Department of Medical Microbiology, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Serdang, Selangor, 43400 UPM, Malaysia.
Department of Microbiology and Immunology, Pathology Division, School of Medicine, International Medical University, Kuala Lumpur, Selangor, 57000, Malaysia.
Probiotics Antimicrob Proteins. 2023 Dec;15(6):1681-1699. doi: 10.1007/s12602-023-10050-0. Epub 2023 Mar 7.
Vaginal dysbiosis advocates burgeoning of devious human vaginal pathobionts like Candida species that possess multiple virulence properties and metabolic flexibility to cause infections. Inevitably, antifungal resistance may emerge due to their innate nature (e.g., biofilm formation), which assists in their virulence as well as the formation of persister cells after dispersal. In consequence, the phenomenon of biofilm involvement in vulvovaginal candidiasis (VVC) and its recurrence is becoming paramount. Lactic acid bacteria and their derivatives have proven to be hostile to Candida species. Here, we throw more light on the potency of the derivatives, i.e., cell-free supernatant (CFS) produced by an indigenously isolated vaginal Lactobacillus strain, Limosilactobacillus reuteri 29A. In the present study, we investigated the antibiofilm and antagonistic effects of L. reuteri 29A CFS, against biofilms of Candida species and in murine model of vulvovaginal candidiasis. In our in vitro biofilm study, the CFS disrupted and inhibited preformed biofilms of C. albicans and C. glabrata. Scanning electron microscopy displayed the destruction of preformed biofilms and impediment of C. albicans morphogenesis by the CFS. Gas chromatography-mass spectrometry analysis showed multiple key compounds that may act singly or synergistically. In vivo, the CFS showed no collateral damage to uninfected mice; the integrity of infected vaginal tissues was restored by the administration of the CFS as seen from the cytological, histopathological, and electron microscopical analyses. The results of this study document the potential use of CFS as an adjuvant or prophylactic option in addressing vaginal fungal infections.
阴道微生态失调提倡多种致病性病原体(如念珠菌属)的出现,这些病原体具有多种毒力特性和代谢灵活性,可导致感染。由于其固有特性(例如生物膜形成),不可避免地会出现抗真菌耐药性,这有助于它们的毒力以及在分散后形成持久性细胞。因此,生物膜参与外阴阴道念珠菌病(VVC)及其复发的现象变得至关重要。乳酸菌及其衍生物已被证明对念珠菌属具有拮抗作用。在这里,我们进一步研究了衍生产品的功效,即,由本土分离的阴道乳杆菌菌株罗伊氏乳杆菌 29A 产生的无细胞上清液(CFS)。在本研究中,我们研究了 L. reuteri 29A CFS 的抗生物膜和拮抗作用,针对念珠菌属生物膜和外阴阴道念珠菌病的小鼠模型。在我们的体外生物膜研究中,CFS 破坏并抑制了 C. albicans 和 C. glabrata 的预形成生物膜。扫描电子显微镜显示 CFS 破坏了预形成的生物膜并阻碍了 C. albicans 的形态发生。气相色谱-质谱分析显示多种可能单独或协同作用的关键化合物。在体内,CFS 对未感染的小鼠没有造成附带损害;通过给予 CFS,感染阴道组织的完整性得到了恢复,从细胞学、组织病理学和电子显微镜分析中可以看出。这项研究的结果证明了 CFS 作为辅助或预防阴道真菌感染的潜在用途。