Xinling Pan, Sujuan Zhou, Lulu Jin, Songjun Ji, Xingxing Lou, Bin Lu, Jin Zhao
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The global distribution of <i>mpt64</i> gene mutations was analyzed using MTB genome sequences from the National Center for Biotechnology Information (NCBI) database.</p><p><strong>Results: </strong>Among 821 mycobacterial specimens with negative MPT64 antigen assay results, 77 MTB strains were collected from 73 patients. Compared with MPT64-positive patients (<i>n</i> = 301), a higher percentage of MPT64-negative patients had a history of anti-tuberculosis therapy (<i>n</i> = 7, 11.1%; <i>P</i> = 0.01). Moreover, MPT64-negative patients demonstrated a lower percentage of positive Gene Xpert results than MPT64-positive patients (73.8% vs 95.1%, <i>P</i> < 0.001). Several gene mutations were detected in the MPT64-negative MTB strains, including 63 bp deletion, single nucleotide mutations, and <i>IS6110</i> insertion. Among 7,324 MTB genomes from the NCBI database, 87 strains had mutations in the <i>mpt64</i> gene sequence, with four common mutation sites causing single amino acid changes, including G34A (8.0%), A103G (27.6%), T128A (9.2%), and C477A (24.1%).</p><p><strong>Conclusion: </strong>A negative MPT64 antigen result in MTB cultures can be attributed to mutations in the <i>mpt64</i> gene, and infections caused by these strains are more likely to be misdiagnosed.</p>","PeriodicalId":12488,"journal":{"name":"Frontiers in Medicine","volume":"12 ","pages":"1531853"},"PeriodicalIF":3.1000,"publicationDate":"2025-02-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11898740/pdf/","citationCount":"0","resultStr":"{\"title\":\"<i>mpt64</i> mutations in <i>Mycobacterium tuberculosis</i> with negative MPT64 antigen assay results from a tertiary hospital in Southeastern China.\",\"authors\":\"Xinling Pan, Sujuan Zhou, Lulu Jin, Songjun Ji, Xingxing Lou, Bin Lu, Jin Zhao\",\"doi\":\"10.3389/fmed.2025.1531853\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>MPT64 protein is an effective marker for detecting <i>Mycobacterium tuberculosis</i> (MTB) in liquid culture and clinical tissue samples. However, some MTB clinical isolates test negative for this antigen because of varied mutation types across different regions.</p><p><strong>Methods: </strong>DNA samples of MPT64 antigen assay-negative MTB strains were collected from a tertiary hospital from January 2016 to January 2024, and <i>mpt64</i> gene mutations were detected by sequencing. Clinical records of patients with negative MPT64 antigen results were collected and compared with those of patients with positive results. The global distribution of <i>mpt64</i> gene mutations was analyzed using MTB genome sequences from the National Center for Biotechnology Information (NCBI) database.</p><p><strong>Results: </strong>Among 821 mycobacterial specimens with negative MPT64 antigen assay results, 77 MTB strains were collected from 73 patients. Compared with MPT64-positive patients (<i>n</i> = 301), a higher percentage of MPT64-negative patients had a history of anti-tuberculosis therapy (<i>n</i> = 7, 11.1%; <i>P</i> = 0.01). Moreover, MPT64-negative patients demonstrated a lower percentage of positive Gene Xpert results than MPT64-positive patients (73.8% vs 95.1%, <i>P</i> < 0.001). Several gene mutations were detected in the MPT64-negative MTB strains, including 63 bp deletion, single nucleotide mutations, and <i>IS6110</i> insertion. Among 7,324 MTB genomes from the NCBI database, 87 strains had mutations in the <i>mpt64</i> gene sequence, with four common mutation sites causing single amino acid changes, including G34A (8.0%), A103G (27.6%), T128A (9.2%), and C477A (24.1%).