Mardin Artuklu University, Vocational Higher School of Health Services, Department of Medical Services and Techniques, Mardin, Turkey.
Beykent University, Medical Faculty, Department of Medical Microbiology, Istanbul, Turkey.
Photodiagnosis Photodyn Ther. 2020 Mar;29:101584. doi: 10.1016/j.pdpdt.2019.101584. Epub 2019 Nov 2.
The purpose of this research was to examine biofilm (icaA, icaD and bap) and adhesin (clfA, fnbA, cna) genes, and also assess the genotypic and phenotypic antimicrobial resistance patterns of Staphylococcus aureus strains taken from wound specimens in Mardin, Turkey. A total of 220 wound specimens were investigated. The biofilm forming ability and resistance pattern for eleven antimicrobial agents were investigated by conventional and multiplex PCR methods. S. aureus were taken from 112 (50.9%) of 220 wound specimens. Moreover, biofilm production was found in 79 (70.5%) of the 112 S. aureus isolates. 97 (86.6%) strains of all isolates were positive for icaA and icaD, and 15 (13.4%) for bap. The adhesin genes, cna, fnbA and clfA were detected in 98 (87.5%), 87 (77.7%), and 75 (66.9%) strains, respectively. The numbers of MSSA and MRSA bearing antimicrobial resistance genes were 19 (16.96%) and 32 (28.57%) for blaZ, 9 (8.04%) and 17 (15.18%) for tetK, 6 (5.36%) and 14 (12.5%) for ermC, 2 (1.79%) and 7 (6.25%) for tetM, 0 (0%) and 5 (4.46%) for mecA, 2 (1.79%) and 4 (3.57%) for ermA, 1 (0.89%) and 2 (1.79%) for both tetK and tetM, respectively. Our findings indicate that multiplex PCR is a suitable way for identifying biofilm and adhesin producing S. aureus. Our data also provided a country-wide oversight of the S. aureus antimicrobial resistance gene profiles for the properly therapy of patients and to control the spreading of the resistance genes.
本研究旨在检测来自土耳其马尔丁的伤口标本中的金黄色葡萄球菌菌株的生物膜(icaA、icaD 和 bap)和黏附素(clfA、fnbA、cna)基因,并评估其基因型和表型抗菌药物耐药模式。共研究了 220 个伤口标本。通过常规和多重 PCR 方法检测了 11 种抗菌药物的生物膜形成能力和耐药模式。从 220 个伤口标本中分离出 112 株(50.9%)金黄色葡萄球菌。此外,在 112 株金黄色葡萄球菌分离株中发现 79 株(70.5%)可产生生物膜。所有分离株中,97 株(86.6%)为 icaA 和 icaD 阳性,15 株(13.4%)为 bap 阳性。cna、fnbA 和 clfA 黏附素基因在 98 株(87.5%)、87 株(77.7%)和 75 株(66.9%)菌株中被检测到。blaZ 耐药基因阳性的 MSSA 和 MRSA 菌株分别为 19 株(16.96%)和 32 株(28.57%),tetK 耐药基因阳性的 MSSA 和 MRSA 菌株分别为 9 株(8.04%)和 17 株(15.18%),ermC 耐药基因阳性的 MSSA 和 MRSA 菌株分别为 6 株(5.36%)和 14 株(12.5%),tetM 耐药基因阳性的 MSSA 和 MRSA 菌株分别为 2 株(1.79%)和 7 株(6.25%),mecA 耐药基因阳性的 MSSA 和 MRSA 菌株均为 0 株(0%),ermA 耐药基因阳性的 MSSA 和 MRSA 菌株分别为 2 株(1.79%)和 4 株(3.57%),tetK 和 tetM 耐药基因均阳性的 MSSA 和 MRSA 菌株分别为 1 株(0.89%)和 2 株(1.79%)。我们的研究结果表明,多重 PCR 是一种鉴定产生物膜和黏附素的金黄色葡萄球菌的合适方法。我们的数据还为全国范围内的金黄色葡萄球菌抗菌药物耐药基因谱提供了一个概况,以便为患者提供适当的治疗,并控制耐药基因的传播。