Laboratory strains of Bacillus anthracis exhibit pervasive alteration in expression of proteins related to sporulation under laboratory conditions relative to genetically related wild strains.

Autor: Leiser OP; Chemical and Biological Signature Science, Pacific Northwest National Laboratory, Richland, Washington, United States of America., Blackburn JK; Emerging Pathogens Institute, University of Florida, Gainesville, Florida, United States of America.; Spatial Epidemiology & Ecology Research Laboratory, Department of Geography, University of Florida, Gainesville, Florida, United States of America., Hadfield TL; Emerging Pathogens Institute, University of Florida, Gainesville, Florida, United States of America.; Spatial Epidemiology & Ecology Research Laboratory, Department of Geography, University of Florida, Gainesville, Florida, United States of America., Kreuzer HW; Chemical and Biological Signature Science, Pacific Northwest National Laboratory, Richland, Washington, United States of America., Wunschel DS; Chemical and Biological Signature Science, Pacific Northwest National Laboratory, Richland, Washington, United States of America., Bruckner-Lea CJ; Chemical and Biological Signature Science, Pacific Northwest National Laboratory, Richland, Washington, United States of America.
Jazyk: angličtina
Zdroj: PloS one [PLoS One] 2018 Dec 17; Vol. 13 (12), pp. e0209120. Date of Electronic Publication: 2018 Dec 17 (Print Publication: 2018).
DOI: 10.1371/journal.pone.0209120
Abstrakt: The spore forming pathogen Bacillus anthracis is the etiologic agent of anthrax in humans and animals. It cycles through infected hosts as vegetative cells and is eventually introduced into the environment where it generates an endospore resistant to many harsh conditions. The endospores are subsequently taken up by another host to begin the next cycle. Outbreaks of anthrax occur regularly worldwide in wildlife and livestock, and the potential for human infection exists whenever humans encounter infected animals. It is also possible to encounter intentional releases of anthrax spores, as was the case in October 2001. Consequently, it is important to be able to rapidly establish the provenance of infectious strains of B. anthracis. Here, we compare protein expression in seven low-passage wild isolates and four laboratory strains of B. anthracis grown under identical conditions using LC-MS/MS proteomic analysis. Of the 1,023 total identified proteins, 96 had significant abundance differences between wild and laboratory strains. Of those, 28 proteins directly related to sporulation were upregulated in wild isolates, with expression driven by Spo0A, CodY, and AbrB/ScoC. In addition, we observed evidence of changes in cell division and fatty acid biosynthesis between the two classes of strains, despite being grown under identical experimental conditions. These results suggest wild B. anthracis cells are more highly tuned to sporulate than their laboratory cousins, and this difference should be exploited as a method to differentiate between laboratory and low passage wild strains isolated during an anthrax outbreak. This knowledge should distinguish between intentional releases and exposure to strains in nature, providing a basis for the type of response by public health officials and investigators.
Competing Interests: The authors have declared that no competing interests exist.
Databáze: MEDLINE
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