Department of Microbiology and Botany, Faculty of Science, Zagazig University, Zagazig, Egypt.
J Appl Microbiol. 2021 Dec;131(6):2780-2792. doi: 10.1111/jam.15134. Epub 2021 Jun 3.
This study is aimed at characterization of both antimicrobial and anti-biofilm activity of R-pyocin from clinical Pseudomonas aeruginosa against Gram-positive pathogens including Staphylococcus aureus.
Pyocinogenic P. aeruginosa was detected using reverse-side method, and pyocinogeny typing was confirmed using revised-spotting method. Transmission electron microscopy (TEM) was used for morphological characterization of R-pyocin and for detection of changes in membrane of R-pyocin-treated S. aureus. SDS-PAGE analysis was used for detection of the molecular weight of R-pyocin protein-subunits and Poisson-killing-distribution assay for burst-size calculation. Lipotechoic-acid (LTA) adsorption-assay was used to confirm whether LTA in Gram-positive bacteria served as R-pyocin receptor. Moreover, R-pyocin production at 10-60°C was assessed herein. Host-range of activity of R-pyocin was tested against antimicrobial resistant (AMR) pathogens. The anti-biofilm activity of R-pyocin was detected against sensitive bacterial strains. Chemical, enzymatic, pH and thermo-stability of R-pyocin were evaluated. TEM micrographs revealed a typical morphology of myotailocins indicating the production of R-pyocin designated as RPU15. TEM revealed pores formation in S. aureus membrane, and bacteriophage-like plaques were obvious on plates of R-pyocin-treated S. aureus. R-pyocin activity was neutralized by LTA of S. aureus and Listeria monocytogenes. Pseudomonas aeruginosa PU15 produced ˜428 non-inducible R-pyocin particles. RPU15 sheath and tube protein-subunits exhibited a molecular weight of 38 and 23 kDa, respectively. RPU15 possessed activity against S. aureus, L. monocytogenes, Bacillus cereus and Candida albicans and reduced biofilm-biomasses of tested AMR strains.
Our results show the potential therapeutic use of R-pyocin due to its effectiveness on tested bacterial biofilms.
This is the first study that investigates antimicrobial and anti-biofilm activity of R-pyocin activity against S. aureus. R-pyocin shows new phenomenon of bacteriophage-like plaques. Our findings represent a future therapeutic agent targeting both methicillin-resistant and vancomycin-resistant S. aureus.
本研究旨在对临床铜绿假单胞菌来源的 R-噬菌体进行抗菌和抗生物膜活性的特征分析,以评估其对包括金黄色葡萄球菌在内的革兰氏阳性病原体的作用。
采用反向法检测产噬菌体铜绿假单胞菌,并用改良斑点法进行噬菌体生成分型确认。采用透射电子显微镜(TEM)观察 R-噬菌体的形态特征,并检测 R-噬菌体处理金黄色葡萄球菌后的细胞膜变化。SDS-PAGE 分析用于检测 R-噬菌体蛋白亚单位的分子量,泊松杀伤分布测定法用于计算爆发大小。通过脂磷壁酸(LTA)吸附实验,验证革兰氏阳性菌的 LTA 是否是 R-噬菌体的受体。此外,本文还评估了 R-噬菌体在 10-60°C 下的产生情况。检测 R-噬菌体对耐抗菌药物(AMR)病原体的作用范围。检测 R-噬菌体对敏感细菌菌株的抗生物膜活性。评估 R-噬菌体的化学、酶、pH 和热稳定性。TEM 照片显示了肌尾菌素的典型形态,表明 R-噬菌体的产生被指定为 RPU15。TEM 显示 RPU15 可在金黄色葡萄球菌的细胞膜上形成孔,在 R-噬菌体处理过的金黄色葡萄球菌平板上可观察到噬菌体样斑。金黄色葡萄球菌和单核细胞增生李斯特菌的 LTA 可中和 R-噬菌体的活性。铜绿假单胞菌 PU15 产生约 428 个不可诱导的 R-噬菌体颗粒。RPU15 鞘和管蛋白亚单位的分子量分别为 38 和 23 kDa。RPU15 对金黄色葡萄球菌、单核细胞增生李斯特菌、蜡状芽孢杆菌和白色念珠菌具有活性,并降低了测试的 AMR 菌株的生物膜生物量。
由于 R-噬菌体对测试细菌生物膜的有效性,本研究结果显示其具有潜在的治疗用途。
这是首次研究 R-噬菌体对金黄色葡萄球菌的抗菌和抗生物膜活性。R-噬菌体显示出噬菌体样斑的新现象。我们的发现代表了一种针对耐甲氧西林金黄色葡萄球菌和万古霉素金黄色葡萄球菌的新型治疗药物。