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 in | PloS one Vol. 14; no. 4; p. e0213850 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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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. |
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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 |
AuthorAffiliation_xml | – name: 1 Department of Microbiology, University College of Medical Sciences & GTB Hospital (University of Delhi), Delhi, India – name: 3 Department of Laboratory Medicine, Faculty of Applied Medical Sciences, Albaha University, Albaha, Saudi Arabia – name: Tallinn University of Technology, ESTONIA – name: 2 Research and Scientific Studies Unit, College of Nursing and Allied Health Sciences, Jazan University, Jazan, Saudi Arabia |
Author_xml | – sequence: 1 givenname: Taru orcidid: 0000-0002-8117-2423 surname: Singh fullname: Singh, Taru organization: Department of Microbiology, University College of Medical Sciences & GTB Hospital (University of Delhi), Delhi, India – sequence: 2 givenname: Praveen Kumar orcidid: 0000-0003-2429-7913 surname: Singh fullname: Singh, Praveen Kumar organization: Department of Microbiology, University College of Medical Sciences & GTB Hospital (University of Delhi), Delhi, India – sequence: 3 givenname: Sajad Ahmad surname: Dar fullname: Dar, Sajad Ahmad organization: Research and Scientific Studies Unit, College of Nursing and Allied Health Sciences, Jazan University, Jazan, Saudi Arabia – sequence: 4 givenname: Shafiul surname: Haque fullname: Haque, Shafiul organization: Research and Scientific Studies Unit, College of Nursing and Allied Health Sciences, Jazan University, Jazan, Saudi Arabia – sequence: 5 givenname: Naseem surname: Akhter fullname: Akhter, Naseem organization: Department of Laboratory Medicine, Faculty of Applied Medical Sciences, Albaha University, Albaha, Saudi Arabia – sequence: 6 givenname: Shukla surname: Das fullname: Das, Shukla organization: Department of Microbiology, University College of Medical Sciences & GTB Hospital (University of Delhi), Delhi, India |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/30995225$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1016_j_micpath_2020_104680 crossref_primary_10_1080_1040841X_2022_2080525 crossref_primary_10_3390_antibiotics11101333 crossref_primary_10_1038_s41598_021_02251_w crossref_primary_10_1016_j_scitotenv_2021_148047 crossref_primary_10_1007_s11270_021_05440_5 crossref_primary_10_1177_17571774241239780 crossref_primary_10_56083_RCV3N12_268 |
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Copyright | COPYRIGHT 2019 Public Library of Science 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 |
Copyright_xml | – notice: COPYRIGHT 2019 Public Library of Science – 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. – notice: 2019 Singh et al 2019 Singh et al |
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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 |
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