Etiology of severe invasive infections in young infants in rural settings in sub-Saharan Africa.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2022
Historique:
received: 20 09 2021
accepted: 08 02 2022
entrez: 25 2 2022
pubmed: 26 2 2022
medline: 9 3 2022
Statut: epublish

Résumé

Serious invasive infections in newborns are a major cause of death. Lack of data on etiological causes hampers progress towards reduction of mortality. This study aimed to identify pathogens responsible for such infections in young infants in sub-Saharan Africa and to describe their antibiotics resistance profile. Between September 2016 and April 2018 we implemented an observational study in two rural sites in Burkina Faso and Tanzania enrolling young infants aged 0-59 days old with serious invasive infection. Blood samples underwent blood culture and molecular biology. In total 634 infants with clinical diagnosis of serious invasive infection were enrolled and 4.2% of the infants had a positive blood culture. The most frequent pathogens identified by blood culture were Klebsiella pneumonia and Staphylococcus aureus, followed by Escherichia coli. Gram-negative isolates were only partially susceptible to first line WHO recommended treatment for neonatal sepsis at community level. A total of 18.6% of the infants were PCR positive for at least one pathogen and Escherichia coli and Staphylococcus aureus were the most common bacteria detected. Among infants enrolled, 60/634 (9.5%) died. Positive blood culture but not positive PCR was associated with risk of death. For most deaths, no pathogen was identified either by blood culture or molecular testing, and hence a causal agent remained unclear. Mortality was associated with low body temperature, tachycardia, respiratory symptoms, convulsions, history of difficult feeding, movement only when stimulated or reduced level of consciousness, diarrhea and/or vomiting. While Klebsiella pneumonia and Staphylococcus aureus, as well as Escherichia coli were pathogens most frequently identified in infants with clinical suspicion of serious invasive infections, most cases remain without definite diagnosis, making more accurate diagnostic tools urgently needed. Antibiotics resistance to first line antibiotics is an increasing challenge even in rural Africa.

Sections du résumé

BACKGROUND
Serious invasive infections in newborns are a major cause of death. Lack of data on etiological causes hampers progress towards reduction of mortality. This study aimed to identify pathogens responsible for such infections in young infants in sub-Saharan Africa and to describe their antibiotics resistance profile.
METHODS
Between September 2016 and April 2018 we implemented an observational study in two rural sites in Burkina Faso and Tanzania enrolling young infants aged 0-59 days old with serious invasive infection. Blood samples underwent blood culture and molecular biology.
RESULTS
In total 634 infants with clinical diagnosis of serious invasive infection were enrolled and 4.2% of the infants had a positive blood culture. The most frequent pathogens identified by blood culture were Klebsiella pneumonia and Staphylococcus aureus, followed by Escherichia coli. Gram-negative isolates were only partially susceptible to first line WHO recommended treatment for neonatal sepsis at community level. A total of 18.6% of the infants were PCR positive for at least one pathogen and Escherichia coli and Staphylococcus aureus were the most common bacteria detected. Among infants enrolled, 60/634 (9.5%) died. Positive blood culture but not positive PCR was associated with risk of death. For most deaths, no pathogen was identified either by blood culture or molecular testing, and hence a causal agent remained unclear. Mortality was associated with low body temperature, tachycardia, respiratory symptoms, convulsions, history of difficult feeding, movement only when stimulated or reduced level of consciousness, diarrhea and/or vomiting.
CONCLUSION
While Klebsiella pneumonia and Staphylococcus aureus, as well as Escherichia coli were pathogens most frequently identified in infants with clinical suspicion of serious invasive infections, most cases remain without definite diagnosis, making more accurate diagnostic tools urgently needed. Antibiotics resistance to first line antibiotics is an increasing challenge even in rural Africa.

Identifiants

pubmed: 35213629
doi: 10.1371/journal.pone.0264322
pii: PONE-D-21-30404
pmc: PMC8880396
doi:

Types de publication

Clinical Trial Journal Article Multicenter Study Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0264322

Subventions

Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : World Health Organization
ID : 001
Pays : International
Organisme : NIAID NIH HHS
ID : K24 AI102972
Pays : United States

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Estomih Mduma (E)

Haydom Research Center, Haydom Lutheran Hospital, Haydom, United Republic of Tanzania.

Tinto Halidou (T)

Institut de Recherche en Sciences de la Santé (IRSS), Clinical Research Unit of Nanoro (CRUN), Nanoro, Burkina Faso.

Berenger Kaboré (B)

Institut de Recherche en Sciences de la Santé (IRSS), Clinical Research Unit of Nanoro (CRUN), Nanoro, Burkina Faso.

Thomas Walongo (T)

Haydom Research Center, Haydom Lutheran Hospital, Haydom, United Republic of Tanzania.

Palpouguini Lompo (P)

Institut de Recherche en Sciences de la Santé (IRSS), Clinical Research Unit of Nanoro (CRUN), Nanoro, Burkina Faso.

Justine Museveni (J)

Haydom Research Center, Haydom Lutheran Hospital, Haydom, United Republic of Tanzania.

Joshua Gidabayda (J)

Haydom Research Center, Haydom Lutheran Hospital, Haydom, United Republic of Tanzania.

Jean Gratz (J)

Division of Infectious Diseases and International Health, University of Virginia, Charlottesville, Virginia, United States of America.

Godfrey Guga (G)

Haydom Research Center, Haydom Lutheran Hospital, Haydom, United Republic of Tanzania.

Caroline Kimathi (C)

Haydom Research Center, Haydom Lutheran Hospital, Haydom, United Republic of Tanzania.

Jie Liu (J)

Division of Infectious Diseases and International Health, University of Virginia, Charlottesville, Virginia, United States of America.

Paschal Mdoe (P)

Haydom Research Center, Haydom Lutheran Hospital, Haydom, United Republic of Tanzania.

Robert Moshiro (R)

Haydom Research Center, Haydom Lutheran Hospital, Haydom, United Republic of Tanzania.

Max Petzold (M)

School of Public Health and Community Medicine, Institute of Medicine, University of Gothenburg, Gothenburg, Sweden.

Jan Singlovic (J)

UNICEF/UNDP/WB/WHO Special Program for Research & Training in Tropical Diseases (TDR), World Health Organization, Geneva, Switzerland.

Martine Guillerm (M)

UNICEF/UNDP/WB/WHO Special Program for Research & Training in Tropical Diseases (TDR), World Health Organization, Geneva, Switzerland.

Melba F Gomes (MF)

UNICEF/UNDP/WB/WHO Special Program for Research & Training in Tropical Diseases (TDR), World Health Organization, Geneva, Switzerland.

Eric R Houpt (ER)

Division of Infectious Diseases and International Health, University of Virginia, Charlottesville, Virginia, United States of America.

Christine M Halleux (CM)

UNICEF/UNDP/WB/WHO Special Program for Research & Training in Tropical Diseases (TDR), World Health Organization, Geneva, Switzerland.

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