Frank Thiemo, Wohlfarth Esther, Claus Heike, Krone Manuel, Lâm Thiên-Trí, Kresken Michael
Institute for Hygiene and Microbiology, National Reference Center for Meningococci and Haemophilus influenzae, University of Würzburg, Würzburg, Germany.
Antiinfectives Intelligence GmbH, Cologne, Germany.
JAC Antimicrob Resist. 2024 Dec 10;6(6):dlae197. doi: 10.1093/jacamr/dlae197. eCollection 2024 Dec.
(Hi) is known as a cause of invasive and non-invasive diseases. Especially ear, nose and throat (ENT) infections are common reasons for antibiotic prescriptions in outpatient settings in Germany. Therefore, antibiotic resistance surveillance is important to provide the basis of recommendations for the empirical usage of antibiotic agents.
To provide data on susceptibility rates of oral antibiotics for non-invasive clinical Hi isolates in Germany and to investigate molecular resistance patterns of β-lactams, ciprofloxacin, doxycycline and trimethoprim/sulfamethoxazole.
Isolates were collected from a sentinel network of diagnostic laboratories in a prospective multicentre prevalence study. Antibiotic susceptibility testing was done with a commercial broth microdilution kit. MICs were interpreted according to EUCAST guidelines. Resistance gene sequencing and WGS were performed to analyze molecular antibiotic resistance patterns and genetic relationships between the isolates.
In total, 215 Hi isolates were collected from 23 laboratories across Germany. The highest resistance rates were found for amoxicillin ( = 30; 14%), cefuroxime ( = 40; 18.6%) and trimethoprim/sulfamethoxazole (co-trimoxazole) ( = 34; 15.8%). Resistance to amoxicillin was mainly due to ( = 29; 96.7%). PBP3 alterations were found in 39 of 40 cefuroxime-resistant isolates (97.5%). Two of the cefuroxime-resistant isolates harboured PBP3 mutation patterns that have not yet been associated with cefuroxime resistance; in one of them, a known mutation was found. One isolate showed no mutations in PBP3 or All co-trimoxazole-resistant isolates (15.8%) showed known mutations in and its promoter region. Additionally, point mutations in were identified in a subset of these isolates. The most frequent sequence types (STs) were ST57 ( = 10) and ST103 ( = 10). Genetic cluster analysis identified six clusters, but no epidemiological link could be confirmed.
Resistance to oral antibiotics in non-invasive clinical Hi isolates in Germany was generally low. Amoxicillin is estimated to cover 86% of infections involving non-invasive Hi and, therefore, is still effective for the first-line empirical treatment for ENT infections in Germany. Further surveillance of antimicrobial susceptibility in non-invasive Hi isolates is important to ensure the data basis for guidelines of antibiotic usage.
流感嗜血杆菌(Hi)是侵袭性和非侵袭性疾病的病因之一。尤其是耳鼻喉(ENT)感染是德国门诊抗生素处方的常见原因。因此,抗生素耐药性监测对于为抗生素的经验性使用提供建议依据至关重要。
提供德国非侵袭性临床Hi分离株对口服抗生素的药敏率数据,并研究β-内酰胺类、环丙沙星、强力霉素和甲氧苄啶/磺胺甲恶唑的分子耐药模式。
在一项前瞻性多中心患病率研究中,从诊断实验室的哨点网络收集分离株。使用商业肉汤微量稀释试剂盒进行抗生素敏感性测试。根据欧盟CAST指南解释最低抑菌浓度(MIC)。进行耐药基因测序和全基因组测序(WGS)以分析分子抗生素耐药模式以及分离株之间的遗传关系。
总共从德国各地的23个实验室收集了215株Hi分离株。阿莫西林(=30;14%)、头孢呋辛(=40;18.6%)和甲氧苄啶/磺胺甲恶唑(复方新诺明)(=34;15.8%)的耐药率最高。对阿莫西林的耐药主要是由于(=29;96.7%)。在40株头孢呋辛耐药分离株中的39株(97.5%)发现了青霉素结合蛋白3(PBP3)改变。两株头孢呋辛耐药分离株具有尚未与头孢呋辛耐药相关的PBP3突变模式;其中一株发现了已知的突变。一株分离株在PBP3或中未显示突变。所有复方新诺明耐药分离株(15.8%)在及其启动子区域显示已知突变。此外,在这些分离株的一个亚组中鉴定出中的点突变。最常见的序列类型(STs)是ST57(=10)和ST103(=10)。遗传聚类分析确定了六个聚类,但无法确认流行病学联系。
德国非侵袭性临床Hi分离株对口服抗生素的耐药性总体较低。据估计,阿莫西林可覆盖86%的非侵袭性Hi感染,因此,它对德国耳鼻喉感染的一线经验性治疗仍然有效。对非侵袭性Hi分离株的抗菌药物敏感性进行进一步监测对于确保抗生素使用指南的数据基础很重要。