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Deletion of pic results in decreased virulence for a clinical isolate of Shigella flexneri 2a from China. | LitMetric

Deletion of pic results in decreased virulence for a clinical isolate of Shigella flexneri 2a from China.

BMC Microbiol

Department of Medical Microbiology and Parasitology, School of Basic Medical Sciences, Fudan University, Shanghai 200032, China.

Published: February 2013

AI Article Synopsis

  • Shigella is a significant cause of severe dysentery, with the severity depending on the virulence of specific strains, driven by complex genetic factors.
  • A new multiplex PCR assay was created to identify the S. flexneri 2a strain from rural China, leading to the isolation of different strains, including the notably less virulent strain SF51 that lacks the pic gene.
  • Research indicates that the pic gene enhances the pathogenicity of S. flexneri 2a by facilitating bacterial invasion into host cells and modifying inflammatory responses, with certain strains showing reduced virulence without it.

Article Abstract

Background: Shigella is a major pathogen responsible for bacillary dysentery, a severe form of shigellosis. Severity of the disease depends on the virulence of the infecting strain. Shigella pathogenicity is a multi-gene phenomenon, involving the participation of genes on an unstable large virulence plasmid and chromosomal pathogenicity islands.

Results: A multiplex PCR (mPCR) assay was developed to detect S. flexneri 2a from rural regions of Zhengding (Hebei Province, China). We isolated and tested 86 strains using our mPCR assay, which targeted the ipaH, ial and set1B genes. A clinical strain of S. flexneri 2a 51 (SF51) containing ipaH and ial, but lacking set1B was found. The virulence of this strain was found to be markedly decreased. Further testing showed that the SF51 strain lacked pic. To investigate the role of pic in S. flexneri 2a infections, a pic knockout mutant (SF301-∆ pic) and two complementation strains, SF301-∆ pic/pPic and SF51/pPic, were created. Differences in virulence for SF51, SF301-∆ pic, SF301-∆ pic/pPic, SF51/pPic and S. flexneri 2a 301 (SF301) were compared. Compared with SF301, both SF51 and SF301-∆ pic exhibited lower levels of Hela cell invasion and resulted in reduced keratoconjunctivitis, with low levels of tissue damage seen in murine eye sections. The virulence of SF301-∆ pic and SF51 was partially recovered in vitro and in vivo through the addition of a complementary pic gene.

Conclusions: The pic gene appears to be involved in an increase in pathogenicity of S. flexneri 2a. This gene assists with bacterial invasion into host cells and alters inflammatory reactions.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3626585PMC
http://dx.doi.org/10.1186/1471-2180-13-31DOI Listing

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