Multicountry Distribution and Characterization of Extended-spectrum β-Lactamase-associated Gram-negative Bacteria from Bloodstream Infections in Sub-Saharan Africa

  • T. Toy
  • , G.D. Pak
  • , T.P. Duc
  • , J.I. Campbell
  • , M.A. El Tayeb
  • , V. Von Kalckreuth
  • , J. Im
  • , U. Panzner
  • , L.M. Cruz Espinoza
  • , D. Eibach
  • , D.M. Dekker
  • , S.E. Park
  • , H.J. Jeon
  • , F. Konings
  • , O.D. Mogeni
  • , L. Cosmas
  • , M. Bjerregaard-Andersen
  • , N. Gasmelseed
  • , J. T. Hertz
  • , A. Jaeger
  • R. Krumkamp, B. Ley, K. Thriemer, L.P. Kabore, A. Niang, T.M. Raminosoa, E. Sampo, N. Sarpong, A. Soura, E. Owusu-Dabo, M. Teferi, B. Yeshitela, S. Poppert, J. May, J.H. Kim, Y. Chon, J.K. Park, A. Aseffa, R.F. Breiman, H. Schütt-Gerowitt, P. Aaby, Y. Adu-Sarkodie, J.A. Crump, R. Rakotozandrindrainy, C. G. Meyer, A.G. Sow, J.D. Clemens, T.F. Wierzba, S. Baker, F. Marks

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Abstract

Background: Antimicrobial resistance (AMR) is a major global health concern, yet, there are noticeable gaps in AMR surveillance data in regions such as sub-Saharan Africa. We aimed to measure the prevalence of extended-spectrum β-lactamase (ESBL) producing Gram-negative bacteria in bloodstream infections from 12 sentinel sites in sub-Saharan Africa. Methods: Data were generated during the Typhoid Fever Surveillance in Africa Program (TSAP), in which standardized blood cultures were performed on febrile patients attending 12 health facilities in 9 sub-Saharan African countries between 2010 and 2014. Pathogenic bloodstream isolates were identified at the sites and then subsequently confirmed at a central reference laboratory. Antimicrobial susceptibility testing, detection of ESBL production, and conventional multiplex polymerase chain reaction (PCR) testing for genes encoding for β-lactamase were performed on all pathogens. Results: Five hundred and five pathogenic Gram-negative bloodstream isolates were isolated during the study period and available for further characterization. This included 423 Enterobacteriaceae. Phenotypically, 61 (12.1%) isolates exhibited ESBL activity, and genotypically, 47 (9.3%) yielded a PCR amplicon for at least one of the screened ESBL genes. Among specific Gram-negative isolates, 40 (45.5%) of 88 Klebsiella spp., 7 (5.7%) of 122 Escherichia coli, 6 (16.2%) of 37 Acinetobacter spp., and 2 (1.3%) of 159 of nontyphoidal Salmonella (NTS) showed phenotypic ESBL activity. Conclusions: Our findings confirm the presence of ESBL production among pathogens causing bloodstream infections in sub-Saharan Africa. With few alternatives for managing ESBL-producing pathogens in the African setting, measures to control the development and proliferation of AMR organisms are urgently needed.

OriginalsprogEngelsk
TidsskriftClinical Infectious Diseases
Vol/bind69
Udgave nummerSuppl. 6
Sider (fra-til)S449-S458
ISSN1058-4838
DOI
StatusUdgivet - 30. okt. 2019

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