Pollock Nira, Dhiman Rakesh, Daifalla Nada, Farhat Maha, Campos-Neto Antonio
Boston Children's Hospital and Harvard Medical School, Boston MA, USA.
The Forsyth Institute, Cambridge MA, USA.
Microbes Infect. 2018 Apr;20(4):228-235. doi: 10.1016/j.micinf.2017.12.011. Epub 2018 Jan 3.
Identification of pathogen-specific biomarkers present in patients' serum or urine samples can be a useful diagnostic approach. In efforts to discover Mycobacterium tuberculosis (Mtb) biomarkers we identified by mass spectroscopy a unique 21-mer Mtb peptide sequence (VVLGLTVPGGVELLPGVALPR) present in the urines of TB patients from Zimbabwe. This peptide has 100% sequence homology with the protein TBCG_03312 from the C strain of Mtb (a clinical isolate identified in New York, NY, USA) and 95% sequence homology with Mtb oxidoreductase (MRGA423_21210) from the clinical isolate MTB423 (identified in Kerala, India). Alignment of the genes coding for these proteins show an insertion point mutation relative to Rv3368c of the reference H37Rv strain, which generated a unique C-terminus with no sequence homology with any other described protein. Phylogenetic analysis utilizing public sequence data shows that the insertion mutation is apparently a rare event. However, sera from TB patients from distinct geographical areas of the world (Peru, Vietnam, and South Africa) contain antibodies that recognize a purified recombinant C-terminus of the protein, thus suggesting a wider distribution of isolates that produce this protein.
鉴定患者血清或尿液样本中存在的病原体特异性生物标志物可能是一种有用的诊断方法。为了发现结核分枝杆菌(Mtb)生物标志物,我们通过质谱法在来自津巴布韦的结核病患者尿液中鉴定出一种独特的21聚体Mtb肽序列(VVLGLTVPGGVELLPGVALPR)。该肽与来自Mtb C株(在美国纽约市鉴定的临床分离株)的蛋白质TBCG_03312具有100%的序列同源性,与来自临床分离株MTB423(在印度喀拉拉邦鉴定)的Mtb氧化还原酶(MRGA423_21210)具有95%的序列同源性。编码这些蛋白质的基因比对显示,相对于参考H37Rv株的Rv3368c存在一个插入点突变,这产生了一个独特的C末端,与任何其他已描述的蛋白质没有序列同源性。利用公共序列数据进行的系统发育分析表明,插入突变显然是一个罕见事件。然而,来自世界不同地理区域(秘鲁、越南和南非)的结核病患者血清中含有识别该蛋白质纯化重组C末端的抗体,因此表明产生这种蛋白质的分离株分布更广泛。