Multiplexed real-time PCR for the detection and differentiation of Klebsiella pneumoniae O-antigen serotypes.

IF 3.7 2区 生物学 Q2 MICROBIOLOGY Microbiology spectrum Pub Date : 2024-09-03 Epub Date: 2024-08-08 DOI:10.1128/spectrum.00375-24
Damien Slater, Kian Hutt Vater, Sushmita Sridhar, Wontae Hwang, Derek Bielawski, Sarah E Turbett, Regina C LaRocque, Jason B Harris
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Abstract

Klebsiella pneumoniae has emerged as a global health threat due to its role in the spread of antimicrobial resistance and because it is a frequent cause of hospital-acquired infections and neonatal sepsis. Capsular and lipopolysaccharide (LPS) O-antigen polysaccharide surface antigens are major immunogens that are useful for strain classification and are candidates for vaccine development. We have developed real-time PCR reagents for molecular serotyping, subtyping, and quantitation of the most prevalent LPS O-antigen types (i.e., O1, O2, O3, and O5) of Klebsiella pneumoniae. We describe two applications for this O-typing assay: for screening culture isolates and for direct typing of Klebsiella pneumoniae present in stool samples. We find 100% concordance between the results of the O-typing assay and whole-genome sequencing of 81 culture isolates, and >90% agreement in O-typing performed directly on specimens of human stool, with disagreement arising primarily from a lack of sensitivity of the culture-based comparator method. Additionally, we find evidence for mixed O-type populations at varying levels of abundance in direct tests of stool from a hospitalized patient population. Taken together, these results demonstrate that this novel O-typing assay can be a useful tool for K. pneumoniae epidemiologic and vaccine studies.IMPORTANCEKlebsiella pneumoniae is an important opportunistic pathogen. The gastrointestinal (GI) tract is the primary reservoir of K. pneumoniae in humans, and GI carriage is believed to be a prerequisite for invasive infection. Knowledge about the dynamics and duration of GI carriage has been hampered by the lack of tools suitable for detection and strain discrimination. Real-time PCR is particularly suited to the higher-throughput workflows used in population-based studies, which are needed to improve our understanding of carriage dynamics and the factors influencing K. pneumoniae colonization.

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用于检测和区分肺炎克雷伯氏菌 O 抗原血清型的多重实时 PCR。
由于肺炎克雷伯菌在抗菌药耐药性传播中的作用,以及它是医院获得性感染和新生儿败血症的常见病因,肺炎克雷伯菌已成为全球健康的威胁。球囊和脂多糖(LPS)O 抗原多糖表面抗原是主要的免疫原,可用于菌株分类,也是候选的疫苗开发对象。我们开发了实时 PCR 试剂,用于对肺炎克雷伯菌最常见的 LPS O 抗原类型(即 O1、O2、O3 和 O5)进行分子血清分型、亚型和定量。我们介绍了这种 O 型分析法的两种应用:筛选培养分离物和直接对粪便样本中的肺炎克雷伯菌进行分型。我们发现,对 81 个培养分离物进行 O 型鉴定和全基因组测序的结果一致性达到 100%,而直接对人类粪便标本进行 O 型鉴定的一致性超过 90%,分歧主要来自于基于培养的比较方法缺乏灵敏度。此外,我们还发现,在对住院病人的粪便进行直接检测时,有证据表明存在不同丰度的混合 O 型群体。总之,这些结果表明,这种新型 O 型检测法可作为肺炎克雷伯菌流行病学和疫苗研究的有用工具。 重要意义 肺炎克雷伯菌是一种重要的机会性病原体。胃肠道(GI)是肺炎克雷伯菌在人类中的主要贮藏地,胃肠道带菌被认为是侵入性感染的先决条件。由于缺乏适用于检测和菌株鉴别的工具,人们对胃肠道带菌的动态和持续时间的了解受到了阻碍。实时 PCR 特别适用于基于人群的研究中使用的高通量工作流程,而这正是我们更好地了解带菌动态和影响肺炎克雷伯菌定植的因素所需要的。
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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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