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Morgene, M. F.

Publications and source records attributed to Morgene, M. F..

3 recordsLinked to original sources

Genetic transformation and cell division delay in competent Staphylococcus aureus

Natural competence for genetic transformation, considered as one of the three main mechanisms leading to horizontal gene transfer in bacteria, is able to promote evolution, through genomic plasticity, and foster antibiotic resistance and virulence factors spreading. Conserved machineries and actors required to perform genetic transformation have been shown to accumulate at different cellular localizations depending on the model organism considered. Here, we show in the human pathogen Staphylococcus aureus that DNA binding, uptake and recombination are spatially and temporally coordinated to ensure S. aureus genetic transformation. We also reveal that localization of genetic transformation proteins is dynamic and preferentially occurs in the vicinity of the division septum. We finally propose that S. aureus competent cells would initiate and then block cell division to ensure the success of genetic transformation before the final constriction of the cytokinetic ring.

microbiology↗

Microaerobic conditions and the complex regulation of natural competence in Staphylococcus aureus

To perform genetic transformation, one of the three main Horizontal Gene Transfer mechanisms leading to virulence and antibiotic resistance genes acquisition, bacteria need to enter a physiological differentiated state called natural competence. Diverse environmental and cellular cues have been shown to trigger complex regulatory pathways ultimately activating central competence regulators controlling the expression of the genetic transformation genes. Interestingly, new bacteria displaying such aptitude are often discovered, and one of the latest is the human pathogen Staphylococcus aureus. However, a clear understanding of the environmental signals, regulatory pathways and central regulators involved in the development of competence in S. aureus is not yet available. Here, using an original optimized protocol to naturally induce competence in planktonic cells, leading to improved transformation efficiencies (up to 5.10-6), we showed that the three putative central competence regulators identified in S. aureus are all essential for a complete development of competence. We also found that genes involved in genetic transformation can be divided in several classes depending on the regulators controlling their expression. In addition, we showed that oxygen availability is an important signal leading to competence development through the induction of one of the three central regulators. Our results demonstrate the complexity of competence development in S. aureus, in comparison to other historical model organisms. We anticipate our findings to be a starting point for proving the importance of natural competence and genetic transformation for S. aureus genomic plasticity. Furthermore, we also believe that our data will allow us to elucidate the environmental conditions leading to antibiotic resistance acquisitions in vivo, in this important human pathogen. Introductory paragraphStaphylococcus aureus has become over the years an important public health concern, due to a large range of infections and the emergence of outbreaks associated to antibiotic multi-resistant strains. S. aureus remarkable adaptive powers have been acquired through the acquisition of new genetic sequences, thanks to Horizontal Gene Transfer (HGT). The recent demonstration of the capacity of S. aureus to induce natural competence for genetic transformation prompted scientists to investigate this important mode of HGT in this new model organism in the field. Few key reports have already established that the development of competence in S. aureus might be complex, involving several potential master regulators, activated in response to multiple environmental signals and regulatory pathways. In this study, we deciphered, thanks to the design of an optimized protocol, the complexity of the regulatory pathways leading to the development of competence as well as its true potential for S. aureuss genomic plasticity in vivo. In addition, we clearly demonstrated that natural competence develops in response to oxygen limitation, a key environmental signal for a facultative anaerobe organism such as S. aureus.

microbiology↗

Construction and validation of EGFP-expressing Staphylococcus aureus clinical strains for adhesion and internalization assays on epithelial cells

BackgroundStaphylococcus aureus is both a major pathogen and a commensal bacterium in humans. It is able to adhere at the surface of epithelial cells of the anterior nares and can trigger its internalization inside these non-professional phagocytic cells. To better understand the interactions of clinical isolates with keratinocytes in the anterior nares, we developed and validated a one-step protocol expressing enhanced green fluorescent protein (EGFP) in S. aureus clinical strains with the aim to study adhesion to and internalization into mammalian cells.\n\nMethodsTwenty S. aureus clinical isolates belonging to clonal complexes 5, 8, 30, 45, 398 were selected for one-step transformation protocol with the EGFP-encoding plasmid pBSU101. EGFP expression was analysed by flow cytometry and confocal microscopy. Wild type and isogenic EGFP-expressing strains were compared for adhesion and internalization levels by using the HaCaT cell model.\n\nResultsTransformation was achieved in all the S. aureus strains regardless of their genetic background. The flow cytometry analysis showed that the mean proportion of EGFP-expressing bacteria was 97.2% ({+/-} 2.1) after 4h of incubation. Adhesion and internalization levels were similar in wild-type and isogenic EGFP-expressing S. aureus strains. Confocal laser scanning microscopy confirmed that EGFP-expressing S. aureus bacteria could be easily identified inside HaCaT keratinocytes.\n\nConclusionThis study reports an efficient protocol for expressing EGFP in S. aureus clinical strains and demonstrates that these EGFP-expressing strains are suitable for adhesion and internalization assays using HaCaT cells, which allows to perform static and dynamic in vitro studies of S. aureus colonization.

microbiology↗