Genome divergence and increased virulence of outbreak associated Salmonella enterica subspecies enterica serovar Heidelberg

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作者
Linto Antony
Melissa Behr
Donald Sockett
Dale Miskimins
Nicole Aulik
Jane Christopher-Hennings
Eric Nelson
Marc W. Allard
Joy Scaria
机构
[1] South Dakota State University,Department of Veterinary and Biomedical Sciences
[2] South Dakota Center for Biologics Research and Commercialization,Wisconsin Veterinary Diagnostic Laboratory
[3] University of Wisconsin,Division of Microbiology, Office of Regulatory Science
[4] Center for Food Safety and Nutrition,undefined
[5] U.S. Food and Drug Administration,undefined
来源
Gut Pathogens | / 10卷
关键词
Outbreak; Genomic epidemiology; SNP; Fimbrial gene; Adhesion; Invasiveness; Multidrug resistance;
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摘要
Salmonella enterica serotype Heidelberg is primarily a poultry adapted serotype of Salmonella that can also colonize other hosts and cause human disease. In this study, we compared the genomes of outbreak associated non-outbreak causing Salmonella ser. Heidelberg strains from diverse hosts and geographical regions. Human outbreak associated strains in this study were from a 2015 multistate outbreak of Salmonella ser. Heidelberg involving 15 states in the United States which originated from bull calves. Our clinicopathologic examination revealed that cases involving Salmonella ser. Heidelberg strains were predominantly young, less than weeks-old, dairy calves. Pre-existing or concurrent disease was found in the majority of the calves. Detection of Salmonella ser. Heidelberg correlated with markedly increased death losses clinically comparable to those seen in herds infected with S. Dublin, a known serious pathogen of cattle. Whole genome based single nucleotide polymorphism based analysis revealed that these calf isolates formed a distinct cluster along with outbreak associated human isolates. The defining feature of the outbreak associated strains, when compared to older isolates of S. Heidelberg, is that all isolates in this cluster contained Saf fimbrial genes which are generally absent in S. Heidelberg. The acquisition of several single nucleotide polymorphisms and the gain of Saf fimbrial genes may have contributed to the increased disease severity of these Salmonella ser. Heidelberg strains.
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