Genetic Concordance of Staphylococcus aureus From Oropharyngeal and Sputum Cultures in People With Cystic Fibrosis.

IF 2.7 3区 医学 Q1 PEDIATRICS Pediatric Pulmonology Pub Date : 2025-01-01 DOI:10.1002/ppul.27475
Christian F Zirbes, Andries Feder, Anthony J Pamatmat, Alyssa R Bartels, Nicholas J Pitcher, Alexis L Rozen, Mary Teresi, Justin Krogh, Margaret Regan, Erin A Arnold, Jared J Hill, Lindsey D Reinhardt, Carlos L Oberto, Linda Boyken, Valérie C Reeb, Ahmed M Moustafa, Paul J Planet, Anthony J Fischer
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Abstract

Background: People with cystic fibrosis (CF) may not expectorate sputum at young ages or after they receive CFTR modulators. While oropharyngeal swabs are commonly used to test for lower airway pathogens, it is unknown whether Staphylococcus aureus from the oropharynx matches the strain(s) infecting the lungs. Our goal was to determine whether oropharyngeal and sputum isolates of S. aureus are genetically distinct in a cohort of patients with CF.

Methods: We obtained historical S. aureus isolates from patients who intermittently expectorated sputum in 2018, and we prospectively cultured S. aureus from oropharyngeal swabs and sputum from subjects with CF between August 2020 and February 2022. We performed short-read whole genome sequencing, determined sequence type, and performed phylogenetic analysis using S. aureus core genome single nucleotide polymorphisms (SNPs). We assigned isolates from a patient to the same strain if they had the same sequence type and differed by ≤ 60 SNPs or the isolates were not disturbed by clade breaker analysis.

Results: 36 subjects had S. aureus in ≥ 1 oropharyngeal swab and ≥ 1 sputum in 2018. In the prospective collection, 31 subjects had synchronous oropharyngeal swab and sputum collections. Although polyclonal infections were detected, sputum and oropharyngeal isolates of S. aureus typically matched the same strain within study subjects, both over the span of 2018 (31/36 patients) and when collected simultaneously from 2020 to 2022 (29/31 patients).

Conclusions: In patients with CF who intermittently produce sputum, oropharyngeal swabs identify S. aureus with genetic and phenotypic similarity to those cultured from sputum.

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囊性纤维化患者口咽和痰培养金黄色葡萄球菌的遗传一致性。
背景:囊性纤维化(CF)患者在年轻时或接受CFTR调节剂后可能不会咳痰。虽然口咽拭子通常用于检测下呼吸道病原体,但尚不清楚来自口咽的金黄色葡萄球菌是否与感染肺部的菌株相匹配。我们的目的是确定在一组CF患者中,口咽和痰中分离的金黄色葡萄球菌是否具有遗传差异。方法:我们从2018年间歇性咳痰的患者中获得了历史上的金黄色葡萄球菌分离株,并从2020年8月至2022年2月期间CF患者的口咽拭子和痰中前瞻性地培养了金黄色葡萄球菌。我们进行了短读全基因组测序,确定了序列类型,并利用金黄色葡萄球菌核心基因组单核苷酸多态性(SNPs)进行了系统发育分析。如果患者的分离株具有相同的序列类型,且差异≤60个snp,或者分离株没有受到进化支断裂分析的干扰,我们将其分配到同一菌株。结果:2018年有36例受试者在≥1份口咽拭子和≥1份痰液中检出金黄色葡萄球菌。在前瞻性收集中,31名受试者同时进行口咽拭子和痰液收集。尽管检测到多克隆感染,但在2018年(31/36例患者)和2020年至2022年(29/31例患者)同时收集的痰液和口咽分离物通常与研究对象中的同一菌株相匹配。结论:在间歇性产痰的CF患者中,口咽拭子鉴定出的金黄色葡萄球菌与从痰中培养的金黄色葡萄球菌具有遗传和表型相似性。
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来源期刊
Pediatric Pulmonology
Pediatric Pulmonology 医学-呼吸系统
CiteScore
6.00
自引率
12.90%
发文量
468
审稿时长
3-8 weeks
期刊介绍: Pediatric Pulmonology (PPUL) is the foremost global journal studying the respiratory system in disease and in health as it develops from intrauterine life though adolescence to adulthood. Combining explicit and informative analysis of clinical as well as basic scientific research, PPUL provides a look at the many facets of respiratory system disorders in infants and children, ranging from pathological anatomy, developmental issues, and pathophysiology to infectious disease, asthma, cystic fibrosis, and airborne toxins. Focused attention is given to the reporting of diagnostic and therapeutic methods for neonates, preschool children, and adolescents, the enduring effects of childhood respiratory diseases, and newly described infectious diseases. PPUL concentrates on subject matters of crucial interest to specialists preparing for the Pediatric Subspecialty Examinations in the United States and other countries. With its attentive coverage and extensive clinical data, this journal is a principle source for pediatricians in practice and in training and a must have for all pediatric pulmonologists.
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