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Separating Putative Pathogens from Background Contamination with Principal Orthogonal Decomposition: Evidence for Leptospira in the Ugandan Neonatal Septisome

Neonatal sepsis (NS) is responsible for over 1 million yearly deaths worldwide. In the developing world, NS is often treated without an identified microbial pathogen. Amplicon sequencing of the bacterial 16S rRNA gene can be used to identify organisms that are difficult to detect by routine microbio...

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Autores principales: Schiff, Steven J., Kiwanuka, Julius, Riggio, Gina, Nguyen, Lan, Mu, Kevin, Sproul, Emily, Bazira, Joel, Mwanga-Amumpaire, Juliet, Tumusiime, Dickson, Nyesigire, Eunice, Lwanga, Nkangi, Bogale, Kaleb T., Kapur, Vivek, Broach, James R., Morton, Sarah U., Warf, Benjamin C., Poss, Mary
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4904006/
https://www.ncbi.nlm.nih.gov/pubmed/27379237
http://dx.doi.org/10.3389/fmed.2016.00022
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author Schiff, Steven J.
Kiwanuka, Julius
Riggio, Gina
Nguyen, Lan
Mu, Kevin
Sproul, Emily
Bazira, Joel
Mwanga-Amumpaire, Juliet
Tumusiime, Dickson
Nyesigire, Eunice
Lwanga, Nkangi
Bogale, Kaleb T.
Kapur, Vivek
Broach, James R.
Morton, Sarah U.
Warf, Benjamin C.
Poss, Mary
author_facet Schiff, Steven J.
Kiwanuka, Julius
Riggio, Gina
Nguyen, Lan
Mu, Kevin
Sproul, Emily
Bazira, Joel
Mwanga-Amumpaire, Juliet
Tumusiime, Dickson
Nyesigire, Eunice
Lwanga, Nkangi
Bogale, Kaleb T.
Kapur, Vivek
Broach, James R.
Morton, Sarah U.
Warf, Benjamin C.
Poss, Mary
author_sort Schiff, Steven J.
collection PubMed
description Neonatal sepsis (NS) is responsible for over 1 million yearly deaths worldwide. In the developing world, NS is often treated without an identified microbial pathogen. Amplicon sequencing of the bacterial 16S rRNA gene can be used to identify organisms that are difficult to detect by routine microbiological methods. However, contaminating bacteria are ubiquitous in both hospital settings and research reagents and must be accounted for to make effective use of these data. In this study, we sequenced the bacterial 16S rRNA gene obtained from blood and cerebrospinal fluid (CSF) of 80 neonates presenting with NS to the Mbarara Regional Hospital in Uganda. Assuming that patterns of background contamination would be independent of pathogenic microorganism DNA, we applied a novel quantitative approach using principal orthogonal decomposition to separate background contamination from potential pathogens in sequencing data. We designed our quantitative approach contrasting blood, CSF, and control specimens and employed a variety of statistical random matrix bootstrap hypotheses to estimate statistical significance. These analyses demonstrate that Leptospira appears present in some infants presenting within 48 h of birth, indicative of infection in utero, and up to 28 days of age, suggesting environmental exposure. This organism cannot be cultured in routine bacteriological settings and is enzootic in the cattle that often live in close proximity to the rural peoples of western Uganda. Our findings demonstrate that statistical approaches to remove background organisms common in 16S sequence data can reveal putative pathogens in small volume biological samples from newborns. This computational analysis thus reveals an important medical finding that has the potential to alter therapy and prevention efforts in a critically ill population.
