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   Bacterial size matters: Multiple mechanisms controlling septum cleavage and diplococcus formation are critical for the virulence of the opportunistic pathogen Enterococcus faecalis  
   
نویسنده salamaga b. ,prajsnar t.k. ,jareño-martinez a. ,willemse j. ,bewley m.a. ,chau f. ,ben belkacem t. ,meijer a.h. ,dockrell d.h. ,renshaw s.a. ,mesnage s.
منبع plos pathogens - 2017 - دوره : 13 - شماره : 7
چکیده    Enterococcus faecalis is an opportunistic pathogen frequently isolated in clinical settings. this organism is intrinsically resistant to several clinically relevant antibiotics and can transfer resistance to other pathogens. although e. faecalis has emerged as a major nosocomial pathogen,the mechanisms underlying the virulence of this organism remain elusive. we studied the regulation of daughter cell separation during growth and explored the impact of this process on pathogenesis. we demonstrate that the activity of the atla peptidoglycan hydrolase,an enzyme dedicated to septum cleavage,is controlled by several mechanisms,including glycosylation and recognition of the peptidoglycan substrate. we show that the long cell chains of e. faecalis mutants are more susceptible to phagocytosis and are no longer able to cause lethality in the zebrafish model of infection. altogether,this work indicates that control of cell separation during division underpins the pathogenesis of e. faecalis infections and represents a novel enterococcal virulence factor. we propose that inhibition of septum cleavage during division represents an attractive therapeutic strategy to control infections. © 2017 salamaga et al.
آدرس krebs institute,university of sheffield,sheffield,united kingdom,department of molecular biology and biotechnology,university of sheffield,sheffield, United Kingdom, krebs institute,university of sheffield,sheffield,united kingdom,department of infection and immunity and cardiovascular disease,university of sheffield,sheffield,united kingdom,the bateson centre,university of sheffield,sheffield, United Kingdom, krebs institute,university of sheffield,sheffield,united kingdom,department of molecular biology and biotechnology,university of sheffield,sheffield, United Kingdom, institute of biology,leiden university,leiden, Netherlands, krebs institute,university of sheffield,sheffield,united kingdom,department of infection and immunity and cardiovascular disease,university of sheffield,sheffield, United Kingdom, infection,antimicrobiens,modélisation,evolution (iame),umr 1137 inserm,university paris diderot/university paris nord,paris, France, krebs institute,university of sheffield,sheffield,united kingdom,department of molecular biology and biotechnology,university of sheffield,sheffield, United Kingdom, institute of biology,leiden university,leiden, Netherlands, krebs institute,university of sheffield,sheffield,united kingdom,department of infection and immunity and cardiovascular disease,university of sheffield,sheffield,united kingdom,centre for inflammation research,university of edinburgh,edinburgh, United Kingdom, krebs institute,university of sheffield,sheffield,united kingdom,department of infection and immunity and cardiovascular disease,university of sheffield,sheffield, United Kingdom, krebs institute,university of sheffield,sheffield,united kingdom,department of molecular biology and biotechnology,university of sheffield,sheffield, United Kingdom
 
     
   
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