Centre de recherche du CHU de Québec, Université Laval, Québec, Québec, Canada.
Département de médecine sociale et préventive, Université Laval, Québec, Québec, Canada.
PLoS One. 2019 Jul 25;14(7):e0220326. doi: 10.1371/journal.pone.0220326. eCollection 2019.
Because self-report of sexual behaviours is prone to biases, biomarkers of recent semen exposure are increasingly used to assess unprotected sex. We aimed to present a novel nested polymerase chain reaction (PCR) assay targeting testis-specific protein Y-encoded (TSPY) genes and to compare its performance in detecting recent semen exposure with that of four other assays.
Forty-five vaginal samples were selected at baseline of a prospective observational demonstration study of early antiretroviral treatment and pre-exposure prophylaxis among female sex workers in Benin. Semen exposure was assessed with: a rapid prostate-specific antigen (PSA) detection assay, a quantitative PCR targeting the sex-determining region (SRY) gene, a standard PCR targeting SRY, a standard PCR targeting TSPY, and a nested PCR targeting TSPY (n-TSPY). Because we had hypothesized that n-TSPY would be the most sensitive of the five assays while remaining specific, and as our results suggested that it was the case, sensitivity and specificity were calculated for each assay in comparison with n-TSPY.
The n-TSPY could detect male DNA at concentration 16 and 64 times lower compared to s-TSPY and s-SRY, respectively. Among the 45 vaginal samples, prevalences of semen exposure according to the different assays varied from 22.2% (95%CI: 11.2%-37.1%) to 70.5% (95%CI: 54.8%-83.2%), with the highest prevalence measured with n-TSPY. The n-TSPY products were of expected size and we observed no false-positive in female DNA controls. The assay that offered the second best performance in detecting semen exposure was the PSA rapid test, with a sensitivity of 61.3% and a specificity of 100% compared to n-TSPY.
Compared to n-TSPY, all other PCR assays had poor performance to detect semen exposure. The n-TSPY is an accessible assay that may have great utility in assessing semen exposure in studies where many factors are expected to accelerate biomarkers' clearance.
由于性行为的自我报告容易出现偏差,因此越来越多地使用精液暴露的生物标志物来评估未采取保护措施的性行为。本研究旨在提出一种新型的针对睾丸特异性蛋白 Y 编码(TSPY)基因的嵌套聚合酶链反应(PCR)检测方法,并比较其检测近期精液暴露的性能与其他四种检测方法的性能。
在贝宁开展的一项前瞻性观察性研究中,在女性性工作者中早期抗逆转录病毒治疗和暴露前预防措施的基础上,选择了 45 个阴道样本作为基线样本。使用以下方法评估精液暴露情况:快速前列腺特异性抗原(PSA)检测、性别决定区(SRY)基因定量 PCR、SRY 标准 PCR、TSPY 标准 PCR 和 TSPY 嵌套 PCR(n-TSPY)。由于我们假设 n-TSPY 将是五种检测方法中最敏感的,同时保持特异性,并且我们的结果表明情况确实如此,因此计算了每种检测方法与 n-TSPY 相比的敏感性和特异性。
与 s-TSPY 和 s-SRY 相比,n-TSPY 可以检测到浓度低 16 倍和 64 倍的男性 DNA。在 45 个阴道样本中,根据不同的检测方法,精液暴露的患病率从 22.2%(95%CI:11.2%-37.1%)到 70.5%(95%CI:54.8%-83.2%)不等,其中 n-TSPY 检测到的患病率最高。n-TSPY 产物的大小符合预期,在女性 DNA 对照中未观察到假阳性。在检测精液暴露方面表现第二好的检测方法是 PSA 快速检测,与 n-TSPY 相比,其敏感性为 61.3%,特异性为 100%。
与 n-TSPY 相比,所有其他 PCR 检测方法检测精液暴露的性能都较差。n-TSPY 是一种易于获得的检测方法,在许多因素预计会加速生物标志物清除的研究中,可能具有很大的应用价值。