Department of Biology, Faculty of Medicine, Masaryk University, Brno, Czech Republic.
National Department of Health, Aopi Centre, Port Moresby, Papua New Guinea.
PLoS Negl Trop Dis. 2024 Jan 2;18(1):e0011831. doi: 10.1371/journal.pntd.0011831. eCollection 2024 Jan.
Yaws is an endemic disease caused by Treponema pallidum subsp. pertenue (TPE) that primarily affects children in rural regions of the tropics. The endemic character of yaws infections and the expected exclusive reservoir of TPE in humans opened a new opportunity to start a yaws eradication campaign. We have developed a multi-locus sequence typing (MLST) scheme for TPE isolates combining the previously published (TP0548, TP0488) and new (TP0858) chromosomal loci, and we compared this typing scheme to the two previously published MLST schemes. We applied this scheme to TPE-containing clinical isolates obtained during a mass drug administration study performed in the Namatanai District of Papua New Guinea between June 2018 and December 2019. Of 1081 samples collected, 302 (28.5%) tested positive for TPE DNA, from which 255 (84.4%) were fully typed. The TPE PCR-positivity in swab samples was higher in younger patients, patients with single ulcers, first ulcer episodes, and with ulcer duration less than six months. Non-treponemal serological test positivity correlated better with PCR positivity compared to treponema-specific serological tests. The MLST revealed a low level of genetic diversity among infecting TPE isolates, represented by just three distinct genotypes (JE11, SE22, and TE13). Two previously used typing schemes revealed similar typing resolutions. Two new alleles (one in TP0858 and one in TP0136) were shown to arise by intragenomic recombination/deletion events. Compared to samples genotyped as JE11, the minor genotypes (TE13 and SE22) were more frequently detected in samples from patients with two or more ulcers and patients with higher values of specific TP serological tests. Moreover, the A2058G mutation in the 23S rRNA genes of three JE11 isolates was found, resulting in azithromycin resistance.
雅司病是由苍白密螺旋体亚种(TPE)引起的地方性疾病,主要影响热带农村地区的儿童。雅司病感染的地方性特征和 TPE 在人类中唯一预期的储主为开展雅司病根除运动提供了新的机会。我们结合先前发表的(TP0548、TP0488)和新的(TP0858)染色体基因座,开发了一种用于 TPE 分离株的多位点序列分型(MLST)方案,并将该分型方案与之前发表的两种 MLST 方案进行了比较。我们将该方案应用于 2018 年 6 月至 2019 年 12 月期间在巴布亚新几内亚纳马塔奈区进行的一次大规模药物治疗研究中获得的含 TPE 的临床分离株。在采集的 1081 个样本中,有 302 个(28.5%)TPE DNA 检测呈阳性,其中 255 个(84.4%)完全定型。在较年轻的患者、有单个溃疡的患者、首次出现溃疡的患者和溃疡持续时间少于 6 个月的患者中,拭子样本中 TPE PCR 阳性率更高。非梅毒血清学检测阳性与梅毒螺旋体特异性血清学检测相比,与 PCR 阳性的相关性更好。MLST 显示,感染 TPE 分离株的遗传多样性水平较低,仅代表三种不同的基因型(JE11、SE22 和 TE13)。两种以前使用的分型方案显示出相似的分辨率。证明了两个新等位基因(一个在 TP0858,一个在 TP0136)是由基因组内重组/缺失事件产生的。与被分型为 JE11 的样本相比,在有两个或更多溃疡的患者和有更高特异性 TP 血清学检测值的患者中,更频繁地检测到次要基因型(TE13 和 SE22)。此外,在三个 JE11 分离株的 23S rRNA 基因中发现了 A2058G 突变,导致阿奇霉素耐药。