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      Cotrimoxazole Prophylaxis Increases Resistance Gene Prevalence and α-Diversity but Decreases β-Diversity in the Gut Microbiome of Human Immunodeficiency Virus–Exposed, Uninfected Infants

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          Abstract

          Background

          Prophylactic cotrimoxazole treatment is recommended in human immunodeficiency virus (HIV)–exposed, uninfected (HEU) infants, but the effects of this treatment on developing HEU infant gut microbiotas and resistomes are largely undefined.

          Methods

          We analyzed whole-metagenome sequencing data from 163 longitudinally collected stool samples from 63 HEU infants randomized to receive (n = 34; CTX-T) or to not receive (n = 29; CTX-N) prophylactic cotrimoxazole treatment. We generated taxonomic, functional pathway, and resistance gene profiles for each sample and compared microbiome signatures between the CTX-T and CTX-N infants.

          Results

          Metagenomic analysis did not reveal significant differences in taxonomic or functional pathway α-diversity between CTX-T and CTX-N infants. In contrast, resistance gene prevalence ( P = .00719) and α-diversity ( P = .0045) increased in CTX-T infants. These differences increased over time for both resistance gene prevalence measured by log-normalized abundance (4-month mean, 0.71 [95% confidence interval {CI}, .2–1.2] and 6-month mean, 0.85 [95% CI, .1–1.7]) and α-diversity ( P = .0045). Unlike α-diversity, interindividual gut microbiome taxonomic (mean, −0.11 [95% CI, −.15 to −.077]), functional taxonomic (mean, −0.050 [95% CI, −.084 to −.017]), and resistance gene (mean, −0.13 [95% CI, −.17 to −.099]) β-diversity decreased in CTX-T infants compared with CTX-N infants. These results are consistent with persistent antibiotic selection pressure.

          Conclusions

          Cotrimoxazole prophylaxis in HEU infants decreased gut microbiome β-diversity and increased antibiotic resistance gene α-diversity and prevalence. Antibiotic resistance is a growing threat, especially in low- and middle-income countries where the higher perinatal HIV exposure rates result in cotrimoxazole prophylaxis. Understanding effects from current HEU infant antibiotic prophylaxis guidelines will inform guideline revisions and efforts to reduce increasing antibiotic resistance.

          Abstract

          Cotrimoxazole treatment in HIV-exposed, uninfected (HEU) infants increases resistance gene prevalence and α-diversity, and decreases microbial taxonomic, functional pathway, and resistance gene β-diversity. Future HEU infant prophylaxis recommendations should consider these findings given rising global antibiotic resistance.

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          Most cited references71

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          Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing

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            Trimmomatic: a flexible trimmer for Illumina sequence data

            Motivation: Although many next-generation sequencing (NGS) read preprocessing tools already existed, we could not find any tool or combination of tools that met our requirements in terms of flexibility, correct handling of paired-end data and high performance. We have developed Trimmomatic as a more flexible and efficient preprocessing tool, which could correctly handle paired-end data. Results: The value of NGS read preprocessing is demonstrated for both reference-based and reference-free tasks. Trimmomatic is shown to produce output that is at least competitive with, and in many cases superior to, that produced by other tools, in all scenarios tested. Availability and implementation: Trimmomatic is licensed under GPL V3. It is cross-platform (Java 1.5+ required) and available at http://www.usadellab.org/cms/index.php?page=trimmomatic Contact: usadel@bio1.rwth-aachen.de Supplementary information: Supplementary data are available at Bioinformatics online.
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              Structure, Function and Diversity of the Healthy Human Microbiome

              Studies of the human microbiome have revealed that even healthy individuals differ remarkably in the microbes that occupy habitats such as the gut, skin, and vagina. Much of this diversity remains unexplained, although diet, environment, host genetics, and early microbial exposure have all been implicated. Accordingly, to characterize the ecology of human-associated microbial communities, the Human Microbiome Project has analyzed the largest cohort and set of distinct, clinically relevant body habitats to date. We found the diversity and abundance of each habitat’s signature microbes to vary widely even among healthy subjects, with strong niche specialization both within and among individuals. The project encountered an estimated 81–99% of the genera, enzyme families, and community configurations occupied by the healthy Western microbiome. Metagenomic carriage of metabolic pathways was stable among individuals despite variation in community structure, and ethnic/racial background proved to be one of the strongest associations of both pathways and microbes with clinical metadata. These results thus delineate the range of structural and functional configurations normal in the microbial communities of a healthy population, enabling future characterization of the epidemiology, ecology, and translational applications of the human microbiome.
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                Author and article information

                Journal
                Clin Infect Dis
                Clin Infect Dis
                cid
                Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America
                Oxford University Press (US )
                1058-4838
                1537-6591
                01 December 2020
                13 December 2019
                13 December 2019
                : 71
                : 11
                : 2858-2868
                Affiliations
                [1 ] Edison Family Center for Genome Sciences and Systems Biology, Washington University in St Louis School of Medicine, St Louis, Missouri, USA
                [2 ] Department of Paediatrics and Child Health, University of KwaZulu-Natal, Durban, South Africa
                [3 ] Department of Pathology and Immunology, Washington University in St Louis School of Medicine, St Louis, Missouri, USA
                [4 ] HIV Preventin Research Unit, South African Medical Research Council , Durban, South Africa
                [5 ] Department of Pediatrics, Washington University in St Louis School of Medicine, St Louis, Missouri, USA
                [6 ] Department of Molecular Microbiology, Washington University in St Louis School of Medicine, St Louis, Missouri, USA
                [7 ] Department of Biomedical Engineering, Washington University in St Louis, St Louis, Missouri, USA
                Author notes
                Correspondence: G. Dantas, Couch Biomedical Research, Building 4515 McKinley Ave, Rm 5314, Box 8510, St Louis, MO 63110 ( dantas@ 123456wustl.edu ).

                A. W. D. and E. M.-G. contributed equally to this work.

                Author information
                http://orcid.org/0000-0002-8744-8136
                http://orcid.org/0000-0003-0455-8370
                Article
                ciz1186
                10.1093/cid/ciz1186
                7778358
                31832638
                60d3e5fb-71a8-4465-aaa2-418e6824e496
                © The Author(s) 2019. Published by Oxford University Press for the Infectious Diseases Society of America.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 28 June 2019
                : 11 December 2019
                : 05 December 2019
                : 24 February 2020
                Page count
                Pages: 13
                Funding
                Funded by: National Institute of General Medical Sciences, DOI 10.13039/100000057;
                Award ID: R01 GM099538
                Funded by: National Institute of Allergy and Infectious Diseases, DOI 10.13039/100000060;
                Award ID: R01 AI123394
                Funded by: Eunice Kennedy Shriver National Institute of Child Health and Human Development, DOI 10.13039/100009633;
                Award ID: R01 HD092414
                Funded by: Bill & Melinda Gates Foundation, DOI 10.13039/100000865;
                Award ID: OPP1161117
                Funded by: National Institutes of Health, DOI 10.13039/100000002;
                Categories
                Major Articles and Commentaries
                AcademicSubjects/MED00290

                Infectious disease & Microbiology
                cotrimoxazole prophylaxis,antibiotic resistance,hiv-exposed,uninfected infant,microbiome

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