Detection of pathogens associated with early-onset neonatal sepsis in cord blood at birth using quantitative PCR [version 2; peer review: 2 approved]

Background: Early onset neonatal sepsis (EONS) typically begins prior to, during or soon after birth and may be rapidly fatal. There is paucity of data on the aetiology of EONS in sub-Saharan Africa due to limited diagnostic capacity in this region, despite the associated significant mortality and l...

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Main Authors: Stella Mwakio, Anna C. Seale, Wilson Gumbi, Christina W. Obiero, Mami Taniuchi, James A. Berkley, Hope Mwangudzah, Eric Houpt, Jie Liu
Format: Article
Language:English
Published: Wellcome 2022-05-01
Series:Wellcome Open Research
Subjects:
Online Access:https://wellcomeopenresearch.org/articles/7-3/v2
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author Stella Mwakio
Anna C. Seale
Wilson Gumbi
Christina W. Obiero
Mami Taniuchi
James A. Berkley
Hope Mwangudzah
Eric Houpt
Jie Liu
author_facet Stella Mwakio
Anna C. Seale
Wilson Gumbi
Christina W. Obiero
Mami Taniuchi
James A. Berkley
Hope Mwangudzah
Eric Houpt
Jie Liu
author_sort Stella Mwakio
collection DOAJ
description Background: Early onset neonatal sepsis (EONS) typically begins prior to, during or soon after birth and may be rapidly fatal. There is paucity of data on the aetiology of EONS in sub-Saharan Africa due to limited diagnostic capacity in this region, despite the associated significant mortality and long-term neurological impairment. Methods: We compared pathogens detected in cord blood samples between neonates admitted to hospital with possible serious bacterial infection (pSBI) in the first 48 hours of life (cases) and neonates remaining well (controls). Cord blood was systematically collected at Kilifi County Hospital (KCH) from 2011-2016, and later tested for 21 bacterial, viral and protozoal targets using multiplex PCR via TaqMan Array Cards (TAC). Results: Among 603 cases (101 [17%] of whom died), 179 (30%) tested positive for ≥1 target and 37 (6.1%) tested positive for multiple targets. Klebsiella oxytoca, Escherichia coli/Shigella spp., Pseudomonas aeruginosa, and Streptococcus pyogenes were commonest. Among 300 controls, 79 (26%) tested positive for ≥1 target, 11 (3.7%) were positive for multiple targets, and K. oxytoca and P. aeruginosa were most common. Cumulative odds ratios across controls: cases (survived): cases (died) were E. coli/Shigella spp. 2.6 (95%CI 1.6-4.4); E. faecalis 4.0 (95%CI 1.1-15); S. agalactiae 4.5 (95%CI 1.6-13); Ureaplasma spp. 2.9 (95%CI 1.3-6.4); Enterovirus 9.1 (95%CI 2.3-37); and Plasmodium spp. 2.9 (95%CI 1.4-6.2). Excluding K. oxytoca and P. aeruginosa as likely contaminants, aetiology was attributed in 9.4% (95%CI 5.1-13) cases using TAC. Leading pathogen attributions by TAC were E. coli/Shigella spp. (3.5% (95%CI 1.7-5.3)) and Ureaplasma spp. (1.7% (95%CI 0.5-3.0)). Conclusions: Cord blood sample may be useful in describing EONS pathogens at birth, but more specific tests are needed for individual diagnosis. Careful sampling of cord blood using aseptic techniques is crucial to minimize contamination. In addition to culturable bacteria, Ureaplasma and Enterovirus were causes of EONS.
