Division of Infectious Diseases, Rush University Medical Centergrid.240684.c/Cook County Health, Chicago, Illinois, USA.
Department of Microbiology and Immunology, University of Michigan, Ann Arbor, Michigan, USA.
Microbiol Spectr. 2021 Sep 3;9(1):e0037621. doi: 10.1128/Spectrum.00376-21. Epub 2021 Jul 21.
Methicillin-resistant Staphylococcus aureus (MRSA) is a leading cause of health care-associated (HA) and community-associated (CA) infections. USA300 strains are historically CA-MRSA, while USA100 strains are HA-MRSA. Here, we update an antibiotic prediction rule to distinguish these two genotypes based on antibiotic resistance phenotype using whole-genome sequencing (WGS), a more discriminatory methodology than pulsed-field gel electrophoresis (PFGE). MRSA clinical isolates collected from 2007 to 2017 underwent WGS; associated epidemiologic data were ascertained. In developing the rule, we examined MRSA isolates that included a population with a history of incarceration. Performance characteristics of antibiotic susceptibility for predicting USA300 compared to USA100, as defined by WGS, were examined. Phylogenetic analysis was performed to examine resistant USA300 clades. We identified 275 isolates (221 USA300, 54 USA100). Combination susceptibility to clindamycin or levofloxacin performed the best overall (sensitivity 80.7%, specificity 75.9%) to identify USA300. The average number of antibiotic classes with resistance was higher for USA100 (3 versus 2, < 0.001). Resistance to ≤2 classes was predictive for USA300 (area under the curve (AUC) 0.84, 95% confidence interval 0.78 to 0.90). Phylogenetic analysis identified a cluster of USA300 strains characterized by increased resistance among incarcerated individuals. Using a combination of clindamycin or levofloxacin susceptibility, or resistance to ≤2 antibiotic classes, was predictive of USA300 as defined by WGS. Increased resistance was observed among individuals with incarceration exposure, suggesting circulation of a more resistant USA300 clade among at-risk community networks. Our phenotypic prediction rule could be used as an epidemiologic tool to describe community and nosocomial shifts in USA300 MRSA and quickly identify emergence of lineages with increased resistance. Methicillin-resistant Staphylococcus aureus (MRSA) is an important cause of health care-associated (HA) and community-associated (CA) infections, but the epidemiology of these strains (USA100 and USA300, respectively) now overlaps in health care settings. Although sequencing technology has become more available, many health care facilities still lack the capabilities to perform these analyses. In this study, we update a simple prediction rule based on antibiotic resistance phenotype with integration of whole-genome sequencing (WGS) to predict strain type based on antibiotic resistance profiles that can be used in settings without access to molecular strain typing methods. This prediction rule has many potential epidemiologic applications, such as analysis of retrospective data sets, regional monitoring, and ongoing surveillance of CA-MRSA infection trends. We demonstrate application of this rule to identify an emerging USA300 strain with increased antibiotic resistance among incarcerated individuals that deviates from the rule.
耐甲氧西林金黄色葡萄球菌(MRSA)是导致与医疗保健相关(HA)和社区相关(CA)感染的主要原因。USA300 株是历史上的 CA-MRSA,而 USA100 株是 HA-MRSA。在这里,我们更新了一种抗生素预测规则,该规则基于使用全基因组测序(WGS)对耐药表型的区分这两种基因型,这比脉冲场凝胶电泳(PFGE)更具区分性。从 2007 年至 2017 年收集了耐甲氧西林金黄色葡萄球菌临床分离株,并进行了 WGS;确定了相关的流行病学数据。在制定该规则时,我们研究了包括有监禁史人群的耐甲氧西林金黄色葡萄球菌分离株。研究了抗生素敏感性预测 USA300 与 USA100 的性能特征,USA300 和 USA100 是根据 WGS 定义的。进行了系统发育分析以检查耐药 USA300 进化枝。我们鉴定了 275 株分离株(221 株 USA300,54 株 USA100)。克林霉素或左氧氟沙星联合药敏试验总体上对识别 USA300 的效果最佳(敏感性 80.7%,特异性 75.9%)。USA100 的耐药抗生素类别平均数量(3 与 2,<0.001)更高。耐药性≤2 类可预测 USA300(曲线下面积(AUC)为 0.84,95%置信区间为 0.78 至 0.90)。系统发育分析鉴定了一个 USA300 菌株簇,该菌株簇在被监禁的个体中表现出更高的耐药性。使用克林霉素或左氧氟沙星敏感性的组合,或耐药性≤2 类抗生素,可预测 WGS 定义的 USA300。在有监禁暴露的个体中观察到耐药性增加,这表明具有更高耐药性的 USA300 进化枝在高危社区网络中传播。我们的表型预测规则可用作描述 USA300 MRSA 在社区和医院环境中变化的流行病学工具,并可快速识别具有更高耐药性的谱系的出现。耐甲氧西林金黄色葡萄球菌(MRSA)是导致与医疗保健相关(HA)和社区相关(CA)感染的重要原因,但这些菌株(分别为 USA100 和 USA300)的流行病学现在在医疗保健环境中重叠。尽管测序技术变得越来越普及,但许多医疗机构仍然缺乏执行这些分析的能力。在这项研究中,我们更新了一种简单的基于抗生素耐药表型的预测规则,该规则整合了全基因组测序(WGS),以根据抗生素耐药谱预测菌株类型,该规则可用于无法进行分子菌株分型方法的环境中。该预测规则具有许多潜在的流行病学应用,例如回顾性数据集分析,区域监测和对 CA-MRSA 感染趋势的持续监测。我们展示了该规则在识别具有更高抗生素耐药性的新兴 USA300 菌株中的应用,该菌株在被监禁的个体中出现了偏离该规则的情况。