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bla(CTX-M-I) group extended spectrum beta lactamase-producing Salmonella typhi from hospitalized patients in Lagos, Nigeria

PURPOSE: The global spread of bla(CTX-M-I) extended-spectrum beta-lactamase (ESBL)-producing Salmonella spp. remains a major threat to treatment and control. Evidence of emergence and spread of this marker are lacking in Nigeria. This study investigated bla(CTX-M-I) ESBL production among Salmonella...

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Autores principales: Akinyemi, Kabiru O, Iwalokun, Bamidele A, Alafe, Olajide O, Mudashiru, Sulaiman A, Fakorede, Christopher
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4437039/
https://www.ncbi.nlm.nih.gov/pubmed/25999745
http://dx.doi.org/10.2147/IDR.S78876
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author Akinyemi, Kabiru O
Iwalokun, Bamidele A
Alafe, Olajide O
Mudashiru, Sulaiman A
Fakorede, Christopher
author_facet Akinyemi, Kabiru O
Iwalokun, Bamidele A
Alafe, Olajide O
Mudashiru, Sulaiman A
Fakorede, Christopher
author_sort Akinyemi, Kabiru O
collection PubMed
description PURPOSE: The global spread of bla(CTX-M-I) extended-spectrum beta-lactamase (ESBL)-producing Salmonella spp. remains a major threat to treatment and control. Evidence of emergence and spread of this marker are lacking in Nigeria. This study investigated bla(CTX-M-I) ESBL production among Salmonella isolates from hospitalized patients. METHODS: Patients (158 total) made up of two groups were evaluated. Group A was composed of 135 patients with persistent pyrexia and group B was composed of 23 gastroenteritis patients and their stool samples. Samples were cultured, and isolates were identified and were subjected to antibiotic susceptibility testing by standard methods. Isolates were further screened for ESBL production, bla(CTX-M-I) genes and transferability by double disk synergy test, plasmid extraction, polymerase chain reaction, and conjugation experiment. RESULTS: Thirty-five (25.9%) Salmonella isolates were identified from group A, of which 74.3% were S. typhi, 22.9% were S. paratyphi and two (5.7%) were invasive non-typhoidal S. enteritidis. Nine Plasmodium falciparum infections were recorded, four of which were identified as co-infections with typhoidal Salmonella. Only two (8.7%) S. enteritidis samples were obtained from group B (P>0.05). A total of 24 isolates were ESBL-positive, eliciting resistance to five to seven antibiotics, and were multiple-drug resistant. ESBL production due to the bla(CTX-M-I) gene cluster was detected in eleven (45.8%) Salmonella isolates. Nine (81.8%) of the eleven bla(CTX-M-I) ESBL producers were S. typhi and two (18.2%) isolates were S. enteritidis. Four of nine S. typhi bla(CTX-M-I) ESBL-producing strains harbored 23 kb self-transmissible plasmid that was co-transferred with cefotaxime and augmentin resistance to Escherichia coli j53-2 transconjugants. CONCLUSION: This study revealed the emergence of bla(CTX-M-I) S. typhi as an agent of persistent pyrexia with potential to spread to other Enterobacteriaceae in Lagos, Nigeria. Cautionary prescription and judicious use of third-generation cephalosporins, particularly cefotaxime, for the treatment of typhoid fever and routine screening for P. falciparum co-infection with ESBL-producing Salmonella in the laboratories during diagnosis of persistent pyrexia conditions in patients are recommended.
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spelling pubmed-44370392015-05-21 bla(CTX-M-I) group extended spectrum beta lactamase-producing Salmonella typhi from hospitalized patients in Lagos, Nigeria Akinyemi, Kabiru O Iwalokun, Bamidele A Alafe, Olajide O Mudashiru, Sulaiman A Fakorede, Christopher Infect Drug Resist Original Research PURPOSE: The global spread of bla(CTX-M-I) extended-spectrum beta-lactamase (ESBL)-producing Salmonella spp. remains a major threat to treatment and control. Evidence of emergence and spread of this marker are lacking in Nigeria. This study investigated bla(CTX-M-I) ESBL production among Salmonella isolates from hospitalized patients. METHODS: Patients (158 total) made up of two groups were evaluated. Group A was composed of 135 patients with persistent pyrexia and group B was composed of 23 gastroenteritis patients and their stool samples. Samples were cultured, and isolates were identified and were subjected to antibiotic susceptibility testing by standard methods. Isolates were further screened for ESBL production, bla(CTX-M-I) genes and transferability by double disk synergy test, plasmid extraction, polymerase chain reaction, and conjugation experiment. RESULTS: Thirty-five (25.9%) Salmonella isolates were identified from group A, of which 74.3% were S. typhi, 22.9% were S. paratyphi and two (5.7%) were invasive non-typhoidal S. enteritidis. Nine Plasmodium falciparum infections were recorded, four of which were identified as co-infections with typhoidal Salmonella. Only two (8.7%) S. enteritidis samples were obtained from group B (P>0.05). A total of 24 isolates were ESBL-positive, eliciting resistance to five to seven antibiotics, and were multiple-drug resistant. ESBL production due to the bla(CTX-M-I) gene cluster was detected in eleven (45.8%) Salmonella isolates. Nine (81.8%) of the eleven bla(CTX-M-I) ESBL producers were S. typhi and two (18.2%) isolates were S. enteritidis. Four of nine S. typhi bla(CTX-M-I) ESBL-producing strains harbored 23 kb self-transmissible plasmid that was co-transferred with cefotaxime and augmentin resistance to Escherichia coli j53-2 transconjugants. CONCLUSION: This study revealed the emergence of bla(CTX-M-I) S. typhi as an agent of persistent pyrexia with potential to spread to other Enterobacteriaceae in Lagos, Nigeria. Cautionary prescription and judicious use of third-generation cephalosporins, particularly cefotaxime, for the treatment of typhoid fever and routine screening for P. falciparum co-infection with ESBL-producing Salmonella in the laboratories during diagnosis of persistent pyrexia conditions in patients are recommended. Dove Medical Press 2015-05-11 /pmc/articles/PMC4437039/ /pubmed/25999745 http://dx.doi.org/10.2147/IDR.S78876 Text en © 2015 Akinyemi et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Akinyemi, Kabiru O
Iwalokun, Bamidele A
Alafe, Olajide O
Mudashiru, Sulaiman A
Fakorede, Christopher
bla(CTX-M-I) group extended spectrum beta lactamase-producing Salmonella typhi from hospitalized patients in Lagos, Nigeria
title bla(CTX-M-I) group extended spectrum beta lactamase-producing Salmonella typhi from hospitalized patients in Lagos, Nigeria
title_full bla(CTX-M-I) group extended spectrum beta lactamase-producing Salmonella typhi from hospitalized patients in Lagos, Nigeria
title_fullStr bla(CTX-M-I) group extended spectrum beta lactamase-producing Salmonella typhi from hospitalized patients in Lagos, Nigeria
title_full_unstemmed bla(CTX-M-I) group extended spectrum beta lactamase-producing Salmonella typhi from hospitalized patients in Lagos, Nigeria
title_short bla(CTX-M-I) group extended spectrum beta lactamase-producing Salmonella typhi from hospitalized patients in Lagos, Nigeria
title_sort bla(ctx-m-i) group extended spectrum beta lactamase-producing salmonella typhi from hospitalized patients in lagos, nigeria
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4437039/
https://www.ncbi.nlm.nih.gov/pubmed/25999745
http://dx.doi.org/10.2147/IDR.S78876
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