Polyphosphate kinase 1 (PPK1) is a pathogenesis determinant in Campylobacter jejuni
Campylobacter jejuni (C. jejuni) is the leading cause of bacterial gastroenteritis in the developed world. Despite the prevalence of C. jejuni as a human pathogen, relatively little is known about it's precise pathogenesis mechanisms, particularly in comparison to other well-studied enteric pat...
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ndltd-UBC-oai-circle.library.ubc.ca-2429-315472018-01-05T17:46:09Z Polyphosphate kinase 1 (PPK1) is a pathogenesis determinant in Campylobacter jejuni Candon, Heather L. Campylobacter jejuni (C. jejuni) is the leading cause of bacterial gastroenteritis in the developed world. Despite the prevalence of C. jejuni as a human pathogen, relatively little is known about it's precise pathogenesis mechanisms, particularly in comparison to other well-studied enteric pathogens like E. coli and Salmonella spp. Altered expression of phosphate genes in a C.jejuni stringent response mutant, together with known correlations between the stringent response, polyphosphate (poly P), and virulence in other pathogens, led us to investigate the role of poly P in C. jejuni physiology and pathogenesis. All sequenced C. jejuni strains harbour a conserved putative polyphosphate kinase (PPK1) predicted to be principally responsible for poly P synthesis. We generated a targeted ppkl deletion mutant (Δppk1) in C. jejuni strain 81-176 and found that this mutant, as well as the ΔspoT stringent response mutant, exhibited low levels of poly P at all growth stages. In contrast, wild-type C. jejuni poly P levels increased significantly as the bacteria transitioned from log to stationary phase. Phenotypic analyses revealed that the Δppk1 mutant was defective for survival during osmotic shock and low-nutrient stress. However, certain phenotypes associated with ppk1 deletion in other bacteria (i.e., motility, oxidative stress) were unaffected in the C. jejuni mutant, which also displayed a surprising increase in biofilm formation. The C. jejuni Δppk1 mutant was also defective for the virulence-associated phenotype of intra-epithelial cell survival in a tissue culture infection model and exhibited a striking defect in dose-dependent chick colonization. These results indicate that poly P utilization and accumulation contribute significantly to C. jejuni pathogenesis and affect its ability to adapt to specific stresses and stringencies. Furthermore, our study demonstrates that poly P likely plays both similar and unique roles in C. jejuni compared to other bacteria, and that poly P metabolism is linked with stringent response mechanisms in C. jejuni. Science, Faculty of Microbiology and Immunology, Department of Graduate 2011-02-18T23:23:37Z 2011-02-18T23:23:37Z 2007 Text Thesis/Dissertation http://hdl.handle.net/2429/31547 eng For non-commercial purposes only, such as research, private study and education. Additional conditions apply, see Terms of Use https://open.library.ubc.ca/terms_of_use. University of British Columbia |
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English |
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Campylobacter jejuni (C. jejuni) is the leading cause of bacterial gastroenteritis in the developed world. Despite the prevalence of C. jejuni as a human pathogen, relatively little is known about it's precise pathogenesis mechanisms, particularly in comparison to other well-studied enteric pathogens like E. coli and Salmonella spp. Altered expression of phosphate genes in a C.jejuni stringent response mutant, together with known correlations between the stringent response, polyphosphate (poly P), and virulence in other pathogens, led us to investigate the role of poly P in C. jejuni physiology and pathogenesis. All sequenced C. jejuni strains harbour a conserved putative polyphosphate kinase (PPK1) predicted to be principally responsible for poly P synthesis. We generated a targeted ppkl deletion mutant (Δppk1) in C. jejuni strain 81-176 and found that this mutant, as well as the ΔspoT stringent response mutant, exhibited low levels of poly P at all growth stages. In contrast, wild-type C. jejuni poly P levels increased significantly as the bacteria transitioned from log to stationary phase. Phenotypic analyses revealed that the Δppk1 mutant was defective for survival during osmotic shock and low-nutrient stress. However, certain phenotypes associated with ppk1 deletion in other bacteria (i.e., motility, oxidative stress) were unaffected in the C. jejuni mutant, which also displayed a surprising increase in biofilm formation. The C. jejuni Δppk1 mutant was also defective for the virulence-associated phenotype of intra-epithelial cell survival in a tissue culture infection model and exhibited a striking defect in dose-dependent chick colonization. These results indicate that poly P utilization and accumulation contribute significantly to C. jejuni pathogenesis and affect its ability to adapt to specific stresses and stringencies. Furthermore, our study demonstrates that poly P likely plays both similar and unique roles in C. jejuni compared to other bacteria, and that poly P metabolism is linked with stringent response mechanisms in C. jejuni. === Science, Faculty of === Microbiology and Immunology, Department of === Graduate |
author |
Candon, Heather L. |
spellingShingle |
Candon, Heather L. Polyphosphate kinase 1 (PPK1) is a pathogenesis determinant in Campylobacter jejuni |
author_facet |
Candon, Heather L. |
author_sort |
Candon, Heather L. |
title |
Polyphosphate kinase 1 (PPK1) is a pathogenesis determinant in Campylobacter jejuni |
title_short |
Polyphosphate kinase 1 (PPK1) is a pathogenesis determinant in Campylobacter jejuni |
title_full |
Polyphosphate kinase 1 (PPK1) is a pathogenesis determinant in Campylobacter jejuni |
title_fullStr |
Polyphosphate kinase 1 (PPK1) is a pathogenesis determinant in Campylobacter jejuni |
title_full_unstemmed |
Polyphosphate kinase 1 (PPK1) is a pathogenesis determinant in Campylobacter jejuni |
title_sort |
polyphosphate kinase 1 (ppk1) is a pathogenesis determinant in campylobacter jejuni |
publisher |
University of British Columbia |
publishDate |
2011 |
url |
http://hdl.handle.net/2429/31547 |
work_keys_str_mv |
AT candonheatherl polyphosphatekinase1ppk1isapathogenesisdeterminantincampylobacterjejuni |
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