Penicillin susceptibility among Staphylococcus aureus skin and soft tissue infections at a children's hospital.

IF 3.7 2区 生物学 Q2 MICROBIOLOGY
J Chase McNeil, Lauren M Sommer, Marritta Joseph, Kristina G Hulten, Sheldon L Kaplan
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引用次数: 0

Abstract

Shortly after its introduction into clinical practice, Staphylococcus aureus isolates gained resistance to penicillin via the acquisition of β-lactamases. A number of centers have recently described an increase in the proportion of invasive methicillin-susceptible S. aureus (MSSA), which are also susceptible to penicillin (PSSA). Little data are available regarding the prevalence or impact of PSSA in skin and soft tissue infections (SSTI). Community-acquired MSSA SSTI isolates were obtained through a surveillance study at Texas Children's Hospital from January 2017 to December 2021. A total of 200 random isolates underwent PCR for blaZ β-lactamase; blaZ-negative isolates then underwent penicillin susceptibility testing using macrobroth dilution. Isolates which were blaZ negative and had a penicillin MIC ≤0.125 µg/mL were regarded as PSSA with the remainder regarded as penicillin-resistant MSSA (PR-MSSA). All PSSA underwent multilocus sequence typing. Medical records were reviewed. The median age of subjects was 4.2 years (IQR: 1.6-10.5). PSSA accounted for 9% of isolates during the study period. PSSA and PR-MSSA cases were similar with respect to age, demographics, and rates of prior antibiotic exposure. PSSA isolates less often had vancomycin MIC ≥1.5 µg/mL. Furthermore, 39% of PSSA were variants of sequence type 1. In multivariable analyses, penicillin susceptibility was independently associated with both hospital admission and surgical intervention. PSSA account for a small but significant proportion of MSSA SSTI in children. Clinically distinguishing patients with PSSA and PR-MSSA SSTI is challenging. However, PSSA SSTI were independently associated with higher rates of hospital admission as well as the need for surgical intervention suggesting a significant clinical impact.IMPORTANCEThe vast majority of Staphylococcus aureus in the US are penicillin resistant with most clinical labs no longer reporting penicillin susceptibility for this organism. A number of centers, however, have reported increasing penicillin susceptibility among invasive S. aureus infections. Skin and soft tissue infections (SSTI) are far more common than invasive infections, yet the frequency and impact of penicillin-susceptible S. aureus (PSSA) in this population are uncertain. Through active surveillance at a children's hospital, we found that 9% of methicillin-susceptible S. aureus SSTI isolates were PSSA. PSSA were independently associated with hospital admission for the management of SSTI as well as the need for debridement in the operating room. Given that most SSTI are managed in the outpatient setting, these findings suggest a clinical impact of this phenotype and the need for a reassessment of the value in susceptibility testing and potentially even treatment with penicillin.

一家儿童医院的金黄色葡萄球菌皮肤和软组织感染病例对青霉素的敏感性。
在青霉素被引入临床实践后不久,金黄色葡萄球菌分离株通过获得β-内酰胺酶而对青霉素产生耐药性。最近,一些研究中心描述了侵袭性甲氧西林敏感金黄色葡萄球菌(MSSA)比例的增加,这些金黄色葡萄球菌也对青霉素敏感(PSSA)。关于 PSSA 在皮肤和软组织感染 (SSTI) 中的流行情况或影响,目前几乎没有相关数据。2017 年 1 月至 2021 年 12 月期间,德克萨斯儿童医院通过一项监测研究获得了社区获得性 MSSA SSTI 分离物。共对 200 例随机分离株进行了 blaZ β-内酰胺酶 PCR 检测;blaZ 阴性分离株随后使用大溪地稀释法进行了青霉素药敏试验。blaZ 阴性且青霉素 MIC ≤0.125 µg/mL 的分离物被视为 PSSA,其余则被视为耐青霉素 MSSA(PR-MSSA)。所有 PSSA 均进行了多焦点序列分型。对医疗记录进行了审查。受试者的中位年龄为 4.2 岁(IQR:1.6-10.5)。在研究期间,PSSA 占分离菌株的 9%。PSSA和PR-MSSA病例在年龄、人口统计学和既往抗生素暴露率方面相似。万古霉素 MIC ≥1.5 µg/mL 的 PSSA 分离物较少。此外,39% 的 PSSA 是序列 1 型的变种。在多变量分析中,青霉素敏感性与入院和手术干预都有独立关联。在儿童 MSSA SSTI 中,PSSA 所占比例虽小,但却很重要。在临床上区分 PSSA 和 PR-MSSA SSTI 患者具有挑战性。然而,PSSA SSTI 与较高的入院率和手术干预需求独立相关,这表明其具有重大的临床影响。重要意义美国绝大多数金黄色葡萄球菌对青霉素耐药,大多数临床实验室不再报告该菌对青霉素的敏感性。然而,一些中心报告称,侵入性金黄色葡萄球菌感染对青霉素的敏感性在增加。皮肤和软组织感染(SSTI)远比侵袭性感染更为常见,但青霉素敏感金黄色葡萄球菌(PSSA)在这一人群中的发生频率和影响尚不确定。通过对一家儿童医院进行主动监测,我们发现 9% 的甲氧西林敏感金黄色葡萄球菌 SSTI 分离物是 PSSA。PSSA 与入院治疗 SSTI 以及需要在手术室进行清创术密切相关。鉴于大多数 SSTI 都是在门诊环境中处理的,这些研究结果表明这种表型会对临床产生影响,需要重新评估药敏试验的价值,甚至可能需要使用青霉素进行治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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