El-Banna Tarek E S, Sonbol Fatma I, Zaki Maysaa E S, Abo-Hammam Rana H
Clin Lab. 2020 Jan 1;66(1). doi: 10.7754/Clin.Lab.2019.190529.
Streptococcus pneumoniae (S. pneumoniae) is a commensal bacterium that normally colonizes the human nasopharyngeal cavity. Once disseminated, it can cause several diseases, ranging from non-invasive infections such as acute otitis media and sinusitis through to invasive infections with higher mortality. Antibiotic resistance among S. pneumoniae has increased dramatically and penicillin-resistant strains have spread worldwide with pneumococcus also being resistant to other types of antibiotics like erythromycin, tetracycline, and chloram-phenicol. The aim of the present study was to study the susceptibility of the isolated strains to β-lactam and other antibiotics from different classes and to determine the prevalence of β-lactam resistance genes among S. pneumoniae clinical isolates.
From a total of 178 sputum samples, isolates identified by standard microbiological method as S. pneu-moniae were subjected to antibiotic susceptibility tests to β-lactam and non β-lactam antimicrobial agents by disk diffusion method. Biofilm formation was detected by microtitration plate and the resistance genotype was also determined using multiplex PCR technique with primers designed for PBP genes.
Out of 178 sputum samples, sixty isolates were recovered as Streptococcus pneumoniae. Most of isolates were multidrug-resistant (MDR) possessing a high (> 0.2) multiple antibiotic resistance index (MAR) value. Biofilm formation ability of isolates were strong, moderate, weak, and none, accounting for 21.67%, 45%, 25%, and 8.33% biofilm formers, respectively, and it was found that pbp1a, pbp2b, and pbp2x were present in 33 (55%), 25 (41.7%), and 45 (75%) of isolates, respectively.
Streptococcus pneumoniae clinical isolates have an alteration in PBP resistance genes in response to β-lactam therapy which subsequently lead to increased MDR phenomena among these clinically important pathogens. These findings necessitate continuous monitoring of antimicrobial resistance to guide the empirical treatment of pneumococcal disease, as well as to encourage reflections to support public immunizations strategies.
肺炎链球菌是一种共生细菌,通常定植于人类鼻咽腔。一旦扩散,它可引发多种疾病,从非侵袭性感染如急性中耳炎和鼻窦炎到死亡率更高的侵袭性感染。肺炎链球菌的抗生素耐药性急剧增加,耐青霉素菌株已在全球传播,肺炎球菌对其他类型的抗生素如红霉素、四环素和氯霉素也具有耐药性。本研究的目的是研究分离菌株对β-内酰胺类和其他不同类别的抗生素的敏感性,并确定肺炎链球菌临床分离株中β-内酰胺耐药基因的流行情况。
从总共178份痰标本中,通过标准微生物学方法鉴定为肺炎链球菌的分离株,采用纸片扩散法对β-内酰胺类和非β-内酰胺类抗菌药物进行药敏试验。通过微量滴定板检测生物膜形成,并使用针对PBP基因设计的引物的多重PCR技术确定耐药基因型。
在178份痰标本中,有60株分离株被鉴定为肺炎链球菌。大多数分离株为多重耐药(MDR),具有较高(>0.2)的多重抗生素耐药指数(MAR)值。分离株的生物膜形成能力分别为强、中、弱和无,分别占生物膜形成者的21.67%、45%、25%和8.33%,并且发现pbp1a、pbp2b和pbp2x分别存在于33株(55%)、25株(41.7%)和45株(75%)的分离株中。
肺炎链球菌临床分离株因β-内酰胺治疗而导致PBP耐药基因发生改变,随后导致这些重要临床病原体中的多重耐药现象增加。这些发现需要持续监测抗菌药物耐药性,以指导肺炎球菌疾病的经验性治疗,并鼓励思考以支持公共免疫策略。