</p><p><strong>Conclusion: </strong>A negative MPT64 antigen result in MTB cultures can be attributed to mutations in the <i>mpt64</i> gene, and infections caused by these strains are more likely to be misdiagnosed.</p>\",\"PeriodicalId\":12488,\"journal\":{\"name\":\"Frontiers in Medicine\",\"volume\":\"12 \",\"pages\":\"1531853\"},\"PeriodicalIF\":3.1000,\"publicationDate\":\"2025-02-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11898740/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Frontiers in Medicine\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.3389/fmed.2025.1531853\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q1\",\"JCRName\":\"MEDICINE, GENERAL & INTERNAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in Medicine","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3389/fmed.2025.1531853","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 0
摘要
背景:MPT64蛋白是液体培养和临床组织标本中检测结核分枝杆菌(MTB)的有效标志物。然而,由于不同地区的突变类型不同,一些结核分枝杆菌临床分离株对该抗原检测呈阴性。方法:采集某三级医院2016年1月至2024年1月MPT64抗原测定阴性结核分枝杆菌DNA样本,测序检测MPT64基因突变。收集MPT64抗原阴性患者的临床记录,并与阳性患者进行比较。利用国家生物技术信息中心(NCBI)数据库中的结核分枝杆菌基因组序列分析mpt64基因突变的全球分布。结果:在73例患者的821份分枝杆菌标本中,MPT64抗原检测结果为阴性的结核分枝杆菌77株。与mpt64阳性患者(n = 301)相比,mpt64阴性患者有抗结核治疗史的比例更高(n = 7, 11.1%;P = 0.01)。此外,mpt64阴性患者的基因Xpert阳性结果比例低于mpt64阳性患者(73.8% vs 95.1%, P < 0.001)。在mpt64阴性的MTB菌株中检测到多个基因突变,包括63 bp缺失、单核苷酸突变和IS6110插入。NCBI数据库的7324株MTB基因组中,有87株存在mpt64基因序列突变,共有4个突变位点引起单氨基酸变化,分别为G34A(8.0%)、A103G(27.6%)、T128A(9.2%)和C477A(24.1%)。结论:MTB培养中MPT64抗原阴性可归因于MPT64基因突变,这些菌株引起的感染更容易被误诊。
mpt64 mutations in Mycobacterium tuberculosis with negative MPT64 antigen assay results from a tertiary hospital in Southeastern China.
Background: MPT64 protein is an effective marker for detecting Mycobacterium tuberculosis (MTB) in liquid culture and clinical tissue samples. However, some MTB clinical isolates test negative for this antigen because of varied mutation types across different regions.
Methods: DNA samples of MPT64 antigen assay-negative MTB strains were collected from a tertiary hospital from January 2016 to January 2024, and mpt64 gene mutations were detected by sequencing. Clinical records of patients with negative MPT64 antigen results were collected and compared with those of patients with positive results. The global distribution of mpt64 gene mutations was analyzed using MTB genome sequences from the National Center for Biotechnology Information (NCBI) database.
Results: Among 821 mycobacterial specimens with negative MPT64 antigen assay results, 77 MTB strains were collected from 73 patients. Compared with MPT64-positive patients (n = 301), a higher percentage of MPT64-negative patients had a history of anti-tuberculosis therapy (n = 7, 11.1%; P = 0.01). Moreover, MPT64-negative patients demonstrated a lower percentage of positive Gene Xpert results than MPT64-positive patients (73.8% vs 95.1%, P < 0.001). Several gene mutations were detected in the MPT64-negative MTB strains, including 63 bp deletion, single nucleotide mutations, and IS6110 insertion. Among 7,324 MTB genomes from the NCBI database, 87 strains had mutations in the mpt64 gene sequence, with four common mutation sites causing single amino acid changes, including G34A (8.0%), A103G (27.6%), T128A (9.2%), and C477A (24.1%).
Conclusion: A negative MPT64 antigen result in MTB cultures can be attributed to mutations in the mpt64 gene, and infections caused by these strains are more likely to be misdiagnosed.
期刊介绍:
Frontiers in Medicine publishes rigorously peer-reviewed research linking basic research to clinical practice and patient care, as well as translating scientific advances into new therapies and diagnostic tools. Led by an outstanding Editorial Board of international experts, this multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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