Changing paradigm of antibiotic resistance amongst Escherichia coli isolates in Indian pediatric population

Antimicrobial resistance happens when microorganisms mutates in manners that render the drugs like antibacterial, antiviral, antiparasitic and antifungal, ineffective. The normal mutation process is encouraged by the improper use of antibiotics. Mutations leading to quinolone resistance occur in a h...

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Published inPloS one Vol. 14; no. 4; p. e0213850
Main Authors Singh, Taru, Singh, Praveen Kumar, Dar, Sajad Ahmad, Haque, Shafiul, Akhter, Naseem, Das, Shukla
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 17.04.2019
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Abstract Antimicrobial resistance happens when microorganisms mutates in manners that render the drugs like antibacterial, antiviral, antiparasitic and antifungal, ineffective. The normal mutation process is encouraged by the improper use of antibiotics. Mutations leading to quinolone resistance occur in a highly conserved region of the quinolone resistance-determining region (QRDR) of DNA gyrAse and topoisomerase IV gene. We analyzed antibiotic resistant genes and single nucleotide polymorphism (SNP) in gyrA and parC genes in QRDR in 120 E. coli isolates (both diarrheagenic and non-pathogenic) recovered from fresh stool samples collected from children aged less than 5 years from Delhi, India. Antibiotic susceptibility testing was performed according to standard clinical and laboratory standards institute (CLSI) guidelines. Phylogenetic analysis showed the clonal diversity and phylogenetic relationships among the E. coli isolates. The SNP analysis depicted mutations in gyrA and parC genes in QRDR. The sul1 gene, responsible for sulfonamide resistance, was present in almost half (47.5%) of the isolates across the diseased and healthy samples. The presence of antibiotic resistance genes in E. coli isolates from healthy children indicate the development, dissemination and carriage of antibiotic resistance in their gut. Our observations suggest the implementation of active surveillance and stewardship programs to promote appropriate antibiotic use and minimizing further danger.
AbstractList Antimicrobial resistance happens when microorganisms mutates in manners that render the drugs like antibacterial, antiviral, antiparasitic and antifungal, ineffective. The normal mutation process is encouraged by the improper use of antibiotics. Mutations leading to quinolone resistance occur in a highly conserved region of the quinolone resistance-determining region (QRDR) of DNA gyrAse and topoisomerase IV gene. We analyzed antibiotic resistant genes and single nucleotide polymorphism (SNP) in gyrA and parC genes in QRDR in 120 E. coli isolates (both diarrheagenic and non-pathogenic) recovered from fresh stool samples collected from children aged less than 5 years from Delhi, India. Antibiotic susceptibility testing was performed according to standard clinical and laboratory standards institute (CLSI) guidelines. Phylogenetic analysis showed the clonal diversity and phylogenetic relationships among the E. coli isolates. The SNP analysis depicted mutations in gyrA and parC genes in QRDR. The sul1 gene, responsible for sulfonamide resistance, was present in almost half (47.5%) of the isolates across the diseased and healthy samples. The presence of antibiotic resistance genes in E. coli isolates from healthy children indicate the development, dissemination and carriage of antibiotic resistance in their gut. Our observations suggest the implementation of active surveillance and stewardship programs to promote appropriate antibiotic use and minimizing further danger.
Antimicrobial resistance happens when microorganisms mutates in manners that render the drugs like antibacterial, antiviral, antiparasitic and antifungal, ineffective. The normal mutation process is encouraged by the improper use of antibiotics. Mutations leading to quinolone resistance occur in a highly conserved region of the quinolone resistance-determining region (QRDR) of DNA gyrA se and topoisomerase IV gene. We analyzed antibiotic resistant genes and single nucleotide polymorphism (SNP) in gyrA and parC genes in QRDR in 120 E . coli isolates (both diarrheagenic and non-pathogenic) recovered from fresh stool samples collected from children aged less than 5 years from Delhi, India. Antibiotic susceptibility testing was performed according to standard clinical and laboratory standards institute (CLSI) guidelines. Phylogenetic analysis showed the clonal diversity and phylogenetic relationships among the E . coli isolates. The SNP analysis depicted mutations in gyrA and parC genes in QRDR. The sul1 gene, responsible for sulfonamide resistance, was present in almost half (47.5%) of the isolates across the diseased and healthy samples. The presence of antibiotic resistance genes in E . coli isolates from healthy children indicate the development, dissemination and carriage of antibiotic resistance in their gut. Our observations suggest the implementation of active surveillance and stewardship programs to promote appropriate antibiotic use and minimizing further danger.
Audience Academic
Author Akhter, Naseem
Singh, Taru
Das, Shukla
Haque, Shafiul
Singh, Praveen Kumar
Dar, Sajad Ahmad
AuthorAffiliation 2 Research and Scientific Studies Unit, College of Nursing and Allied Health Sciences, Jazan University, Jazan, Saudi Arabia
1 Department of Microbiology, University College of Medical Sciences & GTB Hospital (University of Delhi), Delhi, India
3 Department of Laboratory Medicine, Faculty of Applied Medical Sciences, Albaha University, Albaha, Saudi Arabia
Tallinn University of Technology, ESTONIA
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2019 Singh et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
2019 Singh et al 2019 Singh et al
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– notice: 2019 Singh et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
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Snippet Antimicrobial resistance happens when microorganisms mutates in manners that render the drugs like antibacterial, antiviral, antiparasitic and antifungal,...
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StartPage e0213850
SubjectTerms Antibacterial agents
Antibiotic resistance
Antibiotics
Antifungal agents
Antiinfectives and antibacterials
Antimicrobial agents
Antimicrobial resistance
Antiviral agents
Biology and Life Sciences
Care and treatment
Child, Preschool
Childhood diarrhea
Children
Deoxyribonucleic acid
DNA
DNA topoisomerase
DNA topoisomerase IV
Drug resistance
Drug Resistance, Bacterial - genetics
E coli
Escherichia coli
Escherichia coli - genetics
Escherichia coli - isolation & purification
Escherichia coli Infections - genetics
Escherichia coli Proteins - genetics
Female
Fungicides
Gene polymorphism
Genes
Genetic aspects
Genetic polymorphisms
Hazards
Health aspects
Health sciences
Hospitals
Humans
India
Infant
Infant, Newborn
Infections
Male
Medicine and Health Sciences
Microbial drug resistance
Microorganisms
Mutation
Patient outcomes
Pediatrics
Phylogenetics
Phylogeny
Plasmids
Polymorphism
Polymorphism, Single Nucleotide
Research and Analysis Methods
Risk factors
Single nucleotide polymorphisms
Single-nucleotide polymorphism
Studies
Sul1 gene
Sulfonamides
Surveillance
Tetracyclines
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Title Changing paradigm of antibiotic resistance amongst Escherichia coli isolates in Indian pediatric population
URI https://www.ncbi.nlm.nih.gov/pubmed/30995225
https://www.proquest.com/docview/2210979368
https://search.proquest.com/docview/2211327465
https://pubmed.ncbi.nlm.nih.gov/PMC6469777
https://doaj.org/article/017d5185044a43efb4e5d1fe8a5291c7
http://dx.doi.org/10.1371/journal.pone.0213850
Volume 14
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