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化脓性链球菌与雅司病流行岛屿上儿童特发性皮肤溃疡有关。

Streptococcus pyogenes Is Associated with Idiopathic Cutaneous Ulcers in Children on a Yaws-Endemic Island.

机构信息

Department of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, Indiana, USA

Carretera de Canyet, Hospital Universitari Germans Trias i Pujol, Badalona, Barcelona, Spain.

出版信息

mBio. 2021 Jan 12;12(1):e03162-20. doi: 10.1128/mBio.03162-20.

DOI:10.1128/mBio.03162-20
PMID:33436440
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7844543/
Abstract

Exudative cutaneous ulcers (CU) in yaws-endemic areas are associated with subsp. (TP) and (HD), but one-third of CU cases are idiopathic (IU). Using mass drug administration (MDA) of azithromycin, a yaws eradication campaign on Lihir Island in Papua New Guinea reduced but failed to eradicate yaws; IU rates remained constant throughout the campaign. To identify potential etiologies of IU, we obtained swabs of CU lesions ( = 279) and of the skin of asymptomatic controls (AC;  = 233) from the Lihir Island cohort and characterized their microbiomes using a metagenomics approach. CU bacterial communities were less diverse than those of the AC. Using real-time multiplex PCR with pathogen-specific primers, we separated CU specimens into HD-positive (HD+), TP+, HD+TP+, and IU groups. Each CU subgroup formed a distinct bacterial community, defined by the species detected and/or the relative abundances of species within each group. was the most abundant organism in IU (22.65%) and was enriched in IU compared to other ulcer groups. Follow-up samples ( = 31) were obtained from nonhealed ulcers; the average relative abundance of was 30.11% in not improved ulcers and 0.88% in improved ulcers, suggesting that in the not improved ulcers may be azithromycin resistant. was enriched in IU that lacked As some and TP strains are macrolide resistant, penicillin may be the drug of choice for CU azithromycin treatment failures. Our study will aid in the design of diagnostic tests and selective therapies for CU. Cutaneous ulcers (CU) affect approximately 100,000 children in the tropics each year. While two-thirds of CU are caused by subspecies and , the cause(s) of the remaining one-third is unknown. Given the failure of mass drug administration of azithromycin to eradicate CU, the World Health Organization recently proposed an integrated disease management strategy to control CU. Success of this strategy requires determining the unknown cause(s) of CU. By using 16S rRNA gene sequencing of swabs obtained from CU and the skin of asymptomatic children, we identified another possible cause of skin ulcers, Although is known to cause impetigo and cellulitis, this is the first report implicating the organism as a causal agent of CU. Inclusion of into the integrated disease management plan will improve diagnostic testing and treatment of this painful and debilitating disease of children and strengthen elimination efforts.

摘要

渗出性皮肤溃疡(CU)在雅司病流行地区与 亚种(TP)和 亚种(HD)有关,但三分之一的 CU 病例是特发性的(IU)。在巴布亚新几内亚利希尔岛开展的大规模药物治疗(MDA)用阿奇霉素治疗雅司病,虽然降低了但未能根除雅司病;整个运动期间 IU 发病率保持不变。为了确定 IU 的潜在病因,我们从利希尔岛队列中获得了 CU 病变的拭子( = 279)和无症状对照者(AC)的皮肤拭子( = 233),并使用宏基因组学方法对其微生物组进行了表征。CU 的细菌群落多样性低于 AC。使用带有病原体特异性引物的实时多重 PCR,我们将 CU 标本分为 HD 阳性(HD+)、TP+、HD+TP+和 IU 组。每个 CU 亚组形成一个独特的细菌群落,由每个组中检测到的物种和/或物种的相对丰度定义。 在 IU(22.65%)中最为丰富,与其他溃疡组相比,在 IU 中更为丰富。从未愈合的溃疡中获得了随访样本( = 31);未改善的溃疡中 的平均相对丰度为 30.11%,改善的溃疡中的相对丰度为 0.88%,表明未改善的溃疡中的 可能对阿奇霉素有耐药性。 在缺乏 的 IU 中富集。由于一些 和 TP 菌株对大环内酯类药物有耐药性,因此青霉素可能是治疗 CU 阿奇霉素治疗失败的首选药物。我们的研究将有助于为 CU 设计诊断测试和选择性治疗方法。每年热带地区约有 10 万名儿童患有皮肤溃疡(CU)。虽然三分之二的 CU 是由亚种 和 引起的,但其余三分之一的病因尚不清楚。鉴于大规模使用阿奇霉素进行药物治疗未能根除 CU,世界卫生组织最近提出了一项综合疾病管理策略来控制 CU。该策略的成功需要确定 CU 的未知病因。通过对从 CU 和无症状儿童皮肤中获得的拭子进行 16S rRNA 基因测序,我们确定了另一种可能导致皮肤溃疡的原因, 尽管 已知会引起脓疱疮和蜂窝织炎,但这是首次将该病原体与 CU 联系起来的报告。将 纳入综合疾病管理计划将改善对这种痛苦和使人虚弱的儿童疾病的诊断测试和治疗,并加强消除工作。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8119/7844543/41255fa1be14/mBio.03162-20-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8119/7844543/a6814ca264d7/mBio.03162-20-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8119/7844543/847f7d48d41b/mBio.03162-20-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8119/7844543/544b9e080673/mBio.03162-20-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8119/7844543/41255fa1be14/mBio.03162-20-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8119/7844543/a6814ca264d7/mBio.03162-20-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8119/7844543/847f7d48d41b/mBio.03162-20-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8119/7844543/544b9e080673/mBio.03162-20-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8119/7844543/41255fa1be14/mBio.03162-20-f0004.jpg

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