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对伯克霍尔德菌进行全基因组测序分析,比较耐药菌株和全敏感菌株,发现了新的耐药生物标志物。

Whole-genome sequencing analysis of Burkholderia pseudomallei comparing drug-resistant and pan-susceptible isolates reveals novel biomarkers for drug resistance.

作者信息

Hinwan Yothin, Nithimongkolchai Nut, Trisakul Kanwara, Kaewseekhao Benjawan, Wonglakorn Lumyai, Chetchotisakd Ploenchan, Chareonsudjai Sorujsiri, Sirichoat Auttawit, Nithichanon Arnone, Phelan Jody, Clark Taane G, Faksri Kiatichai

机构信息

Department of Microbiology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand; Research and Diagnostic Center for Emerging Infectious Diseases (RCEID), Khon Kaen University, Khon Kaen, Thailand.

Clinical Laboratory Section, Srinagarind Hospital, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.

出版信息

Infect Genet Evol. 2025 Sep;133:105779. doi: 10.1016/j.meegid.2025.105779. Epub 2025 Jun 5.

Abstract

Melioidosis, caused by the gram-negative bacterium Burkholderia pseudomallei (Bp), poses a significant health threat due to its potential for drug resistance, which can severely limit available treatment options. To investigate this, we conducted a comparative genomic analysis of 38 drug-resistant (DR) and 300 drug-susceptible (DS) Bp isolates to identify genetic markers associated with antimicrobial resistance. Our study identified seven significant single-nucleotide polymorphisms (SNPs) linked to drug resistance: two with ceftazidime (CAZ), and five with meropenem (MEM). Pathway analysis revealed that AMC resistance was associated with alterations in fatty-acid metabolism, whereas CAZ resistance was associated with changes in membrane protein pathways. These findings highlighted how Bp develops resistance to key antibiotics through various mechanisms. In addition, we discovered 21 novel genetic variants in known drug-resistance genes, including 15 SNPs and six short insertions or deletions (indels). These previously unreported variants could contribute to resistance, highlighting the genetic diversity and adaptability to antimicrobial pressures of Bp. These findings deepen our understanding of Bp drug resistance and offer valuable insights into genetic markers with the potential to enhance diagnostic precision. By enriching the resistance database, this work provides prospective tools for early resistance prediction, facilitating prompt and effective treatment strategies. Furthermore, it emphasizes the critical role of genetic investigations in addressing the challenge of antibiotic resistance in melioidosis.

摘要

类鼻疽病由革兰氏阴性菌伯克霍尔德菌属假鼻疽杆菌(Bp)引起,因其具有耐药性,对健康构成重大威胁,这可能会严重限制可用的治疗选择。为了对此进行研究,我们对38株耐药(DR)和300株药敏(DS)的Bp分离株进行了比较基因组分析,以确定与抗菌药物耐药性相关的遗传标记。我们的研究确定了七个与耐药性相关的重要单核苷酸多态性(SNP):两个与头孢他啶(CAZ)相关,五个与美罗培南(MEM)相关。通路分析表明,对氨曲南的耐药性与脂肪酸代谢改变有关,而对CAZ的耐药性与膜蛋白通路变化有关。这些发现突出了Bp如何通过各种机制对关键抗生素产生耐药性。此外,我们在已知的耐药基因中发现了21个新的遗传变异,包括15个SNP和6个短插入或缺失(indel)。这些先前未报道的变异可能导致耐药性,突出了Bp的遗传多样性和对抗菌压力的适应性。这些发现加深了我们对Bp耐药性的理解,并为有可能提高诊断准确性的遗传标记提供了有价值的见解。通过丰富耐药性数据库,这项工作为早期耐药性预测提供了前瞻性工具,促进了及时有效的治疗策略。此外,它强调了基因研究在应对类鼻疽病抗生素耐药性挑战中的关键作用。

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