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DOI 10.1093/cid/ciz450

Медицинская библиотека · Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2019

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

Toy Trevor, Pak Gi Deok, Duc Trung Pham, Campbell James I, El Tayeb Muna Ahmed, Von Kalckreuth Vera, Im Justin, Panzner Ursula, Cruz Espinoza Ligia Maria, Eibach Daniel, Dekker Denise Myriam, Park Se Eun, Jeon Hyon Jin, Konings Frank, Mogeni Ondari D, Cosmas Leonard, Bjerregaard-Andersen Morten, Gasmelseed Nagla, Hertz Julian T, Jaeger Anna, Krumkamp Ralf, Ley Benedikt, Thriemer Kamala, Kabore Leon Parfait, Niang Aissatou, Raminosoa Tiana Mirana, Sampo Emmanuel, Sarpong Nimako, Soura Abdramane, Owusu-Dabo Ellis, Teferi Mekonnen, Yeshitela Biruk, Poppert Sven, May Jürgen, Kim Jerome H, Chon Yun, Park Jin Kyung, Aseffa Abroaham, Breiman Robert F, Schütt-Gerowitt Heidi, Aaby Peter, Adu-Sarkodie Yaw, Crump John A, Rakotozandrindrainy Raphaël, Meyer Christian G, Sow Amy Gassama, Clemens John D, Wierzba Thomas F, Baker Stephen, Marks Florian

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Аннотация

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.

Для цитирования: Toy Trevor, Pak Gi Deok, Duc Trung Pham, Campbell James I, El Tayeb Muna Ahmed, Von Kalckreuth Vera, Im Justin, Panzner Ursula, Cruz Espinoza Ligia Maria, Eibach Daniel, Dekker Denise Myriam, Park Se Eun, Jeon Hyon Jin, Konings Frank, Mogeni Ondari D, Cosmas Leonard, Bjerregaard-Andersen Morten, Gasmelseed Nagla, Hertz Julian T, Jaeger Anna, Krumkamp Ralf, Ley Benedikt, Thriemer Kamala, Kabore Leon Parfait, Niang Aissatou, Raminosoa Tiana Mirana, Sampo Emmanuel, Sarpong Nimako, Soura Abdramane, Owusu-Dabo Ellis, Teferi Mekonnen, Yeshitela Biruk, Poppert Sven, May Jürgen, Kim Jerome H, Chon Yun, Park Jin Kyung, Aseffa Abroaham, Breiman Robert F, Schütt-Gerowitt Heidi, Aaby Peter, Adu-Sarkodie Yaw, Crump John A, Rakotozandrindrainy Raphaël, Meyer Christian G, Sow Amy Gassama, Clemens John D, Wierzba Thomas F, Baker Stephen, Marks Florian. Multicountry Distribution and Characterization of Extended-spectrum β-Lactamase-associated Gram-negative Bacteria From Bloodstream Infections in Sub-Saharan Africa.. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America. 2019. DOI: 10.1093/cid/ciz450.

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