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L421P突变在青霉素结合蛋白1(PBP1)中在[具体物种]染色体介导的青霉素耐药性演变中的作用。 (注:原文句末不完整,缺少具体物种信息)

The role of the L421P mutation in Penicillin-Binding Protein 1 (PBP1) in the evolution of chromosomally mediated penicillin resistance in .

作者信息

Gentile Gabriella, Guzman Bryan, Le Van Adriana, Jerse Ann E, Grad Yonatan H, Dominguez Daniel, Mortimer Tatum D, Nicholas Robert A

出版信息

bioRxiv. 2025 Jul 2:2025.06.27.662027. doi: 10.1101/2025.06.27.662027.

Abstract

UNLABELLED

encodes a mutated variant of penicillin-binding protein 1 (PBP1) and is a key resistance determinant that increases the penicillin MIC (MIC ) above the clinical breakpoint in . Despite the removal of penicillin from treatment guidelines for gonococcal infections in the 1980s, is present in nearly 50% of current isolates in the PubMLST database. Bioinformatic analysis indicates that is exclusive to isolates, whereas Leu-421 is 100% conserved in other species. To understand the involvement of in antibiotic resistance, we introduced variants encoding 16 different amino acids at position-421 into FA6140, a penicillin-resistant gonococcal isolate that naturally harbors . Proline-421 was the only mutation that increased the MIC to the same level as FA6140. We also assessed the fitness of strains with the 16 mutant alleles over multiple serial passages, both with and without sub-MIC levels of penicillin. There was no fitness defect attributed to under these experimental conditions; instead, our analyses suggest that the widespread occurrence of is driven by its capacity to increase the MIC above the clinical breakpoint. In FA6140 transformed with the mosaic allele from strain H041, a ceftriaxone-resistant isolate, increased the MIC of ceftriaxone, suggesting that ceftriaxone targets PBP1 in this strain. We conclude that the allele emerged in gonococcal isolates, increasing the MIC above the clinical breakpoint, and has remained in the population even after the removal of penicillin from treatment guidelines.

IMPORTANCE

The emergence of antibiotic-resistant threatens effective treatment of gonorrhea, one of the most common sexually transmitted infections worldwide. Understanding the genetic changes that drive and maintain resistance is crucial for anticipating future resistance trends. Here, we investigated the impact of a key resistance mutation in PBP1 (encoded by ). Although penicillin has not been used to treat gonorrhea for decades, this mutation remains widespread even in recent isolates. confers clinically relevant penicillin resistance without imposing an fitness cost. also increases resistance to ceftriaxone in strains with alleles that are associated with ceftriaxone resistance. This work highlights the role of the allele in shaping the current antibiotic resistance landscape and supports the need for ongoing surveillance and evolutionary studies of such mutations in the gonococcal population.

摘要

未标记

编码青霉素结合蛋白1(PBP1)的一种突变变体,是一个关键的耐药决定因素,可使淋病奈瑟菌的青霉素最低抑菌浓度(MIC)升高至临床断点以上。尽管在20世纪80年代青霉素已从淋病治疗指南中去除,但在PubMLST数据库中,近50%的当前淋病奈瑟菌分离株中仍存在该突变。生物信息学分析表明,该突变仅存在于淋病奈瑟菌分离株中,而亮氨酸-421在其他淋病奈瑟菌物种中100%保守。为了解该突变在抗生素耐药性中的作用,我们将编码16种不同氨基酸的该突变变体引入FA6140,这是一株天然携带该突变的耐青霉素淋病奈瑟菌分离株。脯氨酸-421是唯一能将MIC升高至与FA6140相同水平的突变。我们还评估了带有16种突变等位基因的菌株在多次连续传代过程中的适应性,传代过程中有无低于MIC水平的青霉素。在这些实验条件下,未发现该突变导致适应性缺陷;相反,我们的分析表明,该突变的广泛存在是由于其能够将MIC升高至临床断点以上。在转导了来自头孢曲松耐药分离株H041的嵌合等位基因的FA6140中,该突变增加了头孢曲松的MIC,表明头孢曲松在该菌株中靶向PBP1。我们得出结论,该等位基因在淋病奈瑟菌分离株中出现,使MIC升高至临床断点以上,并且即使在青霉素从治疗指南中去除后仍在种群中存在。

重要性

抗生素耐药淋病奈瑟菌的出现威胁到淋病的有效治疗,淋病是全球最常见的性传播感染之一。了解驱动和维持耐药性的基因变化对于预测未来的耐药趋势至关重要。在这里,我们研究了PBP1中一个关键耐药突变(由该基因编码)的影响。尽管几十年来青霉素未用于治疗淋病,但该突变甚至在最近的淋病奈瑟菌分离株中仍广泛存在。该突变赋予临床相关的青霉素耐药性,且不带来适应性代价。该突变还增加了带有与头孢曲松耐药相关等位基因的菌株对头孢曲松的耐药性。这项工作突出了该等位基因在塑造当前抗生素耐药格局中的作用,并支持对淋病奈瑟菌种群中此类突变进行持续监测和进化研究的必要性。

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