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Proteomic Analysis of Rickettsia Parkeri Strain Portsmouth

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Journal Infect Immun
Date 2009 Oct 3
PMID 19797064
Citations 20
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Abstract

Rickettsia parkeri, a recently recognized pathogen of human, is one of several Rickettsia spp. in the United States that causes a spotted fever rickettsiosis. To gain insights into its biology and pathogenesis, we applied the proteomics approach to establish a two-dimensional gel proteome reference map and combined this technique with cell surface biotinylation to identify surface-exposed proteins of a low-passage isolate of R. parkeri obtained from a patient. We identified 91 proteins by matrix-assisted laser desorption ionization-tandem time of flight mass spectrometry. Of these, 28 were characterized as surface proteins, including virulence-related proteins (e.g., outer membrane protein A [OmpA], OmpB, beta-peptide, and RickA). Two-dimensional immunoblotting with serum from the R. parkeri-infected index patient was utilized to identify the immunoreactive proteins as potential targets for diagnosis and vaccine development. In addition to the known rickettsial antigens, OmpA and OmpB, we identified translation initiation factor 2, cell division protein FtsZ, and cysteinyl-tRNA synthetase as immunoreactive proteins. The proteome map with corresponding cell surface protein analysis and antigen detection will facilitate a better understanding of the mechanisms of rickettsial pathogenesis.

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References
1.
Jeng R, Goley E, DAlessio J, Chaga O, Svitkina T, Borisy G . A Rickettsia WASP-like protein activates the Arp2/3 complex and mediates actin-based motility. Cell Microbiol. 2004; 6(8):761-9. DOI: 10.1111/j.1462-5822.2004.00402.x. View

2.
Sunyakumthorn P, Bourchookarn A, Pornwiroon W, David C, Barker S, Macaluso K . Characterization and growth of polymorphic Rickettsia felis in a tick cell line. Appl Environ Microbiol. 2008; 74(10):3151-8. PMC: 2394910. DOI: 10.1128/AEM.00025-08. View

3.
Rosenfeld J, Capdevielle J, Guillemot J, Ferrara P . In-gel digestion of proteins for internal sequence analysis after one- or two-dimensional gel electrophoresis. Anal Biochem. 1992; 203(1):173-9. DOI: 10.1016/0003-2697(92)90061-b. View

4.
Bendtsen J, Nielsen H, von Heijne G, Brunak S . Improved prediction of signal peptides: SignalP 3.0. J Mol Biol. 2004; 340(4):783-95. DOI: 10.1016/j.jmb.2004.05.028. View

5.
Chao C, Chelius D, Zhang T, Mutumanje E, Ching W . Insight into the virulence of Rickettsia prowazekii by proteomic analysis and comparison with an avirulent strain. Biochim Biophys Acta. 2007; 1774(3):373-81. DOI: 10.1016/j.bbapap.2007.01.001. View