Cracking the antigenic code of mycobacteria: CFP-10/ESAT-6 tuberculosis skin test and misleading results

IF 1.9 Q3 INFECTIOUS DISEASES
Igor Krasilnikov , Tatiana Lehnherr-Ilyina , Milana Djonovic , Irena Artamonova , Mikhail Nikitin , Nikolay Kislichkin
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Abstract

There are different tuberculosis diagnostic tools available that detect an antigen-specific immune response. The present study aims to evaluate the potential of cross-reactive responses of a CFP-10 and ESAT-6 antigen-based TB test using bioinformatics tools. The study found that the presence of the sequences coding for the CFP-10 and ESAT-6 antigens in mycobacterial genomes is not associated with their pathogenicity, and not even consistent within a single species among its strains, which can lead to either false positive or false negative test results. The data that was analyzed included genome assemblies of all available mycobacterial strains obtained from the NCBI Genome database, while the standalone BLAST and tblastn programs were utilized to detect the presence of the CFP-10 and ESAT-6 sequences. The findings revealed that a number of non-pathogenic mycobacteria contained the aforementioned sequences, while some pathogenic mycobacteria did not, indicating that a standard tuberculin skin test should be more preferable for detecting various pathogenic mycobacteria compared to antigen-specific tests. In the Mycobacterium tuberculosis complex (MTBC), the proportion of positive strains varied within individual species, indicating a complex relationship. Among non-tuberculous mycobacteria (NTMB), more than half of the analyzed species did not contain these sequences which is consistent with their non-pathogenicity. Further research is necessary to fully comprehend the relationship between MTBC pathogenicity and the CFP-10 and ESAT-6 sequences. This could lead to a conclusion that a standard tuberculin skin test, although non-specific due to the undefined antigen content, may be able to detect various pathogenic mycobacteria in a more reliable manner than antigen-specific tests.

破解分枝杆菌的抗原密码:CFP-10/ESAT-6 结核病皮试和误导性结果
目前有不同的结核病诊断工具可以检测抗原特异性免疫反应。本研究旨在利用生物信息学工具,评估基于 CFP-10 和 ESAT-6 抗原的结核病检验产生交叉反应的可能性。研究发现,CFP-10 和 ESAT-6 抗原编码序列在分枝杆菌基因组中的存在与其致病性无关,甚至在单一物种的菌株中也不一致,这可能导致假阳性或假阴性的检测结果。分析的数据包括从 NCBI 基因组数据库中获得的所有可用分枝杆菌菌株的基因组组装,同时利用独立的 BLAST 和 tblastn 程序检测 CFP-10 和 ESAT-6 序列的存在。研究结果表明,一些非致病分枝杆菌含有上述序列,而一些致病分枝杆菌则没有,这表明与抗原特异性试验相比,标准结核菌素皮肤试验更适合检测各种致病分枝杆菌。在结核分枝杆菌复合体(MTBC)中,阳性菌株的比例在不同菌种中各不相同,表明其中存在复杂的关系。在非结核分枝杆菌(NTMB)中,一半以上的分析菌种不包含这些序列,这与它们的非致病性是一致的。要充分理解 MTBC 致病性与 CFP-10 和 ESAT-6 序列之间的关系,还需要进一步的研究。由此可以得出结论,标准结核菌素皮肤试验虽然由于抗原含量不确定而不具有特异性,但可能比抗原特异性试验更可靠地检测出各种致病分枝杆菌。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Clinical Tuberculosis and Other Mycobacterial Diseases
Journal of Clinical Tuberculosis and Other Mycobacterial Diseases Medicine-Pulmonary and Respiratory Medicine
CiteScore
4.00
自引率
5.00%
发文量
44
审稿时长
30 weeks
期刊介绍: Journal of Clinical Tuberculosis and Mycobacterial Diseases aims to provide a forum for clinically relevant articles on all aspects of tuberculosis and other mycobacterial infections, including (but not limited to) epidemiology, clinical investigation, transmission, diagnosis, treatment, drug-resistance and public policy, and encourages the submission of clinical studies, thematic reviews and case reports. Journal of Clinical Tuberculosis and Mycobacterial Diseases is an Open Access publication.
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