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The Problem of Microbial Dark Matter in Neonatal Sepsis

Neonatal sepsis (NS) kills 750,000 infants every year. Effectively treating NS requires timely diagnosis and antimicrobial therapy matched to the causative pathogens, but most blood cultures for suspected NS do not recover a causative pathogen. We refer to these suspected but unidentified pathogens...

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Detalles Bibliográficos
Autores principales: Sinnar, Shamim A., Schiff, Steven J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Centers for Disease Control and Prevention 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7588532/
https://www.ncbi.nlm.nih.gov/pubmed/33080169
http://dx.doi.org/10.3201/eid2611.200004
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author Sinnar, Shamim A.
Schiff, Steven J.
author_facet Sinnar, Shamim A.
Schiff, Steven J.
author_sort Sinnar, Shamim A.
collection PubMed
description Neonatal sepsis (NS) kills 750,000 infants every year. Effectively treating NS requires timely diagnosis and antimicrobial therapy matched to the causative pathogens, but most blood cultures for suspected NS do not recover a causative pathogen. We refer to these suspected but unidentified pathogens as microbial dark matter. Given these low culture recovery rates, many non–culture-based technologies are being explored to diagnose NS, including PCR, 16S amplicon sequencing, and whole metagenomic sequencing. However, few of these newer technologies are scalable or sustainable globally. To reduce worldwide deaths from NS, one possibility may be performing population-wide pathogen discovery. Because pathogen transmission patterns can vary across space and time, computational models can be built to predict the pathogens responsible for NS by region and season. This approach could help to optimally treat patients, decreasing deaths from NS and increasing antimicrobial stewardship until effective diagnostics that are scalable become available globally.
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spelling pubmed-75885322020-11-01 The Problem of Microbial Dark Matter in Neonatal Sepsis Sinnar, Shamim A. Schiff, Steven J. Emerg Infect Dis Perspective Neonatal sepsis (NS) kills 750,000 infants every year. Effectively treating NS requires timely diagnosis and antimicrobial therapy matched to the causative pathogens, but most blood cultures for suspected NS do not recover a causative pathogen. We refer to these suspected but unidentified pathogens as microbial dark matter. Given these low culture recovery rates, many non–culture-based technologies are being explored to diagnose NS, including PCR, 16S amplicon sequencing, and whole metagenomic sequencing. However, few of these newer technologies are scalable or sustainable globally. To reduce worldwide deaths from NS, one possibility may be performing population-wide pathogen discovery. Because pathogen transmission patterns can vary across space and time, computational models can be built to predict the pathogens responsible for NS by region and season. This approach could help to optimally treat patients, decreasing deaths from NS and increasing antimicrobial stewardship until effective diagnostics that are scalable become available globally. Centers for Disease Control and Prevention 2020-11 /pmc/articles/PMC7588532/ /pubmed/33080169 http://dx.doi.org/10.3201/eid2611.200004 Text en https://creativecommons.org/licenses/by/4.0/This is a publication of the U.S. Government. This publication is in the public domain and is therefore without copyright. All text from this work may be reprinted freely. Use of these materials should be properly cited.
spellingShingle Perspective
Sinnar, Shamim A.
Schiff, Steven J.
The Problem of Microbial Dark Matter in Neonatal Sepsis
title The Problem of Microbial Dark Matter in Neonatal Sepsis
title_full The Problem of Microbial Dark Matter in Neonatal Sepsis
title_fullStr The Problem of Microbial Dark Matter in Neonatal Sepsis
title_full_unstemmed The Problem of Microbial Dark Matter in Neonatal Sepsis
title_short The Problem of Microbial Dark Matter in Neonatal Sepsis
title_sort problem of microbial dark matter in neonatal sepsis
topic Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7588532/
https://www.ncbi.nlm.nih.gov/pubmed/33080169
http://dx.doi.org/10.3201/eid2611.200004
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