Romero-Saavedra Felipe, Laverde Diana, Budin-Verneuil Aurélie, Muller Cécile, Bernay Benoit, Benachour Abdellah, Hartke Axel, Huebner Johannes
Division of Infectious Diseases, Department of Medicine, University Medical Center Freiburg, Freiburg, Germany; EA4655 U2RM Stress/Virulence, University of Caen Lower-Normandy, Caen, France.
EA4655 U2RM Stress/Virulence, University of Caen Lower-Normandy, Caen, France.
PLoS One. 2015 Aug 31;10(8):e0136625. doi: 10.1371/journal.pone.0136625. eCollection 2015.
Enterococcus faecium and faecalis are Gram-positive opportunistic pathogens that have become leading causes of nosocomial infections over the last decades. Especially multidrug resistant enterococci have become a challenging clinical problem worldwide. Therefore, new treatment options are needed and the identification of alternative targets for vaccine development has emerged as a feasible alternative to fight the infections caused by these pathogens.
We extrapolate the transcriptomic data from a mice peritonitis infection model in E. faecalis to identify putative up-regulated surface proteins under infection conditions in E. faecium. After the bionformatic analyses two metal binding lipoproteins were identified to have a high homology (>72%) between the two species, the manganese ABC transporter substrate-binding lipoprotein (PsaAfm,) and the zinc ABC transporter substrate-binding lipoprotein (AdcAfm). These candidate lipoproteins were overexpressed in Escherichia coli and purified. The recombinant proteins were used to produce rabbit polyclonal antibodies that were able to induce specific opsonic antibodies that mediated killing of the homologous strain E. faecium E155 as well as clinical strains E. faecium E1162, Enterococcus faecalis 12030, type 2 and type 5. Mice were passively immunized with the antibodies raised against recombinant lipoproteins, showing significant reduction of colony counts in mice livers after the bacterial challenge and demonstrating the efficacy of these metal binding lipoproteins as promising vaccine candidates to treat infections caused by these enterococcal pathogens.
Overall, our results demonstrate that these two metal binding lipoproteins elicited specific, opsonic and protective antibodies, with an extensive cross-reactivity and serotype-independent coverage among these two important nocosomial pathogens. Pointing these two protein antigens as promising immunogens, that can be used as single components or as carrier proteins together with polysaccharide antigens in vaccine development against enterococcal infections.
粪肠球菌和屎肠球菌是革兰氏阳性机会致病菌,在过去几十年中已成为医院感染的主要原因。特别是多重耐药肠球菌已成为全球具有挑战性的临床问题。因此,需要新的治疗选择,而鉴定疫苗开发的替代靶点已成为对抗这些病原体引起的感染的可行替代方案。
我们外推了粪肠球菌小鼠腹膜炎感染模型的转录组数据,以鉴定屎肠球菌感染条件下假定上调的表面蛋白。经过生物信息学分析,确定了两种金属结合脂蛋白在这两个物种之间具有高度同源性(>72%),即锰ABC转运体底物结合脂蛋白(PsaAfm)和锌ABC转运体底物结合脂蛋白(AdcAfm)。这些候选脂蛋白在大肠杆菌中过表达并纯化。重组蛋白用于制备兔多克隆抗体,这些抗体能够诱导特异性调理抗体,介导对同源菌株屎肠球菌E155以及临床菌株屎肠球菌E1162、粪肠球菌12030、2型和5型的杀伤。用针对重组脂蛋白产生的抗体对小鼠进行被动免疫,在细菌攻击后小鼠肝脏中的菌落计数显著减少,证明了这些金属结合脂蛋白作为治疗这些肠球菌病原体引起的感染的有前景的疫苗候选物的有效性。
总体而言,我们的结果表明,这两种金属结合脂蛋白引发了特异性、调理和保护性抗体,在这两种重要的医院病原体之间具有广泛的交叉反应性和血清型无关的覆盖范围。指出这两种蛋白质抗原是有前景的免疫原,可在针对肠球菌感染的疫苗开发中用作单一成分或与多糖抗原一起用作载体蛋白。