Molecular characterization of invasive Enterobacteriaceae from pediatric patients in Central and Northwestern Nigeria.


Journal

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

Informations de publication

Date de publication:
2020
Historique:
received: 18 02 2020
accepted: 01 09 2020
entrez: 26 10 2020
pubmed: 27 10 2020
medline: 13 11 2020
Statut: epublish

Résumé

Bacteremia is a leading cause of mortality in developing countries, however, etiologic evaluation is infrequent and empiric antibiotic use not evidence-based. Here, we evaluated the patterns of ESBL resistance in children enrolled into a surveillance study for community acquired bacteremic syndromes across health facilities in Central and Northwestern Nigeria. Blood culture was performed for children aged less than 5 years suspected of having sepsis from Sept 2008-Dec 2016. Blood was incubated using the BACTEC00AE system and Enterobacteriacea identified to the species level using Analytical Profile Index (API20E®). Antibiotic susceptibility profile was determined by the disc diffusion method. Real time PCR was used to characterize genes responsible for ESBL production. Of 21,000 children screened from Sept 2008-Dec 2016, 2,625(12.5%) were culture-positive. A total of 413 Enterobacteriaceae available for analysis were screened for ESBL. ESBL production was detected in 160 Enterobacteriaceae, high resistance rates were observed among ESBL-positive isolates for Ceftriaxone (92.3%), Aztreonam (96.8%), Cefpodoxime (96.3%), Cefotaxime (98.8%) and Trimethoprim/sulfamethoxazole (90%), while 87.5%, 90.7%, and 91.9% of the isolates were susceptible to Imipenem, Amikacin and Meropenem respectively. Frequently detected resistance genes were blaTEM-83.8% (134/160), and, blaCTX-M 83.1% (133/160) followed by blaSHVgenes 66.3% (106/160). Co-existence of blaCTX-M, blaTEM and blaSHV was seen in 94/160 (58.8%), blaCTX-M and blaTEM in 118/160 (73.8%), blaTEM and blaSHV in 97/160 (60.6%) and blaCTX-M and blaSHV in 100/160 (62.5%) of isolates tested. Our results indicate a high prevalence of bacteremia from ESBL Enterobacteriaceae in this population of children. These are resistant to commonly used antibiotics and careful choice of antibiotic treatment options is critical. Further studies to evaluate transmission dynamics of resistance genes could help in the reduction of ESBL resistance in these settings.

Sections du résumé

BACKGROUND
Bacteremia is a leading cause of mortality in developing countries, however, etiologic evaluation is infrequent and empiric antibiotic use not evidence-based. Here, we evaluated the patterns of ESBL resistance in children enrolled into a surveillance study for community acquired bacteremic syndromes across health facilities in Central and Northwestern Nigeria.
METHOD
Blood culture was performed for children aged less than 5 years suspected of having sepsis from Sept 2008-Dec 2016. Blood was incubated using the BACTEC00AE system and Enterobacteriacea identified to the species level using Analytical Profile Index (API20E®). Antibiotic susceptibility profile was determined by the disc diffusion method. Real time PCR was used to characterize genes responsible for ESBL production.
RESULT
Of 21,000 children screened from Sept 2008-Dec 2016, 2,625(12.5%) were culture-positive. A total of 413 Enterobacteriaceae available for analysis were screened for ESBL. ESBL production was detected in 160 Enterobacteriaceae, high resistance rates were observed among ESBL-positive isolates for Ceftriaxone (92.3%), Aztreonam (96.8%), Cefpodoxime (96.3%), Cefotaxime (98.8%) and Trimethoprim/sulfamethoxazole (90%), while 87.5%, 90.7%, and 91.9% of the isolates were susceptible to Imipenem, Amikacin and Meropenem respectively. Frequently detected resistance genes were blaTEM-83.8% (134/160), and, blaCTX-M 83.1% (133/160) followed by blaSHVgenes 66.3% (106/160). Co-existence of blaCTX-M, blaTEM and blaSHV was seen in 94/160 (58.8%), blaCTX-M and blaTEM in 118/160 (73.8%), blaTEM and blaSHV in 97/160 (60.6%) and blaCTX-M and blaSHV in 100/160 (62.5%) of isolates tested.
CONCLUSION
Our results indicate a high prevalence of bacteremia from ESBL Enterobacteriaceae in this population of children. These are resistant to commonly used antibiotics and careful choice of antibiotic treatment options is critical. Further studies to evaluate transmission dynamics of resistance genes could help in the reduction of ESBL resistance in these settings.

Identifiants

pubmed: 33104733
doi: 10.1371/journal.pone.0230037
pii: PONE-D-20-04796
pmc: PMC7588054
doi:

Substances chimiques

Anti-Bacterial Agents 0

Types de publication

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

e0230037

Subventions

Organisme : NIAID NIH HHS
ID : R01 AI097493
Pays : United States

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Carissa Duru (C)

International Foundation Against Infectious Diseases in Nigeria, Abuja, Nigeria.

Grace Olanipekun (G)

International Foundation Against Infectious Diseases in Nigeria, Abuja, Nigeria.

Vivian Odili (V)

International Foundation Against Infectious Diseases in Nigeria, Abuja, Nigeria.

Nicholas Kocmich (N)

Department of Pediatric Infectious Diseases, University of Nebraska Medical Center, Omaha, Nebraska, United States of America.

Amy Rezac (A)

Department of Pediatric Infectious Diseases, University of Nebraska Medical Center, Omaha, Nebraska, United States of America.

Theresa O Ajose (TO)

International Foundation Against Infectious Diseases in Nigeria, Abuja, Nigeria.

Nubwa Medugu (N)

Department of Medical Microbiology and Parasitology, National Hospital Abuja, International Foundation Against Infectious Diseases in Nigeria, Abuja, Nigeria.

Dominic Umoru (D)

Maitama District Hospital, Abuja, Nigeria.

Chukwuma Onuchukwu (C)

Federal Medical Centre, Keffi, Nigeria.

Huda Munir (H)

Aminu Kano Teaching Hospital, Kano, Nigeria.

Binta Wudil Jibir (BW)

Hasiya Bayero Paediatric Hospital, Kano, Nigeria.

Zubaida Farouk (Z)

Aminu Kano Teaching Hospital, Kano, Nigeria.

Safiya Gambo (S)

Murtala Muhammed Specialist Hospital, Kano, Nigeria.

Fatimah Hassan-Hanga (F)

Aminu Kano Teaching Hospital, Kano, Nigeria.

Rasaq Olaosebikan (R)

International Foundation Against Infectious Diseases in Nigeria, Abuja, Nigeria.

Bernard Ebruke (B)

International Foundation Against Infectious Diseases in Nigeria, Abuja, Nigeria.

Charles Esimone (C)

Nnamdi Azikiwe University, Awka, Nigeria.

Stephen Obaro (S)

Department of Pediatric Infectious Diseases, University of Nebraska Medical Center, Omaha, Nebraska, United States of America.

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