Prevalence, genotyping, and molecular relatedness of methicillin-resistant Staphylococcus aureus isolated from tertiary care hospitals in Jeddah, Saudi Arabia.

IF 1.5 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Turki M Dawoud, Yasser A Al-Hajjaj, Ayman Mubarak, Ayman Elbehiry, Mohamed El-Tayeb, Ihab Mohamed Moussa
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引用次数: 0

Abstract

Methicillin-resistant Staphylococcus aureus (MRSA) is a major nosocomial pathogen causing severe morbidity and mortality in hospitals globally.Transmission of MRSA occurs within the healthcare sector as a nosocomial infection, primarily facilitated by healthcare workers or patients admitted to medical facilities. The objective of this study was to evaluate the genetic characterization and similarity of MRSA strains isolated from both inpatients and outpatients who visited various healthcare facilities in Jeddah, Saudi Arabia. A total of 200 MRSA strains were isolated from participants between March 2018 and June 2019. The recovered strains were characterized using both phenotypic and genotypic methods. All isolates (n=200) tested positive for the S. aureus 16S rRNA gene, with 92.5% also testing positive for the mecA gene, while 7.5% were identified as methicillin-susceptible. Furthermore, the typing and subtyping of the staphylococcal cassette chromosome mec (SCCmec) genetic element indicated that 61.6% of the MRSA strains were classified as type III (hospital-acquired), while 32.4% were identified as type IV and 6% remained of an unknown type. Subtyping of SCCmec type IV and the detection of the Panton-Valentine leukocidin (PVL) gene were also conducted. The genetic relatedness among MRSA isolates, assessed through Random Amplified Polymorphic DNA Polymerase Chain Reaction (RAPD-PCR), revealed two primary clusters, with no discernible differentiation between outpatient and inpatient strains. Additionally, Pulsed-Field Gel Electrophoresis (PFGE) fingerprinting of the examined strains identified four major clusters. The first cluster comprised three groups (16 strains), isolated from patients with respiratory and soft tissue infections. The second cluster included two groups (12 strains), all recovered from patients with respiratory, soft tissue, and urinary tract infections (UTIs). The third and fourth clusters each contained one group (6 strains and 5 strains, respectively), all isolated from outpatients. In conclusion, Antimicrobial susceptibility testing showed significant resistance to ceftriaxone, ampicillin, and amoxicillin-clavulanic acid, with vancomycin and gentamicin being the most susceptible. Multiplex PCR identified all positive MRSA strains within hours. Most isolates were SCCmec type III and type IV. The PVL gene was found in all S. aureus isolates, especially in type IV and methicillin-sensitive strains, but not in type III. RAPD-PCR analysis revealed distinct profiles for outpatient and inpatient strains.

沙特阿拉伯吉达三级医院分离的耐甲氧西林金黄色葡萄球菌的流行、基因分型和分子相关性
耐甲氧西林金黄色葡萄球菌(MRSA)是导致全球医院严重发病率和死亡率的主要医院病原体。耐甲氧西林金黄色葡萄球菌的传播以医院感染的形式发生在卫生保健部门,主要由卫生保健工作者或入住医疗机构的患者促成。本研究的目的是评估从沙特阿拉伯吉达不同医疗机构的住院和门诊患者中分离的MRSA菌株的遗传特征和相似性。2018年3月至2019年6月期间,从参与者身上共分离出200株MRSA菌株。采用表型和基因型方法对回收的菌株进行鉴定。所有分离株(n=200)均检测出金黄色葡萄球菌16S rRNA基因阳性,其中92.5%的菌株检测出mecA基因阳性,7.5%的菌株对甲氧西林敏感。此外,葡萄球菌盒式染色体mec (SCCmec)遗传元件分型和亚分型表明,61.6%的MRSA菌株为III型(医院获得),32.4%为IV型,6%为未知型。同时进行SCCmec IV型亚型分型和Panton-Valentine leukocidin (PVL)基因检测。通过随机扩增多态DNA聚合酶链反应(RAPD-PCR)评估MRSA分离株的遗传相关性,发现两个主要集群,门诊和住院菌株之间没有明显的差异。此外,检测菌株的脉冲场凝胶电泳(PFGE)指纹图谱鉴定出4个主要集群。第一个聚类包括三组(16株),从呼吸道和软组织感染患者中分离出来。第二聚类包括两组(12株),均为呼吸道、软组织和尿路感染(uti)患者康复。第三和第四聚类各1组(分别为6株和5株),均来自门诊患者。综上所述,药敏试验显示对头孢曲松、氨苄西林、阿莫西林-克拉维酸均有明显耐药,其中万古霉素和庆大霉素最敏感。多重PCR在数小时内鉴定出所有阳性MRSA菌株。大多数分离株为SCCmec III型和IV型。PVL基因在所有金黄色葡萄球菌分离株中均存在,特别是在IV型和甲氧西林敏感株中,但在III型中未发现。RAPD-PCR分析显示门诊和住院菌株有明显差异。
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来源期刊
Cellular and molecular biology
Cellular and molecular biology 生物-生化与分子生物学
CiteScore
1.60
自引率
12.50%
发文量
331
期刊介绍: Cellular and Molecular Biology publishes original articles, reviews, short communications, methods, meta-analysis notes, letters to editor and comments in the interdisciplinary science of Cellular and Molecular Biology linking and integrating molecular biology, biophysics, biochemistry, enzymology, physiology and biotechnology in a dynamic cell and tissue biology environment, applied to human, animals, plants tissues as well to microbial and viral cells. The journal Cellular and Molecular Biology is therefore open to intense interdisciplinary exchanges in medical, dental, veterinary, pharmacological, botanical and biological researches for the demonstration of these multiple links.
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