Department of Pharmaceutical Chemistry, JSS College of Pharmacy, JSS Academy of Higher Education & Research, Ooty Nilgiris, Tamil Nadu, 643001, India.
School of Life Sciences, JSS Academy of Higher Education & Research (Ooty Campus), Longwood, Road, Ooty 643001, The Nilgiris, Mysuru, Tamil Nadu, India.
Braz J Microbiol. 2023 Sep;54(3):1809-1818. doi: 10.1007/s42770-023-01028-9. Epub 2023 Jun 22.
Multidrug resistant uropathogenic Escherichia coli (MDRUPEC) significantly correlates with recurrent, complicated, and persistent urinary tract infection (UTI). The leading cause of multidrug resistance is the ability of E. coli to form biofilms. The physiological heterogeneity, genetic incontinency, and putative events in gene expression of biofilms render them resistant to antimicrobials and the host immune system. Understanding the determinants of antimicrobial resistance and its correlation with biofilm formations will, therefore, help the development of a better strategy for treating biofilm-associated UTIs. The present study reports on the in vitro detection of biofilm formation among multidrug resistant E. coli strains isolated from urine, the major cause of communal, nosocomial, and food-borne uropathogenic UTI. This is a cross-sectional study conducted in and around Ooty, Nilgiris, India. From the 869 urine samples analyzed for UTI, 29.34% were found to be caused by E. coli. Among this about 23.92% were found to be multidrug resistant. Among the multidrug resistant E. coli isolates, 36.06% of them were potent biofilm producers. E. coli biofilms (n = 22) were resistant to the antibiotics used to treat UTI, namely, amikacin, amoxicillin, ampicillin, cefepime, cefoperazone, cefotaxime, ceftriaxone, cefuroxime, cephalotin, ciprofloxacin, co-trimoxazole, gentamicin, levofloxacin, and nalidixic acid, but sensitive to imipenem and meropenem. All the biofilm producers exhibited motility and hemaggultination but none were positive for hemolysin production. The isolated E. coli biofilms were confirmed by VITEK R Compact (bioMerieux, France) and 16S rRNA gene sequencing.
多药耐药尿路致病性大肠杆菌(MDRUPEC)与复发性、复杂性和持续性尿路感染(UTI)密切相关。大肠杆菌产生多药耐药性的主要原因是其形成生物膜的能力。生物膜的生理异质性、遗传不连续性和基因表达中的假定事件使它们能够抵抗抗生素和宿主免疫系统。因此,了解抗生素耐药性的决定因素及其与生物膜形成的相关性将有助于制定更好的治疗生物膜相关 UTI 的策略。本研究报告了从尿液中分离出的多药耐药大肠杆菌菌株体外生物膜形成的检测情况,这是社区、医院和食源性尿路致病性 UTI 的主要原因。这是一项在印度尼西亚尼加拉的 Ooty 及其周边地区进行的横断面研究。在分析的 869 份 UTI 尿液样本中,有 29.34%是由大肠杆菌引起的。在这些大肠杆菌中,约有 23.92%是多药耐药菌。在多药耐药大肠杆菌分离株中,有 36.06%是强力生物膜产生菌。大肠杆菌生物膜(n=22)对用于治疗 UTI 的抗生素(如阿米卡星、阿莫西林、氨苄西林、头孢吡肟、头孢哌酮、头孢噻肟、头孢曲松、头孢唑肟、头孢呋辛、头孢噻吩、环丙沙星、复方新诺明、庆大霉素、左氧氟沙星和萘啶酸)具有耐药性,但对亚胺培南和美罗培南敏感。所有的生物膜产生菌都表现出运动性和血凝集性,但没有产生溶血素。分离的大肠杆菌生物膜通过 VITEK R Compact(生物梅里埃,法国)和 16S rRNA 基因测序得到确认。