College of Medicine, Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai, United Arab Emirates.
Department of Optical Molecular Diagnostics and System Technology, Leibniz Institute of Photonic Technology (IPHT), Jena, Germany.
Front Cell Infect Microbiol. 2021 Oct 18;11:754523. doi: 10.3389/fcimb.2021.754523. eCollection 2021.
Panton Valentine leukocidin (PVL) is a virulence factor which is associated with methicillin sensitive and resistant (MSSA/MRSA) causing skin and soft tissue infections (SSTI). This study aimed to evaluate a novel lateral flow immunoassay (LFI) for PVL detection in cultures and to describe their genotypic characterization.
The study was carried out from January-August 2020 in Dubai, United Arab Emirates. isolates associated with SSTI were tested for PVL detection using LFI. DNA microarray-based assays were used for molecular characterization including detection of genes.
One-hundred thirty-five patients with a clinical diagnosis of SSTIs were recruited. Sixty-six patients received antibiotics, mostly beta lactams (n=36) and topical fusidic acid (n=15). One-hundred twenty-nine isolates (MRSA: n=43; MSSA: n=86) were tested by LFI and DNA microarrays. All 76 (58.9%) isolates which were unambiguously negative for the PVL in LFI were negative for genes using the DNA microarray. All the LFI PVL positive isolates (n=53) had genes detected. This translates into 100% each for sensitivity, specificity, positive and negative predictive values for the LFI. The LFI typically takes about 15 min inclusive of a 10 min incubation period. Predominant clonal complexes (CC) were CC30 (n=18), CC22 (n=13), CC5 (n=12), CC1 (n=11), CC152 (n=8), CC15 (n=7); CC97 (n=7); CC8 and CC20 (n=6 each). Among MRSA, the proportion of pvl-positives (35/43; 81%) was higher than among MSSA (n/N=18/86; 21%). The fusidic acid resistance gene was detected in 14 MRSA (33%) compared to 8 MSSA (9%). A co-carriage of and genes was present in 7 MRSA and in one MSSA.
LFI shows excellent diagnostic accuracy indices for rapid identification of PVL in MSSA/MRSA in a setting with high prevalence of strains. The high occurrence of and genes in MRSA strains causing SSTI is of concern and needs constant surveillance.
Panton-Valentine 白细胞毒素 (PVL) 是一种毒力因子,与耐甲氧西林金黄色葡萄球菌 (MSSA/MRSA) 引起的皮肤和软组织感染 (SSTI) 有关。本研究旨在评估一种用于检测培养物中 PVL 的新型侧向流动免疫测定 (LFI),并描述其基因特征。
该研究于 2020 年 1 月至 8 月在阿拉伯联合酋长国迪拜进行。对与 SSTI 相关的 分离株进行 LFI 检测以检测 PVL。使用 DNA 微阵列分析检测 基因进行分子特征分析。
共招募了 135 名临床诊断为 SSTIs 的患者。66 名患者接受了抗生素治疗,主要是β内酰胺类(n=36)和局部应用的夫西地酸(n=15)。129 株(MRSA:n=43;MSSA:n=86)分离株用 LFI 和 DNA 微阵列进行了检测。所有 76 株(58.9%)LFI 检测结果为阴性的分离株使用 DNA 微阵列检测 基因均为阴性。所有 53 株 LFI PVL 阳性分离株均检测到 基因。这意味着 LFI 的灵敏度、特异性、阳性和阴性预测值均为 100%。LFI 通常需要大约 15 分钟,包括 10 分钟的孵育时间。主要的克隆复合体(CC)为 CC30(n=18)、CC22(n=13)、CC5(n=12)、CC1(n=11)、CC152(n=8)、CC15(n=7);CC97(n=7);CC8 和 CC20(n=6 个)。在 MRSA 中,pvl 阳性的比例(35/43;81%)高于 MSSA(18/86;21%)。在 14 株 MRSA(33%)中检测到 fusidic 酸耐药基因 ,而在 8 株 MSSA(9%)中检测到。在 7 株 MRSA 和 1 株 MSSA 中存在 和 基因的共同携带。
LFI 显示出优异的诊断准确性指数,可快速鉴定高流行 菌株引起的 MSSA/MRSA 中的 PVL。引起 SSTI 的 MRSA 菌株中 和 基因的高发生率令人担忧,需要持续监测。