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spelling pubmed-49040062016-07-04 Separating Putative Pathogens from Background Contamination with Principal Orthogonal Decomposition: Evidence for Leptospira in the Ugandan Neonatal Septisome Schiff, Steven J. Kiwanuka, Julius Riggio, Gina Nguyen, Lan Mu, Kevin Sproul, Emily Bazira, Joel Mwanga-Amumpaire, Juliet Tumusiime, Dickson Nyesigire, Eunice Lwanga, Nkangi Bogale, Kaleb T. Kapur, Vivek Broach, James R. Morton, Sarah U. Warf, Benjamin C. Poss, Mary Front Med (Lausanne) Medicine Neonatal sepsis (NS) is responsible for over 1 million yearly deaths worldwide. In the developing world, NS is often treated without an identified microbial pathogen. Amplicon sequencing of the bacterial 16S rRNA gene can be used to identify organisms that are difficult to detect by routine microbiological methods. However, contaminating bacteria are ubiquitous in both hospital settings and research reagents and must be accounted for to make effective use of these data. In this study, we sequenced the bacterial 16S rRNA gene obtained from blood and cerebrospinal fluid (CSF) of 80 neonates presenting with NS to the Mbarara Regional Hospital in Uganda. Assuming that patterns of background contamination would be independent of pathogenic microorganism DNA, we applied a novel quantitative approach using principal orthogonal decomposition to separate background contamination from potential pathogens in sequencing data. We designed our quantitative approach contrasting blood, CSF, and control specimens and employed a variety of statistical random matrix bootstrap hypotheses to estimate statistical significance. These analyses demonstrate that Leptospira appears present in some infants presenting within 48 h of birth, indicative of infection in utero, and up to 28 days of age, suggesting environmental exposure. This organism cannot be cultured in routine bacteriological settings and is enzootic in the cattle that often live in close proximity to the rural peoples of western Uganda. Our findings demonstrate that statistical approaches to remove background organisms common in 16S sequence data can reveal putative pathogens in small volume biological samples from newborns. This computational analysis thus reveals an important medical finding that has the potential to alter therapy and prevention efforts in a critically ill population. Frontiers Media S.A. 2016-06-13 /pmc/articles/PMC4904006/ /pubmed/27379237 http://dx.doi.org/10.3389/fmed.2016.00022 Text en Copyright © 2016 Schiff, Kiwanuka, Riggio, Nguyen, Mu, Sproul, Bazira, Mwanga-Amumpaire, Tumusiime, Nyesigire, Lwanga, Bogale, Kapur, Broach, Morton, Warf and Poss. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Schiff, Steven J.
Kiwanuka, Julius
Riggio, Gina
Nguyen, Lan
Mu, Kevin
Sproul, Emily
Bazira, Joel
Mwanga-Amumpaire, Juliet
Tumusiime, Dickson
Nyesigire, Eunice
Lwanga, Nkangi
Bogale, Kaleb T.
Kapur, Vivek
Broach, James R.
Morton, Sarah U.
Warf, Benjamin C.
Poss, Mary
Separating Putative Pathogens from Background Contamination with Principal Orthogonal Decomposition: Evidence for Leptospira in the Ugandan Neonatal Septisome
title Separating Putative Pathogens from Background Contamination with Principal Orthogonal Decomposition: Evidence for Leptospira in the Ugandan Neonatal Septisome
title_full Separating Putative Pathogens from Background Contamination with Principal Orthogonal Decomposition: Evidence for Leptospira in the Ugandan Neonatal Septisome
title_fullStr Separating Putative Pathogens from Background Contamination with Principal Orthogonal Decomposition: Evidence for Leptospira in the Ugandan Neonatal Septisome
title_full_unstemmed Separating Putative Pathogens from Background Contamination with Principal Orthogonal Decomposition: Evidence for Leptospira in the Ugandan Neonatal Septisome
title_short Separating Putative Pathogens from Background Contamination with Principal Orthogonal Decomposition: Evidence for Leptospira in the Ugandan Neonatal Septisome
title_sort separating putative pathogens from background contamination with principal orthogonal decomposition: evidence for leptospira in the ugandan neonatal septisome
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4904006/
https://www.ncbi.nlm.nih.gov/pubmed/27379237
http://dx.doi.org/10.3389/fmed.2016.00022
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