed a high degree of homogeneity between the isolates. The carriage of IncA/C2 plasmid was seen as a typical feature of isolates from the bovine hosts.ConclusionHuman isolates showed more diversity in the phenotypic assays. Animal isolates showed a higher degree of antimicrobial resistance with greater MDR but human isolates formed more biofilm and had greater swarming motility as well as increased virulence to the nematode C. elegans. The carriage of IncA/C2 plasmid could contribute to the distinguishing feature of the bovine isolates. The tandem use of genotypic-phenotypic assays improves the understanding of diversity and differential behaviour of the same serovar from unrelated host sources.

Highlights

  • IntroductionDublin), a cattle adapted serovar causes enteritis, and systemic disease in bovines

  • Out of 108 isolates, 96 bovine and 10 human isolates were confirmed as Salmonella Dublin type by the multiplex PCR

  • Whole-genome sequence analysis of these isolates in Enterobase showed that these non-Dublin serovars were serovars Javiana and Agona

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Summary

Introduction

Dublin), a cattle adapted serovar causes enteritis, and systemic disease in bovines. Observational study, phenotypic properties of human and bovine-derived isolates of S. Dublin), cattle adapted serovar causes enteritis and/or systemic disease in bovine hosts [1]. It can infect other animals including humans [2]. Dublin is infrequently reported to cause foodborne outbreaks in humans [9]. This has been isolated from blood and sputum [10], pediatric or infant patients [11, 12], and cases of the hepatic abscess [13, 14]. The high altitude yaks are found to be positive for infections with this serovar [15]

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