首页> 美国卫生研究院文献>PLoS Neglected Tropical Diseases >Rapid Treponema pallidum Clearance from Blood and Ulcer Samples following Single Dose Benzathine Penicillin Treatment of Early Syphilis
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Rapid Treponema pallidum Clearance from Blood and Ulcer Samples following Single Dose Benzathine Penicillin Treatment of Early Syphilis

机译:单剂量苄星青霉素治疗早期梅毒后从血液和溃疡样品中快速清除梅毒螺旋体

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摘要

Currently, the efficacy of syphilis treatment is measured with anti-lipid antibody tests. These can take months to indicate cure and, as a result, syphilis treatment trials require long periods of follow-up. The causative organism, Treponema pallidum (T. pallidum), is detectable in the infectious lesions of early syphilis using DNA amplification. Bacteraemia can likewise be identified, typically in more active disease. We hypothesise that bacterial clearance from blood and ulcers will predict early the standard serology-measured treatment response and have developed a qPCR assay that could monitor this clearance directly in patients with infectious syphilis. Patients with early syphilis were given an intramuscular dose of benzathine penicillin. To investigate the appropriate sampling timeframe samples of blood and ulcer exudate were collected intensively for T. pallidum DNA (tpp047 gene) and RNA (16S rRNA) quantification. Sampling ended when two consecutive PCRs were negative. Four males were recruited. The mean peak level of T. pallidum DNA was 1626 copies/ml whole blood and the mean clearance half-life was 5.7 hours (std. dev. 0.53). The mean peak of 16S rRNA was 8879 copies/ml whole blood with a clearance half-life of 3.9 hours (std. dev. 0.84). From an ulcer, pre-treatment, 67,400 T. pallidum DNA copies and 7.08x107 16S rRNA copies were detected per absorbance strip and the clearance half-lives were 3.2 and 4.1 hours, respectively. Overall, T. pallidum nucleic acids were not detected in any sample collected more than 56 hours (range 20–56) after treatment. All patients achieved serologic cure. In patients with active early syphilis, measuring T. pallidum levels in blood and ulcer exudate may be a useful measure of treatment success in therapeutic trials. These laboratory findings need confirmation on a larger scale and in patients receiving different therapies.
机译:目前,梅毒治疗的功效通过抗脂质抗体测试来衡量。这些可能需要几个月的时间才能表明治愈,因此,梅毒治疗试验需要长期的随访。使用DNA扩增可在早期梅毒的感染性病变中检出致病性生物梅毒螺旋体(T. pallidum)。同样,通常在活动性较强的疾病中也可以鉴定细菌血症。我们假设血液和溃疡中的细菌清除率将在早期预测标准的血清学测量的治疗反应,并开发了可以直接在感染性梅毒患者中监测此清除率的qPCR分析方法。梅毒早期的患者给予肌内注射苄星青霉素。为了研究适当的采样时间框架,集中收集血液和溃疡渗出液样品,以进行苍白锥DNA DNA(tpp047基因)和RNA(16S rRNA)定量。当两个连续PCR均为阴性时,采样结束。招募了四名男性。苍白螺旋体DNA的平均峰值水平为1626拷贝/ ml全血,平均清除半衰期为5.7小时(标准偏差0.53)。 16S rRNA的平均峰为8879拷贝/ ml全血,清除半衰期为3.9小时(标准偏差0.84)。从溃疡处进行预处理,每个吸光带检测出67,400个苍白螺旋体DNA拷贝和7.08x107 16S rRNA拷贝,清除半衰期分别为3.2小时和4.1小时。总体而言,治疗后超过56小时(范围20-56)收集的任何样品中均未检测到苍白螺旋体核酸。所有患者均达到血清学治愈。在患有早期梅毒的患者中,测量血液中的梅毒螺旋体水平和溃疡渗出液可能是治疗试验中治疗成功的有用指标。这些实验室发现需要在更大范围内以及接受不同疗法的患者中得到确认。

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