Cargando…
1373. Activity of Ceftriaxone–Sulbactam–EDTA Against Multi-Drug-resistant A. baumannii, P. aeruginosa and Enterobacteriaceae Isolates (WHO Critical Priority Pathogens) Collected from Various Hospitals in India
BACKGROUND: Ceftriaxone–Sulbactam–EDTA (CSE) is the first cephalosporin–β-lactamase inhibitor combination with an antibiotic resistance breaker–disodium edetate, recently evaluated in a Phase 3 clinical trial for treatment of adults with complicated urinary tract infections (NCT03477422). The additi...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6252651/ http://dx.doi.org/10.1093/ofid/ofy210.1204 |
_version_ | 1783373312489947136 |
---|---|
author | Girotra, Ruchi Pyasi, Anurag Chaudhary, Manu Patil, N S Mir, Mohd Amin Chaudhary, Saransh Mandale, Pankaj |
author_facet | Girotra, Ruchi Pyasi, Anurag Chaudhary, Manu Patil, N S Mir, Mohd Amin Chaudhary, Saransh Mandale, Pankaj |
author_sort | Girotra, Ruchi |
collection | PubMed |
description | BACKGROUND: Ceftriaxone–Sulbactam–EDTA (CSE) is the first cephalosporin–β-lactamase inhibitor combination with an antibiotic resistance breaker–disodium edetate, recently evaluated in a Phase 3 clinical trial for treatment of adults with complicated urinary tract infections (NCT03477422). The addition of Sulbactam and EDTA expands the spectrum of activity of Ceftriaxone to include extended-spectrum-β-lactamase (ESBL) and metallo-β-lactamase (MBL) producing bacteria. This study evaluated the in vitro activity of CSE against 3,150 isolates (716 (22.73%) E. coli; 435 (13.81%) K. pneumoniae; 1,075 (34.13%) A. baumannii; 924 (29.33%) P. aeruginosa) collected from 22 hospitals in India during 2013–2016. METHODS: A total of 3,150 nonduplicate Gram-negative clinical isolates were collected, and susceptibility testing was conducted using reference broth microdilution method for CSE and comparators. CLSI defined phenotypic methods were used for ESBL and MBL detection, and thereafter, all isolates were further characterized genotypically using single PCRs and a panel of primers for detection of most β-lactamase enzymes, including bla(TEM), bla(SHV), bla(CTX-M), bla(AmpC), bla(OXA), bla(KPC), bla(VIM), bla(NDM), and bla(IMP). RESULTS: Of the 3,150 isolates, 2,717 (86.25%) were β-lactamase producers, of which, 851 (31.32%) tested positive for ESBL, 1,591 (58.56%) tested positive for MBL, while 275 (10.12%) tested positive for both ESBL and MBL production during phenotypic evaluation. Once the genotype data were available, isolates were re-characterized as per the functional classification of β-lactamases into four distinct categories, including ESBL, AmpC, Carbapenemase and MBL. An astonishing 1,866 (59.23%) isolates harbored at least one MBL gene, of which, the prevalence was the highest in A. baumannii (78.6%), followed by K. pneumoniae (63%), P. aeruginosa (46.6%) and E. coli (44.1%). A summary of the results of susceptibility testing is shown in Figures 1, 2, and 3. [Image: see text] [Image: see text] [Image: see text] CONCLUSION: CSE showed a high overall susceptibility in ESBL- and MBL-producing bacteria and could provide a useful alternative to carbapenems and colistin in clinical settings. DISCLOSURES: R. Girotra, Venus Medicine Research Centre: Employee, Salary. A. Pyasi, Venus Medicine Research Centre: Employee, Salary. M. Chaudhary, Venus Medicine Research Centre: Board Member and Shareholder, Salary. M. A. Mir, Venus Medicine Research Centre: Employee, Salary. S. Chaudhary, Venus Medicine Research Centre: Employee and Shareholder, Salary. P. Mandale, Venus Medicine Research Centre: Employee, Salary. |
format | Online Article Text |