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spelling doaj.art-0f69c3dee3fc4c09936d518388a9c87f2022-12-22T03:28:14ZengWellcomeWellcome Open Research2398-502X2022-05-01719812Detection of pathogens associated with early-onset neonatal sepsis in cord blood at birth using quantitative PCR [version 2; peer review: 2 approved]Stella Mwakio0https://orcid.org/0000-0001-9803-0264Anna C. Seale1https://orcid.org/0000-0002-0129-3146Wilson Gumbi2Christina W. Obiero3https://orcid.org/0000-0002-9321-0183Mami Taniuchi4James A. Berkley5https://orcid.org/0000-0002-1236-849XHope Mwangudzah6https://orcid.org/0000-0003-1166-8965Eric Houpt7Jie Liu8Clinical research, KEMRI-Wellcome Trust Research Programme, Kilifi, KenyaClinical research, KEMRI-Wellcome Trust Research Programme, Kilifi, KenyaBioscience department, KEMRI-Wellcome Trust Research Programme, Kilifi, KenyaClinical research, KEMRI-Wellcome Trust Research Programme, Kilifi, KenyaDivision of Infectious Diseases and International Health, University of Virginia, Virginia, USAClinical research, KEMRI-Wellcome Trust Research Programme, Kilifi, KenyaClinical research, KEMRI-Wellcome Trust Research Programme, Kilifi, KenyaDivision of Infectious Diseases and International Health, University of Virginia, Virginia, USADivision of Infectious Diseases and International Health, University of Virginia, Virginia, USABackground: Early onset neonatal sepsis (EONS) typically begins prior to, during or soon after birth and may be rapidly fatal. There is paucity of data on the aetiology of EONS in sub-Saharan Africa due to limited diagnostic capacity in this region, despite the associated significant mortality and long-term neurological impairment. Methods: We compared pathogens detected in cord blood samples between neonates admitted to hospital with possible serious bacterial infection (pSBI) in the first 48 hours of life (cases) and neonates remaining well (controls). Cord blood was systematically collected at Kilifi County Hospital (KCH) from 2011-2016, and later tested for 21 bacterial, viral and protozoal targets using multiplex PCR via TaqMan Array Cards (TAC). Results: Among 603 cases (101 [17%] of whom died), 179 (30%) tested positive for ≥1 target and 37 (6.1%) tested positive for multiple targets. Klebsiella oxytoca, Escherichia coli/Shigella spp., Pseudomonas aeruginosa, and Streptococcus pyogenes were commonest. Among 300 controls, 79 (26%) tested positive for ≥1 target, 11 (3.7%) were positive for multiple targets, and K. oxytoca and P. aeruginosa were most common. Cumulative odds ratios across controls: cases (survived): cases (died) were E. coli/Shigella spp. 2.6 (95%CI 1.6-4.4); E. faecalis 4.0 (95%CI 1.1-15); S. agalactiae 4.5 (95%CI 1.6-13); Ureaplasma spp. 2.9 (95%CI 1.3-6.4); Enterovirus 9.1 (95%CI 2.3-37); and Plasmodium spp. 2.9 (95%CI 1.4-6.2). Excluding K. oxytoca and P. aeruginosa as likely contaminants, aetiology was attributed in 9.4% (95%CI 5.1-13) cases using TAC. Leading pathogen attributions by TAC were E. coli/Shigella spp. (3.5% (95%CI 1.7-5.3)) and Ureaplasma spp. (1.7% (95%CI 0.5-3.0)). Conclusions: Cord blood sample may be useful in describing EONS pathogens at birth, but more specific tests are needed for individual diagnosis. Careful sampling of cord blood using aseptic techniques is crucial to minimize contamination. In addition to culturable bacteria, Ureaplasma and Enterovirus were causes of EONS.https://wellcomeopenresearch.org/articles/7-3/v2Neonate sepsis molecular aetiology PCReng
spellingShingle Stella Mwakio
Anna C. Seale
Wilson Gumbi
Christina W. Obiero
Mami Taniuchi
James A. Berkley
Hope Mwangudzah
Eric Houpt
Jie Liu
Detection of pathogens associated with early-onset neonatal sepsis in cord blood at birth using quantitative PCR [version 2; peer review: 2 approved]
Wellcome Open Research
Neonate
sepsis
molecular
aetiology
PCR
eng
title Detection of pathogens associated with early-onset neonatal sepsis in cord blood at birth using quantitative PCR [version 2; peer review: 2 approved]
title_full Detection of pathogens associated with early-onset neonatal sepsis in cord blood at birth using quantitative PCR [version 2; peer review: 2 approved]
title_fullStr Detection of pathogens associated with early-onset neonatal sepsis in cord blood at birth using quantitative PCR [version 2; peer review: 2 approved]
title_full_unstemmed Detection of pathogens associated with early-onset neonatal sepsis in cord blood at birth using quantitative PCR [version 2; peer review: 2 approved]
title_short Detection of pathogens associated with early-onset neonatal sepsis in cord blood at birth using quantitative PCR [version 2; peer review: 2 approved]
title_sort detection of pathogens associated with early onset neonatal sepsis in cord blood at birth using quantitative pcr version 2 peer review 2 approved
topic Neonate
sepsis
molecular
aetiology
PCR
eng
url https://wellcomeopenresearch.org/articles/7-3/v2
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