Campylobacter jejuni carbon starvation A (CstA) is involved in peptide utilization, motility and agglutination, and has a role in stimulation of dendritic cells

TY - JOUR

T1 - Campylobacter jejuni carbon starvation A (CstA) is involved in peptide utilization, motility and agglutination, and has a role in stimulation of dendritic cells

AU - Rasmussen, Janus Jagd

AU - Vegge, Christina Skovgaard

AU - Frøkiær, Hanne

AU - Howlett, R. M.

AU - Krogfelt, K. A.

AU - Kelly, D. J.

AU - Ingmer, Hanne

PY - 2013/8

Y1 - 2013/8

N2 - Campylobacter jejuni is the most frequent cause of severe gastroenteritis in the developed world. The major symptom of campylobacteriosis is inflammatory diarrhoea. The molecular mechanisms of this infection are poorly understood compared to those of less frequent disease-causing pathogens. In a previous study, we identified C. jejuni proteins that antibodies in human campylobacteriosis patients reacted with. One of the immunogenic proteins identified (Cj0917) displays homology to carbon starvation protein A (CstA) from Escherichia coli, where this protein is involved in the starvation response and peptide uptake. In contrast to many bacteria, C. jejuni relies on amino acids and organic acids for energy, but in vivo it is highly likely that peptides are also utilized, although their mechanisms of uptake are unknown. In this study, Biolog phenotype microarrays have been used to show that a DcstA mutant has a reduced ability to utilize a number of di-and tri-peptides as nitrogen sources. This phenotype was restored through genetic complementation, suggesting CstA is a peptide uptake system in C. jejuni. Furthermore, the DcstA mutant also displayed reduced motility and reduced agglutination compared to WT bacteria; these phenotypes were also restored through complementation. Murine dendritic cells exposed to UV-killed bacteria showed a reduced IL-12 production, but the same IL-10 response when encountering C. jejuni DcstA compared to the WT strain. The greater Th1 stimulation elicited by the WT as compared to DcstA mutant cells indicates an altered antigenic presentation on the surface, and thus an altered recognition of the mutant. Thus, we conclude that C. jejuni CstA is important not only for peptide utilization, but also it may influence host-pathogen interactions.

AB - Campylobacter jejuni is the most frequent cause of severe gastroenteritis in the developed world. The major symptom of campylobacteriosis is inflammatory diarrhoea. The molecular mechanisms of this infection are poorly understood compared to those of less frequent disease-causing pathogens. In a previous study, we identified C. jejuni proteins that antibodies in human campylobacteriosis patients reacted with. One of the immunogenic proteins identified (Cj0917) displays homology to carbon starvation protein A (CstA) from Escherichia coli, where this protein is involved in the starvation response and peptide uptake. In contrast to many bacteria, C. jejuni relies on amino acids and organic acids for energy, but in vivo it is highly likely that peptides are also utilized, although their mechanisms of uptake are unknown. In this study, Biolog phenotype microarrays have been used to show that a DcstA mutant has a reduced ability to utilize a number of di-and tri-peptides as nitrogen sources. This phenotype was restored through genetic complementation, suggesting CstA is a peptide uptake system in C. jejuni. Furthermore, the DcstA mutant also displayed reduced motility and reduced agglutination compared to WT bacteria; these phenotypes were also restored through complementation. Murine dendritic cells exposed to UV-killed bacteria showed a reduced IL-12 production, but the same IL-10 response when encountering C. jejuni DcstA compared to the WT strain. The greater Th1 stimulation elicited by the WT as compared to DcstA mutant cells indicates an altered antigenic presentation on the surface, and thus an altered recognition of the mutant. Thus, we conclude that C. jejuni CstA is important not only for peptide utilization, but also it may influence host-pathogen interactions.

U2 - 10.1099/jmm.0.059345-0

DO - 10.1099/jmm.0.059345-0

M3 - Journal article

SN - 0022-2615

VL - 62

SP - 1135

EP - 1143

JO - Journal of Medical Microbiology

JF - Journal of Medical Microbiology

IS - 8

ER -