Department of Food Hygiene and Technology, Faculty of Veterinary Medicine, University of Belgrade, Belgrade, Serbia.
Eko-Lab Ltd Al Dahra, Padinska Skela, Serbia.
Curr Microbiol. 2020 Dec;77(12):4045-4052. doi: 10.1007/s00284-020-02236-4. Epub 2020 Oct 15.
Due to its ubiquity, ability to form biofilms, and acquire resistance mechanisms, Pseudomonas spp. become one of the major challenge for healthcare settings and food industry. The aims of this study were to assess the biofilm production of Pseudomonas spp. recovered from clinical and food specimens and to evaluate their antimicrobial resistance. A total of 108 isolates of Pseudomonas spp. were included in the study, 48 being clinical isolates recovered from patients admitted to four tertiary care hospitals throughout Serbia and 60 were isolated from the bulk tank milk samples and meat carcasses. Biofilm production was analyzed by microtiter plate assay. Antimicrobial susceptibility was evaluated by disk diffusion method according to the CLSI guidelines, while class A and B β-lactamases encoding genes were screened by PCR. A total of 98 (90.7%) strains were biofilm producers (moderate producer: 68, 69.4%; strong producer: 8, 8.2%). Although a slightly higher percentage of clinical isolates were biofilm producers (91.7%) compared to food isolates (90%), statistical significance was not observed (P > 0.05). The proportion of carbapenem-resistant Pseudomonas aeruginosa (CRPA) isolates was significantly higher among clinical (42%) isolates compared to food (1.7%) Pseudomonads (P < 0.05). The bla and bla genes were found in ESBL (seven isolates) and MBL (two isolates) production, respectively. In the present study, we confirmed that biofilm formation was highly present in both clinical and food Pseudomonas spp. irrespective of the prior existence of resistance genes. Additionally, clinical settings pose a major reservoir of MDR Pseudomonas spp. and especially CRPA isolates.
由于其普遍存在、形成生物膜的能力以及获得耐药机制,假单胞菌已成为医疗保健环境和食品工业的主要挑战之一。本研究旨在评估从临床和食品标本中分离的假单胞菌的生物膜形成能力,并评估其抗菌药物耐药性。本研究共纳入 108 株假单胞菌,其中 48 株为来自塞尔维亚四家三级护理医院的患者临床分离株,60 株为从储奶罐奶样和肉尸中分离的菌株。采用微量平板法分析生物膜形成能力。根据 CLSI 指南,采用纸片扩散法评估抗菌药物敏感性,同时通过 PCR 筛选 A 类和 B 类β-内酰胺酶编码基因。共有 98 株(90.7%)为生物膜形成菌(中度产膜菌:68 株,占 69.4%;强产膜菌:8 株,占 8.2%)。尽管临床分离株的生物膜形成率(91.7%)略高于食品分离株(90%),但差异无统计学意义(P>0.05)。与食品假单胞菌(1.7%)相比,临床分离的耐碳青霉烯类铜绿假单胞菌(CRPA)的比例明显更高(42%,P<0.05)。在产 ESBL 和 MBL 的菌株中分别发现了 bla 和 bla 基因。在本研究中,我们证实了生物膜形成在临床和食品假单胞菌中都高度存在,而与耐药基因的存在与否无关。此外,临床环境是 MDR 假单胞菌,特别是 CRPA 分离株的主要储存库。