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Community acquisition of β-lactamase producing Enterobacteriaceae in neonatal gut

BACKGROUND: Commensal flora constitutes a reservoir of antibiotic resistance. The increasing variety of β-lactamases and the emergence of Carbapenem resistant Enterobacteriaceae (CRE) in community, raise concerns regarding efficacy of β-lactams. It is important to know the exact load of antibiotic r...

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Autores principales: Kothari, Charu, Gaind, Rajni, Singh, Laishram Chandreshwor, Sinha, Anju, Kumari, Vidya, Arya, Sugandha, Chellani, Harish, Saxena, Sunita, Deb, Monorama
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3689095/
https://www.ncbi.nlm.nih.gov/pubmed/23773627
http://dx.doi.org/10.1186/1471-2180-13-136
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author Kothari, Charu
Gaind, Rajni
Singh, Laishram Chandreshwor
Sinha, Anju
Kumari, Vidya
Arya, Sugandha
Chellani, Harish
Saxena, Sunita
Deb, Monorama
author_facet Kothari, Charu
Gaind, Rajni
Singh, Laishram Chandreshwor
Sinha, Anju
Kumari, Vidya
Arya, Sugandha
Chellani, Harish
Saxena, Sunita
Deb, Monorama
author_sort Kothari, Charu
collection PubMed
description BACKGROUND: Commensal flora constitutes a reservoir of antibiotic resistance. The increasing variety of β-lactamases and the emergence of Carbapenem resistant Enterobacteriaceae (CRE) in community, raise concerns regarding efficacy of β-lactams. It is important to know the exact load of antibiotic resistance in the absence of any antibiotic selection pressure including via food and water. In the present study gut colonization in neonates with no direct antibiotic pressure was used as a model to evaluate β-lactam resistance in the community. RESULTS: In this prospective study, 75 healthy, vaginally delivered, antibiotic naive, breast fed neonates were studied for gut colonization by Extended spectrum β-lactamases (ESBL), AmpC β-lactamases hyperproducing Enterobacteriaceae and CRE on day 0, 21 and 60. Total 267 Enterobacteriaceae were isolated and E.coli was the predominant flora. ESBL, AmpC and coproduction was seen in 20.6%, 19.9% and 11.2% isolates respectively. ESBL carriage increased threefold from day 1 to 60 showing predominance of CTX-M group 15 (82.5%), ampC genes were heterogeneous. Colonization with CRE was rare, only one baby harboured Enterobacter sp positive for kpc-2. The reservoirs for these genes are likely to be mother and the environment. CONCLUSIONS: Data strongly suggests that in absence of any antibiotic pressure there is tremendous load of antibiotic resistance to β-lactam drugs. Wide spread presence of ESBL and AmpC can drive rapid emergence and dissemination of CRE. This is the first report from India which depicts the smaller picture of true antibiotic pressure present in the Indian community.
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spelling pubmed-36890952013-06-22 Community acquisition of β-lactamase producing Enterobacteriaceae in neonatal gut Kothari, Charu Gaind, Rajni Singh, Laishram Chandreshwor Sinha, Anju Kumari, Vidya Arya, Sugandha Chellani, Harish Saxena, Sunita Deb, Monorama BMC Microbiol Research Article BACKGROUND: Commensal flora constitutes a reservoir of antibiotic resistance. The increasing variety of β-lactamases and the emergence of Carbapenem resistant Enterobacteriaceae (CRE) in community, raise concerns regarding efficacy of β-lactams. It is important to know the exact load of antibiotic resistance in the absence of any antibiotic selection pressure including via food and water. In the present study gut colonization in neonates with no direct antibiotic pressure was used as a model to evaluate β-lactam resistance in the community. RESULTS: In this prospective study, 75 healthy, vaginally delivered, antibiotic naive, breast fed neonates were studied for gut colonization by Extended spectrum β-lactamases (ESBL), AmpC β-lactamases hyperproducing Enterobacteriaceae and CRE on day 0, 21 and 60. Total 267 Enterobacteriaceae were isolated and E.coli was the predominant flora. ESBL, AmpC and coproduction was seen in 20.6%, 19.9% and 11.2% isolates respectively. ESBL carriage increased threefold from day 1 to 60 showing predominance of CTX-M group 15 (82.5%), ampC genes were heterogeneous. Colonization with CRE was rare, only one baby harboured Enterobacter sp positive for kpc-2. The reservoirs for these genes are likely to be mother and the environment. CONCLUSIONS: Data strongly suggests that in absence of any antibiotic pressure there is tremendous load of antibiotic resistance to β-lactam drugs. Wide spread presence of ESBL and AmpC can drive rapid emergence and dissemination of CRE. This is the first report from India which depicts the smaller picture of true antibiotic pressure present in the Indian community. BioMed Central 2013-06-17 /pmc/articles/PMC3689095/ /pubmed/23773627 http://dx.doi.org/10.1186/1471-2180-13-136 Text en Copyright © 2013 Kothari et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Kothari, Charu
Gaind, Rajni
Singh, Laishram Chandreshwor
Sinha, Anju
Kumari, Vidya
Arya, Sugandha
Chellani, Harish
Saxena, Sunita
Deb, Monorama
Community acquisition of β-lactamase producing Enterobacteriaceae in neonatal gut
title Community acquisition of β-lactamase producing Enterobacteriaceae in neonatal gut
title_full Community acquisition of β-lactamase producing Enterobacteriaceae in neonatal gut
title_fullStr Community acquisition of β-lactamase producing Enterobacteriaceae in neonatal gut
title_full_unstemmed Community acquisition of β-lactamase producing Enterobacteriaceae in neonatal gut
title_short Community acquisition of β-lactamase producing Enterobacteriaceae in neonatal gut
title_sort community acquisition of β-lactamase producing enterobacteriaceae in neonatal gut
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3689095/
https://www.ncbi.nlm.nih.gov/pubmed/23773627
http://dx.doi.org/10.1186/1471-2180-13-136
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