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血液传播广泛耐药伤寒菌分离株中代谢蛋白表达上调。

Metabolic Proteins Expression Up-Regulated in Blood-Borne Extensively Drug-Resistant Typhi Isolates from Pakistan.

机构信息

Department of Microbiology, Kohat University of Science and Technology, Kohat 26000, Pakistan.

Department of Microbiology, Abdul Wali Khan University Mardan, Mardan 23200, Pakistan.

出版信息

Medicina (Kaunas). 2024 Aug 27;60(9):1404. doi: 10.3390/medicina60091404.

Abstract

: In the undertaken study, proteomics alterations of blood-borne XDR Typhi isolated from Pakistan were investigated using mass spectrometry. : MDR and XDR Typhi total protein lysates were fractionated, digested, and processed for nanoflow LC-LTQ- analysis. : Among the 1267 identified proteins, 37 were differentially regulated, of which 28 were up-regulated, and 9 were down-regulated in XDR Typhi as compared to MDR Typhi. Based on the functional annotation, proteins found up-regulated are involved mainly in metabolic pathways (ManA, FadB, DacC, GpmA, AphA, PfkB, TalA, FbaB, OtsA, 16504242), the biosynthesis of secondary metabolites (ManA, FadB, GlpB, GpmA, PfkB, TalA, FbaB, OtsA), microbial metabolism in diverse environments (FadB, GpmA, PfkB, NfnB, TalA, FbaB), and ABC transporters (PstS, YbeJ, MglB, RbsB, ArtJ). Proteins found down-regulated are involved mainly in carbon metabolism (FadB, GpmA, PfkB, FalA, FbaB) and the biosynthesis of amino acids (GpmA, PfkB, TalA, FbaB). Most of the identified differential proteins were predicted to be antigenic, and matched with resistome data. : A total of 28 proteins were up-regulated, and 9 were down-regulated in XDR Typhi. Further characterization of the identified proteins will help in understanding the molecular signaling involved in the emergence of XDR . Typhi.

摘要

在这项研究中,使用质谱法研究了从巴基斯坦分离出的血源性 XDR 伤寒杆菌的蛋白质组学变化。MDR 和 XDR 伤寒杆菌总蛋白裂解物经分离、消化后进行纳流 LC-LTQ-分析。在鉴定的 1267 种蛋白质中,有 37 种蛋白质差异调节,其中 28 种在 XDR 伤寒杆菌中上调,9 种下调。根据功能注释,发现上调的蛋白质主要参与代谢途径(ManA、FadB、DacC、GpmA、AphA、PfkB、TalA、FbaB、OtsA、16504242)、次生代谢物的生物合成(ManA、FadB、GlpB、GpmA、PfkB、TalA、FbaB)、不同环境中微生物的新陈代谢(FadB、GpmA、PfkB、NfnB、TalA、FbaB)和 ABC 转运蛋白(PstS、YbeJ、MglB、RbsB、ArtJ)。发现下调的蛋白质主要参与碳代谢(FadB、GpmA、PfkB、FalA、FbaB)和氨基酸的生物合成(GpmA、PfkB、TalA、FbaB)。大多数鉴定的差异蛋白被预测为抗原,与耐药组数据相匹配。XDR 伤寒杆菌中有 28 种蛋白上调,9 种蛋白下调。进一步研究鉴定出的蛋白质将有助于了解 XDR 伤寒杆菌产生过程中涉及的分子信号。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61df/11433874/308ee98512dc/medicina-60-01404-g001.jpg

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