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Published on: August 11, 2014
Cooperation of Adhesin Alleles in Salmonella-Host Tropism
Leon De Masi1, Min Yue1, Changmin Hu1
1Department of Pathobiology, University of Pennsylvania, School of Veterinary Medicine, Philadelphia, Pennsylvania, USA.
Abstract:
Allelic combinations and host specificities for three fimbrial adhesins, FimH, BcfD, and StfH, were compared for 262 strains of Salmonella enterica serovar Newport, a frequent human and livestock pathogen. Like FimH, BcfD had two major alleles (designated A and B), whereas StfH had two allelic groups, each with two alleles (subgroup A1 and A2 and subgroup B1 and B2). The most prevalent combinations of FimH/BcfD/StfH alleles in S. Newport were A/A/A1 and B/B/B1. The former set was most frequently found in bovine and porcine strains, whereas the latter combination was most frequently found in environmental and human isolates. Bacteria genetically engineered to express Fim, Bcf, or Stf fimbriae on their surface were tested with the different alleles for binding to human, porcine, and bovine intestinal epithelial cells. The major allelic combinations with bovine and porcine strains (A/A/A1) or with human isolates (B/B/B1) provided at least two alleles capable of binding significantly better than the other alleles to an intestinal epithelial cell line from the respective host(s). However, each combination of alleles kept at least one allele mediating binding to an intestinal epithelial cell from another host. These findings indicated that allelic variation in multiple adhesins of S. Newport contributes to bacterial adaptation to certain preferential hosts without losing the capacity to maintain a broad host range. IMPORTANCESalmonella enterica remains a leading foodborne bacterial pathogen in the United States; infected livestock serve often as the source of contaminated food products. A study estimated that over a billion Salmonella gastroenteritis cases and up to 33 million typhoid cases occur annually worldwide, with 3.5 million deaths. Although many Salmonella strains with a broad host range present preferential associations with certain host species, it is not clear what determines the various levels of host adaptation. Here, causal properties of host associations were determined with allelic variants of three colonization factors of S. enterica serovar Newport, a most frequent zoonotic serovar. This is the first study that related not only individual but also a small group of host-associated gene variants with functional properties that cooperate to determine the level of host-adapted virulence. The detected associations should help to identify sources of Salmonella infections in both humans and animals.
Insights
Allelic variations in Salmonella enterica serovar Newport adhesins influence host specificity. Specific allele combinations promote adaptation to preferential hosts like cattle or humans, while maintaining a broad host range for this foodborne pathogen.
Area of Science:
- Microbiology
- Genetics
- Pathogen Host Interactions
Background:
- Salmonella enterica is a major foodborne pathogen, with livestock as a common source.
- Understanding host adaptation mechanisms in Salmonella is crucial for controlling infections.
- Salmonella enterica serovar Newport exhibits broad host range but also preferential associations.
Purpose of the Study:
- To investigate the role of allelic variations in three fimbrial adhesins (FimH, BcfD, StfH) of Salmonella enterica serovar Newport.
- To determine how these allelic combinations contribute to host specificity and adaptation.
- To identify the functional properties of gene variants cooperating in host-adapted virulence.
Main Methods:
- Comparative analysis of FimH, BcfD, and StfH alleles in 262 Salmonella enterica serovar Newport strains.
- Genetically engineered bacteria expressing different fimbrial adhesin alleles were used.
- Binding assays were performed using human, porcine, and bovine intestinal epithelial cells.
Main Results:
- Two major allelic combinations, A/A/A1 and B/B/B1, were prevalent in Salmonella enterica serovar Newport.
- The A/A/A1 combination was frequent in bovine and porcine strains, while B/B/B1 was found in human and environmental isolates.
- Specific allele combinations enhanced binding to host-specific intestinal cells, but retained binding capacity to other hosts.
Conclusions:
- Allelic variation in multiple adhesins of Salmonella enterica serovar Newport drives adaptation to preferential hosts.
- This allelic variation allows for host specialization without sacrificing the ability to infect a broad range of hosts.
- Findings aid in identifying sources of Salmonella infections in humans and animals.
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