Peela Sreeram Chandra Murthy, Sistla Sujatha, Tamilarasu Kadhiravan, Krishnamurthy Sriram, Adhishivam B
Department of Microbiology, Jawaharlal Institute of Postgraduate Medical Education and Research, Puducherry, India.
Department of Medicine, Jawaharlal Institute of Postgraduate Medical Education and Research, Puducherry, India.
Indian J Med Microbiol. 2018 Oct-Dec;36(4):504-507. doi: 10.4103/ijmm.IJMM_18_274.
The pneumococcal iron acquisition (piaA) gene is found to be highly specific and hence proposed as a diagnostic marker for identification of pneumococci. The objective of the present study was to evaluate the piaA gene as a genetic marker for the identification of pneumococci.
Twenty isolates were initially sequenced for lytA gene using published primers. PiaA-PCR (piaA polymerase chain reaction) was performed using in-house primers and protocol. Based on the sensitivity and specificity results, a final sample of 30 pneumococcal isolates and 11 non-pneumococcal isolates confirmed with lytA- sequencing were selected. Statistical analyses were performed using OpenEpi v3.01 and GraphPad Quickcalc at P < 0.05 as the level of statistical significance.
Of the initial 20 samples tested, piaA PCR was positive in only 71.43% (10/14) of the pneumococcal isolates but was 100% specific (0/6 non-pneumococcal isolates) P = 0.011. When the PCR was performed on 41 samples, the sensitivity increased to 73.33% (95% of confidence interval [CI] = 55.55-85.82) and specificity remained the same P < 0.001. The level of agreement between the PCR and lytA-sequencing was found to be moderate (κ = 0.694; 95% CI = 0.432-0.955).
PiaA-PCR can be used as a specific marker for the identification of pneumococcus, though it is less sensitive. As the level of agreement was moderate, further analyses on a large number of samples can give conclusive evidence for its use as a diagnostic marker for pneumococcus.
发现肺炎球菌铁摄取(piaA)基因具有高度特异性,因此提议将其作为鉴定肺炎球菌的诊断标志物。本研究的目的是评估piaA基因作为鉴定肺炎球菌的遗传标志物。
最初使用已发表的引物对20株分离株进行lytA基因测序。使用内部引物和方案进行PiaA-PCR(piaA聚合酶链反应)。根据敏感性和特异性结果,选择了30株经lytA测序确认的肺炎球菌分离株和11株非肺炎球菌分离株作为最终样本。使用OpenEpi v3.01和GraphPad Quickcalc进行统计分析,以P < 0.05作为统计学显著性水平。
在最初测试的20个样本中,piaA PCR仅在71.43%(10/14)的肺炎球菌分离株中呈阳性,但特异性为100%(0/6株非肺炎球菌分离株),P = 0.011。当对41个样本进行PCR时,敏感性提高到73.33%(95%置信区间[CI] = 55.55 - 85.82),特异性保持不变,P < 0.001。发现PCR与lytA测序之间的一致性水平为中等(κ = 0.694;95% CI = 0.432 - 0.955)。
PiaA-PCR可作为鉴定肺炎球菌的特异性标志物,尽管其敏感性较低。由于一致性水平为中等,对大量样本进行进一步分析可为其作为肺炎球菌诊断标志物的应用提供确凿证据。