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Published on: July 8, 2011
The ability to replicate in macrophages is conserved between Yersinia pestis and Yersinia pseudotuberculosis
1Department of Molecular Genetics and Microbiology, Center for Infectious Diseases, State University of New York at Stony Brook, Stony Brook, NY 11794-5222, USA.
Abstract:
Yersinia pestis, the agent of plague, has arisen from a less virulent pathogen, Yersinia pseudotuberculosis, by a rapid evolutionary process. Although Y. pestis displays a large number of virulence phenotypes, it is not yet clear which of these phenotypes descended from Y. pseudotuberculosis and which were acquired independently. Y. pestis is known to replicate in macrophages, but there is no consensus in the literature on whether Y. pseudotuberculosis shares this property. We investigated whether the ability to replicate in macrophages is common to Y. pestis and Y. pseudotuberculosis or is a unique phenotype of Y. pestis. We also examined whether a chromosomal type III secretion system (TTSS) found in Y. pestis is present in Y. pseudotuberculosis and whether this system is important for replication of Yersinia in macrophages. A number of Y. pestis and Y. pseudotuberculosis strains of different biovars and serogroups, respectively, were tested for the ability to replicate in primary murine macrophages. Two Y. pestis strains (EV766 and KIM10(+)) and three Y. pseudotuberculosis strains (IP2790c, IP2515c, and IP2666c) were able to replicate in macrophages with similar efficiencies. Only one of six strains tested, the Y. pseudotuberculosis YPIII(p(-)) strain, was defective for intracellular replication. Thus, the ability to replicate in macrophages is conserved in Y. pestis and Y. pseudotuberculosis. Our results also indicate that a homologous TTSS is present on the chromosomes of Y. pestis and Y. pseudotuberculosis and that this secretion system is not required for replication of these bacteria in macrophages.
Insights
The ability of Yersinia bacteria to replicate within macrophages is conserved between Yersinia pestis and Yersinia pseudotuberculosis. A chromosomal type III secretion system (TTSS) is present in both species but not required for intracellular replication.
Area of Science:
- Microbiology
- Evolutionary Biology
- Pathogen Research
Background:
- Yersinia pestis, the causative agent of plague, evolved from Yersinia pseudotuberculosis.
- Key virulence factors distinguishing Y. pestis are not fully understood.
- The capacity of Yersinia species to replicate within macrophages is debated.
Purpose of the Study:
- To determine if macrophage replication is a shared or unique phenotype of Yersinia pestis.
- To investigate the presence and role of a chromosomal type III secretion system (TTSS) in Yersinia macrophage replication.
Main Methods:
- Testing multiple strains of Y. pestis and Y. pseudotuberculosis for intracellular replication in primary murine macrophages.
- Analyzing the presence of homologous chromosomal type III secretion systems (TTSS) in these strains.
Main Results:
- Both Y. pestis and Y. pseudotuberculosis strains demonstrated efficient replication within macrophages.
- A chromosomal type III secretion system (TTSS) was found to be homologous in both species.
- The TTSS was not essential for the intracellular replication of Yersinia in macrophages.
Conclusions:
- Macrophage replication is a conserved trait in Yersinia pestis and Yersinia pseudotuberculosis.
- The chromosomal type III secretion system (TTSS) is present in both species but does not mediate intracellular replication.
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