Affiliation:
1. Department of Pathology and Center for Biodefense and Emerging Infectious Diseases, University of Texas Medical Branch at Galveston, 301 University Blvd., Keiller Bldg., Galveston, Texas 77555-0609
Abstract
ABSTRACT
Members of the genus
Rickettsia
possess the ability to invade host cells and promptly escape from phagosomal vacuoles into the host cell cytosol, thereby avoiding destruction within the endosomal pathway. The mechanism underlying rickettsial phagosomal escape remains unknown, although the genomic sequences of several rickettsial species have allowed for the identification of four genes with potential membranolytic activities (
tlyA
,
tlyC
,
pat1
, and
pld
). This study was undertaken to determine which of the selected genes of
Rickettsia prowazekii
mediate the escape process. Quantitative ultrastructural analyses indicated that the period of active phagosomal escape was between 30 and 50 min postinfection. Reverse transcriptase PCR analyses determined that
tlyC
and
pld
were transcribed during the period of active phagosomal escape but that
tlyA
and
pat1
were not. The functionality of both
tlyC
and
pld
was determined by complementation studies of
Salmonella
, which replicates within endosomes. Complementation of
Salmonella
organisms with either
tlyC
or
pld
resulted in the escape of transformants from endosomal vacuoles into the host cell cytosol demonstrated by quantitative ultrastructural analyses. These data suggest a role for
tlyC
and
pld
in the process of phagosomal escape by
R. prowazekii
.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Cited by
131 articles.
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