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Molecular mechanism of horizontal gene transfer in pathogenic epsilon-proteobacteria

Antragstellerin Dr. Kerstin Stingl
Fachliche Zuordnung Parasitologie und Biologie der Erreger tropischer Infektionskrankheiten
Förderung Förderung von 2010 bis 2015
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 175974972
 
Erstellungsjahr 2015

Zusammenfassung der Projektergebnisse

As a neutrophilic bacterium, "Helicobacter pylori" is growth deficient under extremely acidic conditions. After overcoming the acid stress in the gastric lumen, the bacterium reaches its natural habitat with near neutral pH where it causes chronic gastritis. The bacterium shows an exceptionally high genetic variability that is mainly due to its natural competence, characterized by the capability to take up free DNA. During micro-aerobic growth significant competence development was observed. Comparative cultural and microscopic analysis showed that "H. pylori" was capable of regulating its transformation rate by several log levels. The dynamics were controlled by variation of the amount of cells exhibiting active DNA uptake over the outer membrane. The single cell analysis is based on the monitoring of uptake of covalently labelled fluorescent DNA in living cells. Single cell analysis showed that natural transformation of "H. pylori" was strongly influenced by pH. In this regard, pH values above 6.5 opened a competence window, in which competence development was triggered by the level of oxidative stress. These conclusions were drawn from the fact that the kinetics of competence development was influenced by different oxygen levels as well as by the presence of adenine. Furthermore, it was observed that previously active DNA uptake complexes were reversibly shut down below pH 6.5. In contrast, the addition of sub-lethal concentrations of the DNA-damaging agent ciprofloxacin or mitomycin C did not trigger competence development under the studied conditions. An oxygen-sensitive mutant lacking the gene coding for superoxide dismutase (sodB) displayed a higher competent fraction of cells than the wildtype under comparable conditions. In addition, the "sodB" mutant showed substantial growth problems and conversion into non-cultivable coccoid forms even under reduced oxygen concentration in liquid media, which was compensated by addition of adenine. This indicated that adenine acted as a radical quencher. Quantification of periplasmically located DNA in competent J99 wildtype cells revealed an outstanding medial imported DNA amount of around 350 kb per cell within 10 min, with maximal amounts of a chromosomal equivalent (1.6 Mb) in individual cells. The values for strain N6 were somewhat lower, but still impressive compared to other Gram-negative bacteria. It could be concluded that the pathogen's high genetic diversity is a consequence of its extremely high DNA uptake capacity, triggered by oxidative stress at neutral pH values. This might reflect the successful adaption of "H. pylori" to its natural environment, the gastric mucosa with near neutral pH values and probably increased oxygen stress exerted by the immune response of the host.

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