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首页> 外文期刊>American journal of respiratory and critical care medicine >Widespread Colonization of the Lung by Tropheryma whipplei in HIV Infection
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Widespread Colonization of the Lung by Tropheryma whipplei in HIV Infection

机译:特发性疟原虫在艾滋病毒感染中对肺的广泛定植

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摘要

Rationale: Lung infections caused by opportunistic or virulent pathogens are a principal cause of morbidity and mortality in HIV infection. It is unknown whether HIV infection leads to changes in basal lung microflora, which may contribute to chronic pulmonary complications that increasingly are being recognized in individuals infected with HIV. Objectives: To determine whether the immunodeficiency associated with HIV infection resulted in alteration of the lung microbiota. Methods: We used 16S ribosomal RNA targeted pyrosequencing and shotgun metagenomic sequencing to analyze bacterial gene sequences in bronchoalveolar lavage (BAL) and mouths of 82 HIV-positive and 77 HIV-negative subjects. Measurements and Main Results: Sequences representing Tropheryma whipplei, the etiologic agent of Whipple's disease, were significantly more frequent in BAL of HIV-positive compared with HIV-negative individuals. T. whipplei dominated the community (>50% of sequence reads) in 11 HIV-positive subjects, but only 1 HIV-negative individual (13.4 versus 1.3%; P= 0.0018). In 30 HIV-positive individuals sampled longitudinally, antiretroviral therapy resulted in a significantly reduced relative abundance of T. whipplei in the lung. Shotgun metagenomic sequencing was performed on eight BAL samples dominated by T. whipplei 16S ribosomal RNA. Whole genome assembly of pooled reads showed that uncultured lung- derived T. whipplei had similar gene content to two isolates obtained from subjects with Whipple's disease. Conclusions: Asymptomatic subjects with HIV infection have unexpected colonization of the lung by T. whipplei, which is reduced by effective antiretroviral therapy and merits further study for a potential pathogenic role in chronic pulmonary complications of HIV infection.
机译:理由:机会性或致病性病原体引起的肺部感染是艾滋病毒感染发病率和死亡率的主要原因。尚不清楚HIV感染是否会导致基础肺部菌群的改变,这可能会导致慢性肺部并发症,而在感染了HIV的个体中这种病越来越多地被认识到。目的:确定与艾滋病毒感染相关的免疫缺陷是否导致肺微生物群的改变。方法:我们使用针对16S核糖体RNA的焦磷酸测序和shot弹枪宏基因组测序,分析了82名HIV阳性和77名HIV阴性受试者的支气管肺泡灌洗(BAL)和口腔中的细菌基因序列。测量结果和主要结果:与HIV阴性个体相比,代表Whipple's病病原体的惠特勒麻风菌的序列在HIV阳性BAL中的发生率明显更高。 T. whipplei在11个HIV阳性受试者中占主导地位(超过50%的序列读数),但只有1个HIV阴性个体(13.4对1.3%; P = 0.0018)。在纵向取样的30个HIV阳性个体中,抗逆转录病毒疗法导致肺部T. whipplei的相对丰度大大降低。 gun弹枪宏基因组测序是在八株以T.whipplei 16S核糖体RNA为主的BAL样品上进行的。汇集的读物的全基因组组装显示,未培养的肺源鞭毛木犀具有与从Whipple病受试者获得的两个分离株相似的基因含量。结论:无症状的HIV感染者可通过T. whipplei意外地在肺部定植,有效的抗逆转录病毒疗法可减少其定植,值得进一步研究其在HIV慢性肺部并发症中的潜在致病作用。

著录项

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  • 作者单位

    Department of Chemistry and Biochemistry and Biofrontiers Institute, University of Colorado, Boulder, Colorado;

    Department of Medicine, University of Colorado Denver, Aurora, Colorado;

    Department of Medicine, University of Colorado Denver, Aurora, Colorado;

    Department of Medicine, University of Colorado Denver, Aurora, Colorado;

    Departments of Medicine and Microbiology, University of Pennsylvania, Philadelphia, Pennsylvania;

    The Genome Institute, Washington University, St. Louis, Missouri;

    The Genome Institute, Washington University, St. Louis, Missouri;

    The Genome Institute, Washington University, St. Louis, Missouri;

    The Genome Institute, Washington University, St. Louis, Missouri;

    The Genome Institute, Washington University, St. Louis, Missouri;

    Department of Medicine, University of Colorado Denver, Aurora, Colorado;

    Department of Medicine, University of Colorado Denver, Aurora, Colorado;

    Department of Chemistry and Biochemistry and Biofrontiers Institute, University of Colorado, Boulder, Colorado;

    Department of Chemistry and Biochemistry and Biofrontiers Institute, University of Colorado, Boulder, Colorado;

    Department of Chemistry and Biochemistry and Biofrontiers Institute, University of Colorado, Boulder, Colorado;

    Department of Medicine, University of Colorado Denver, Aurora, Colorado,epartment of Internal Medicine, University of Michigan, Ann Arbor, Michigan;

    epartment of Internal Medicine, University of Michigan, Ann Arbor, Michigan;

    epartment of Internal Medicine, University of Michigan, Ann Arbor, Michigan;

    Department of Medicine, University of California San Francisco, San Francisco, California;

    Department of Medicine, University of California San Francisco, San Francisco, California;

    The Genome Institute, Washington University, St. Louis, Missouri;

    Department of Medicine, University of Arizona, Tucson, Arizona;

    Department of Medicine, Indiana University, Indianapolis, Indiana;

    Departments of Medicine and Computational and Systems Biology, University of Pittsburgh, Pittsburgh, Pennsylvania;

    Departments of Medicine and Computational and Systems Biology, University of Pittsburgh, Pittsburgh, Pennsylvania;

    Departments of Medicine and Microbiology, University of Pennsylvania, Philadelphia, Pennsylvania;

    Departments of Medicine and Microbiology, University of Pennsylvania, Philadelphia, Pennsylvania;

    Department of Chemistry and Biochemistry and Biofrontiers Institute, University of Colorado, Boulder, Colorado,Howard Hughes Medical Institute, Boulder, Colorado;

    Department of Medicine, University of Colorado Denver, Aurora, Colorado;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    human; microbiome; metagenome; 16S ribosomal RNA; bronchoalveolar lavage;

    机译:人微生物组元基因组16S核糖体RNA;支气管肺泡灌洗;

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