Pseudomonas aeruginosa est une bactérie à Gram-négatif, pathogène et opportuniste, responsable de nombreuses et sévères infections chez l’homme. Ce microorganisme comme la plupart des organismes vivants a besoin de fer pour sa croissance ainsi que d’autres métaux biologiques comme le zinc, le cuivre, le nickel, le manganèse, le cobalt, le molybdène, le vanadium et d’autres. Afin d’acquérir le fer P. aeruginosa produit deux sidérophores majeurs, la pyoverdine (PVD), souvent considérée comme sidérophore principal, et la pyochéline (PCH). Lors de cette thèse nous avons pu démontrer les enzymes de biosynthèse de ces sidérophores adoptent une organisation spécifique aux pôles des bactéries. De plus, l’étude de la composition en métaux de P. aeruginosa dans différentes conditions de cultures a pu démontrer que la bactérie adapte sa concentration intracellulaire en métaux selon la composition du milieu extracellulaire. / Pseudomonas aeruginosa is an opportunistic Gram-negative pathogen. It is responsible for a wide range of human diseases. Iron is an essential element for this organism, like for nearly all other organisms. To a lower extent this organisms needs other metals such as zinc, copper,nickel, manganese and other for its survival. To acquire iron, P. aeruginosa secrets two major siderophores, pyoverdine (PVD) and pyochelin (PCH). During the thesis we have shown that the enzymes involved in the biosynthesis of theses siderophores adopt a specific localization at the bacterial cell poles. Furthermore, the study of the metal composition of P. aeruginosa in different growth conditions has shown that this bacterium is able to adaptits internal metal concentration to the extracellular metal availability.

The rising number of antibiotic resistant bacteria (ARB) may introduce to the post antibiotic era because they cause a loss of the therapeutic potential of antibiotics. For many years the important role of the natural environment as reservoir and dissemination pathway for ARB and responsible genes has been largely overlooked. However, especially aquatic ecosystems provide optimal conditions for the antibiotic resistance (AR) evolution: first, aquatic ecosystems are frequently affected by anthropogenic activities that cause multiple pollutions for example with heavy metals, that potentially cause co-selection of antibiotic- and heavy metal resistance. Second, aquatic ecosystems feature a dissemination pathway between human populations and natural environments via the urban water cycle. Water cycles between human associated environments (e.g. house holds and clinics) via waste water through waste water treatment plants into natural ecosystems (e.g. water bodies) and back as drinking water after purification. Third, ecosystem internal biotic interactions such as competition between bacteria and predation by the natural consumers seem to impact AR evolution sustainably. The present doctoral thesis focuses on the impact of abiotic and biotic factors on the proliferation of AR and responsible genes in natural aquatic environments, with special emphasis on (i) heavy metal driven co-selection of antibiotic and heavy metal resistance and (ii) on the impact of competition and predation on the evolution of AR. In order to quantify the risk of heavy metal driven co-selection for AR spread, I provide a first risk assessment based on literature values of environmental heavy metal loadings and related AR. Additionally, I developed a limit value named minimum co-selective concentration (MCC), which is the lowest concentration of a heavy metal that can potentially cause coselection in nature. It turned out that Cu, Zn, Ni, Hg, and Cd are suspected to be the main co-selecting heavy metals in the aquatic environment. I further investigated heavy metal driven co-selection of AR in a river ecosystem, the Western Bug River (Ukraine). I found indications for co-selection of resistance to five antibiotics (ciprofloxacin, gentamicin, amikacin, tobramycin, and cefepime) and two metals (Ni and Cd) caused by Ni- and Cd-levels. Both metals exceed their MCC for water samples and Cd additionally in sediments. As a second focal point the present work emphasis on ecological interactions effecting AR evolution. Currently three possible effects of ecological interactions on AR spread are discussed. First, environmental antibiotic levels are rather low, however they might favour ARB due to a competitive advantage. The reason is that even sublethal antibiotic levels reduce the growth of sensitive bacteria while resistant cells remain unaffected by the antibiotic action. Second, predation by protozoa is believed to impact conjugation between prey bacteria (and thus the transfer of DNA and potential resistance genes) by keeping bacteria in a growing stage that favours conjugation. Third, in order to escape predation by protozoa, bacteria evolved grazing defence mechanisms such as the formation of inedible biofilms, which can feedback on the evolution of AR. With an ordinary differential equation model, I tested the effect of low antibiotic levels and losses (e.g. due to predation) on the proliferation of ARB in a modelled planktonic system. In case that the model contains the mechanism that conjugation frequencies are highest during exponential growth, I found that (i) (grazing) losses enhance conjugation frequencies between bacteria and that (ii) medium levels of antibiotics and (grazing) losses favour resistant cells in the competition to sensitive bacteria. Biofilms are thought to be \'hot spots\' for conjugation but some plasmids have lower conjugation frequencies in biofilms compared to planktonic systems. As a first step, in order to discover predation effects on plasmid spread in plankton - biofilm systems I investigated grazing resistance of bacteria in grazing experiments. Both plankton and biofilm phenotypes were consumed, when exposed to their specialized grazer (either plankton-feeder or biofilmfeeder), whereas the other phenotype remained grazing-resistant and thus became the dominant prey type. Both predators together effectively control planktonic and biofilm prey. With regards to the spread of AR-genes via conjugation, I speculate that the feeding preference of the present predator can affect the invasion success of resistance plasmids in planktonic - biofilm systems. For dynamic systems, I assume that dynamics of predator and prey traits (plankton vs. biofilm-feeder and biofilm vs. planktonic prey) will lead to dynamics of conjugation frequencies in planktonic or biofilm bacteria. I assume that conjugation events are more frequent in the dominant prey type (plankton or biofilm). However, other factors such as pili-type of the plasmid (short and rigid pili, prefers conjugation in biofilms or long and flexible pili, prefers conjugation in plankton) might additionally influence plasmid invasion success in plankton - biofilm morphotypes.