2001
DOI: 10.2307/1592894
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Role of Campylobacter jejuni Potential Virulence Genes in Cecal Colonization

Abstract: Campylobacter jejuni, a common commensal in chickens, is one of the leading causes of bacterial gastroenteritis in humans worldwide. The aims of this investigation were twofold. First, we sought to determine whether mutations in the C. jejuni ciaB and pldA virulence-associated genes impaired the organism's ability to colonize chickens. Second, we sought to determine if inoculation of chicks with C. jejuni mutants could confer protection from subsequent challenge with the C. jejuni wild-type strain. The C. jeju… Show more

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Cited by 136 publications
(99 citation statements)
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“…The existence of this sequence similarity suggests that a similar gene sequence for a haemolytic PLA enzyme exists in C. concisus strains assigned to both PCR groups (genomospecies). A pldA mutant of C. coli was previously shown to have marked reduction in haemolytic activity when compared with the wild-type strain, suggesting a role for pldA as a virulence determinant in campylobacters (Grant et al, 1997), while a C. jejuni pldA mutant was reported to have an impaired ability for caecal colonization in chicken (Ziprin et al, 2001). Similar research with a H. pylori pldA mutant has been reported, suggesting that the H. pylori pldA phospholipase has a role in colonization of the gastric mucosa and possible tissue damage after colonization (Dorrell et al, 1999).…”
Section: Pcr Analysis Of Pla Genementioning
confidence: 99%
“…The existence of this sequence similarity suggests that a similar gene sequence for a haemolytic PLA enzyme exists in C. concisus strains assigned to both PCR groups (genomospecies). A pldA mutant of C. coli was previously shown to have marked reduction in haemolytic activity when compared with the wild-type strain, suggesting a role for pldA as a virulence determinant in campylobacters (Grant et al, 1997), while a C. jejuni pldA mutant was reported to have an impaired ability for caecal colonization in chicken (Ziprin et al, 2001). Similar research with a H. pylori pldA mutant has been reported, suggesting that the H. pylori pldA phospholipase has a role in colonization of the gastric mucosa and possible tissue damage after colonization (Dorrell et al, 1999).…”
Section: Pcr Analysis Of Pla Genementioning
confidence: 99%
“…Also, CiaB and other secreted proteins require functional flagella export apparatus for their secretion (Konkel et al, 2004;Dasti et al, 2010). The pldA gene encodes a protein involved in the synthesis of an outer membrane phospholipase that has also been related to cellular invasion (Ziprin et al, 2001). The plasmid pVir is associated with the ability of C. jejuni to adhere to and invade cells in vitro and has been shown to increase virulence in vivo (Bacon et al, 2000).…”
mentioning
confidence: 99%
“…Some genes are involved in Campylobacter adhesion and invasion. Four mutant strains derived from F38011, an excellent colonizer of chicken caeca, dnaJ, cadF, pldA and ciaB are incapable of colonizing the ceca [20,23,43,44]. cadF (Campylobacter adhesin to fibronectin) is an outer membrane protein, which encodes a protein that interacts with a host extracellular matrix protein fibronectin [31], and is required for Campylobacter adherence to and colonization of the host cell surface [20].…”
mentioning
confidence: 99%
“…cadF (Campylobacter adhesin to fibronectin) is an outer membrane protein, which encodes a protein that interacts with a host extracellular matrix protein fibronectin [31], and is required for Campylobacter adherence to and colonization of the host cell surface [20]. Other genes such as ciaB (Campylobacter invasive antigen B) [21,34] and pldA encoded outer membrane phospholipase A [34] are involved in host cell invasion and are important for caecal colonization [21,43]. The ciaB, pldA and dnaJ (heat shock protein) genes are important to caecal colonization and mutations of these genes severely limit the ability of the mutant strains to colonize the chicken caeca [20,43,44].…”
mentioning
confidence: 99%
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