在孟加拉国流通的纸币中的细菌分离物中发现了具有I176F突变的CTX-M-127
Md Zannat Ali1, Sankaranarayanan Srinivasan2, Selina Akter3
1Department of Microbiology, Jashore University of Science and Technology, Jashore, Bangladesh.
Scientific reports
|March 12, 2024
概括
多种药物耐药性,特别是扩展光谱β-乳糖酶 (ESBL) 生产细菌,可以通过纸币传播. 在孟加拉国纸币上发现的CTX-M突变可能导致梅西林纳姆耐药性.
科学领域:
- 微生物学 微生物学
- 分子生物学分子生物学
- 药物耐药性 药物耐药性 药物耐药性
背景情况:
- 扩展光谱β-乳糖酶 (ESBL) 生产生物体是挑战性感染的重要原因.
- 酶的CTX-M家族是一个快速增长的,在全球分布的群体,在Enterobacteriaceae中发现.
- 由于经常流通,纸币是传播多药耐药性的潜在载体.
研究的目的:
- 在孟加拉国纸币上选ESBL携带的细菌.
- 为了识别和描述这些纸币上存在的CTX-M突变.
- 调查这些突变对抗生素耐药性的潜在影响,特别是对美西林的抗生素耐药性.
主要方法:
- 从纸币上选携带ESBL的细菌.
- CTX-M 基因的基因测序.
- 使用瑞士模型对CTX-M变体的同质模型建模.
- 使用Autodock 4.2与野生类型和突变的CTX-M模型进行分子对接.
- 使用PyMOL进行分子相互作用的视觉检查.
主要成果:
- 部分测序的blaCTX-M基因与blaCTX-M-10和blaCTX-M-15有关.
- 已识别的单核酸替代突变:G613T (静音),A626T (I176F) 和A503G (N135D). 这些突变包括:
- 同样性建模证实与模板的高度相似性;突变残留物 (Asp135,Phe176) 保持了类似的方向.
- 分子对接预测了梅西林与Lys237,Ser240和Asp135残留物的结合,最低的结合能量在Asp135.5.
结论:
- 在孟加拉国纸币上发现的CTX-M突变与blaCTX-M-15和blaCTX-M-10有关.
- N135D和I176F突变可能会影响梅西林胺结合.
- 这些发现支持了CTX-M突变导致梅西林胺耐药性的假设,这可能与CTX-M-15转换为CTX-M-127有关.
更多相关视频
10:35Markerless Gene Deletion by Floxed Cassette Allelic Exchange Mutagenesis in Chlamydia trachomatis
Published on: January 30, 2020
6.7K
08:58Isolation and Identification of Waterborne Antibiotic-Resistant Bacteria and Molecular Characterization of their Antibiotic Resistance Genes
Published on: March 3, 2023
6.4K
相关概念视频
Mutations in Microorganisms
1.2K
Mutations are heritable changes in an organism’s genome involving alterations in the base sequence of DNA or RNA. These changes can influence cellular processes and phenotypic traits, potentially transforming the unaltered wild type into a mutant form. Such changes, termed forward mutations, are pivotal in shaping the genetic diversity of organisms.RNA viruses exhibit the highest mutation rates due to the absence of robust proofreading mechanisms during genome replication. In contrast,...
1.2K
Clinical Significance of Antibiotic Resistance
90
Methicillin-resistant Staphylococcus aureus (MRSA) presents a critical public health threat, arising from its capacity to resist β-lactam antibiotics due to acquisition of the mecA gene within the staphylococcal cassette chromosome mec (SCCmec). This gene encodes penicillin-binding protein 2a (PBP2a), which impairs binding efficacy of methicillin and other β-lactams. MRSA has evolved into distinct clonal lineages impacting humans and animals alike, reinforcing its significance within...
90
