Department of Clinical Microbiology, School of Medicine and Dentistry, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.
Laboratory Unit, Prestea Government Hospital, Prestea, Ghana.
Pan Afr Med J. 2022 Dec 27;43:207. doi: 10.11604/pamj.2022.43.207.33734. eCollection 2022.
quinolones are critically important antibiotics that are reserved for treating very severe infections caused by multidrug-resistant bacterial pathogens. However, their indiscriminate uses have resulted in an increased number of resistant strains in many parts of the world including Ghana. We determined the quinolone resistance profile of Gram-negative bacterial pathogens and characterized the underlying molecular determinants of resistance.
Gram-negative pathogens obtained from clinical specimens at three hospital laboratories were tested for resistance to quinolones and other commonly used antibiotics. ESBL production among the Enterobacterial isolates was confirmed using the combined disc diffusion method. We then used PCR to determine seven types of plasmid-mediated quinolone resistance genes present in the isolates resistant to nalidixic acid and ciprofloxacin.
in this study, 29.5% of the isolates were resistant to ciprofloxacin, with the highest of 50% among E. coli resistance to the other quinolones was levofloxacin (24.4%), norfloxacin (24.9%), and nalidixic acid (38.9%). Significant proportions of the quinolone-resistant isolates were ESBL producers (P-values < 0.001). The aac(6´)-Ib-cr, qnrS, oqxA, and qepA genes were present in 43 (89.6%), 27 (56.3%), 23 (47.9%), and one (2.1%) of the isolates, respectively. None of the isolates tested positive to qnrA, qnrB, and oqxB genes. The presence of the aac(6´)-Ib-cr gene positively correlated with resistance to ceftriaxone, cefotaxime, and gentamicin (P-values < 0.05).
high proportions of Gram-negative bacterial isolates were resistant to quinolones and most of these isolates possessed multiple PMQR genes. There is a need to implement measures to limit the spread of these organisms.
喹诺酮类药物是至关重要的抗生素,仅用于治疗由多种耐药细菌病原体引起的严重感染。然而,在包括加纳在内的世界许多地区,由于其滥用,耐药菌株的数量不断增加。我们确定了革兰氏阴性细菌病原体的喹诺酮类药物耐药谱,并对耐药的潜在分子决定因素进行了特征描述。
从三家医院实验室的临床标本中获得革兰氏阴性病原体,对其进行喹诺酮类药物和其他常用抗生素的耐药性测试。采用联合纸片扩散法确认肠杆菌属分离物中 ESBL 的产生。然后,我们使用 PCR 确定对萘啶酸和环丙沙星耐药的分离物中存在的七种类型的质粒介导的喹诺酮类药物耐药基因。
在这项研究中,29.5%的分离物对环丙沙星耐药,其中大肠杆菌对其他喹诺酮类药物的耐药率最高,为 50%,左氧氟沙星(24.4%)、诺氟沙星(24.9%)和萘啶酸(38.9%)。相当比例的喹诺酮类耐药分离物是 ESBL 产生者(P 值<0.001)。aac(6´)-Ib-cr、qnrS、oqxA 和 qepA 基因分别存在于 43 株(89.6%)、27 株(56.3%)、23 株(47.9%)和 1 株(2.1%)的分离物中。没有分离物对 qnrA、qnrB 和 oqxB 基因呈阳性。aac(6´)-Ib-cr 基因的存在与对头孢曲松、头孢噻肟和庆大霉素的耐药性呈正相关(P 值<0.05)。
革兰氏阴性细菌分离物中相当大的比例对喹诺酮类药物耐药,其中大多数分离物具有多种 PMQR 基因。需要采取措施限制这些生物体的传播。