id | pubmed-6252651 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-62526512018-11-28 1373. Activity of Ceftriaxone–Sulbactam–EDTA Against Multi-Drug-resistant A. baumannii, P. aeruginosa and Enterobacteriaceae Isolates (WHO Critical Priority Pathogens) Collected from Various Hospitals in India Girotra, Ruchi Pyasi, Anurag Chaudhary, Manu Patil, N S Mir, Mohd Amin Chaudhary, Saransh Mandale, Pankaj Open Forum Infect Dis Abstracts BACKGROUND: Ceftriaxone–Sulbactam–EDTA (CSE) is the first cephalosporin–β-lactamase inhibitor combination with an antibiotic resistance breaker–disodium edetate, recently evaluated in a Phase 3 clinical trial for treatment of adults with complicated urinary tract infections (NCT03477422). The addition of Sulbactam and EDTA expands the spectrum of activity of Ceftriaxone to include extended-spectrum-β-lactamase (ESBL) and metallo-β-lactamase (MBL) producing bacteria. This study evaluated the in vitro activity of CSE against 3,150 isolates (716 (22.73%) E. coli; 435 (13.81%) K. pneumoniae; 1,075 (34.13%) A. baumannii; 924 (29.33%) P. aeruginosa) collected from 22 hospitals in India during 2013–2016. METHODS: A total of 3,150 nonduplicate Gram-negative clinical isolates were collected, and susceptibility testing was conducted using reference broth microdilution method for CSE and comparators. CLSI defined phenotypic methods were used for ESBL and MBL detection, and thereafter, all isolates were further characterized genotypically using single PCRs and a panel of primers for detection of most β-lactamase enzymes, including bla(TEM), bla(SHV), bla(CTX-M), bla(AmpC), bla(OXA), bla(KPC), bla(VIM), bla(NDM), and bla(IMP). RESULTS: Of the 3,150 isolates, 2,717 (86.25%) were β-lactamase producers, of which, 851 (31.32%) tested positive for ESBL, 1,591 (58.56%) tested positive for MBL, while 275 (10.12%) tested positive for both ESBL and MBL production during phenotypic evaluation. Once the genotype data were available, isolates were re-characterized as per the functional classification of β-lactamases into four distinct categories, including ESBL, AmpC, Carbapenemase and MBL. An astonishing 1,866 (59.23%) isolates harbored at least one MBL gene, of which, the prevalence was the highest in A. baumannii (78.6%), followed by K. pneumoniae (63%), P. aeruginosa (46.6%) and E. coli (44.1%). A summary of the results of susceptibility testing is shown in Figures 1, 2, and 3. [Image: see text] [Image: see text] [Image: see text] CONCLUSION: CSE showed a high overall susceptibility in ESBL- and MBL-producing bacteria and could provide a useful alternative to carbapenems and colistin in clinical settings. DISCLOSURES: R. Girotra, Venus Medicine Research Centre: Employee, Salary. A. Pyasi, Venus Medicine Research Centre: Employee, Salary. M. Chaudhary, Venus Medicine Research Centre: Board Member and Shareholder, Salary. M. A. Mir, Venus Medicine Research Centre: Employee, Salary. S. Chaudhary, Venus Medicine Research Centre: Employee and Shareholder, Salary. P. Mandale, Venus Medicine Research Centre: Employee, Salary. Oxford University Press 2018-11-26 /pmc/articles/PMC6252651/ http://dx.doi.org/10.1093/ofid/ofy210.1204 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Abstracts Girotra, Ruchi Pyasi, Anurag Chaudhary, Manu Patil, N S Mir, Mohd Amin Chaudhary, Saransh Mandale, Pankaj 1373. Activity of Ceftriaxone–Sulbactam–EDTA Against Multi-Drug-resistant A. baumannii, P. aeruginosa and Enterobacteriaceae Isolates (WHO Critical Priority Pathogens) Collected from Various Hospitals in India |
title | 1373. Activity of Ceftriaxone–Sulbactam–EDTA Against Multi-Drug-resistant A. baumannii, P. aeruginosa and Enterobacteriaceae Isolates (WHO Critical Priority Pathogens) Collected from Various Hospitals in India |
title_full | 1373. Activity of Ceftriaxone–Sulbactam–EDTA Against Multi-Drug-resistant A. baumannii, P. aeruginosa and Enterobacteriaceae Isolates (WHO Critical Priority Pathogens) Collected from Various Hospitals in India |
title_fullStr | 1373. Activity of Ceftriaxone–Sulbactam–EDTA Against Multi-Drug-resistant A. baumannii, P. aeruginosa and Enterobacteriaceae Isolates (WHO Critical Priority Pathogens) Collected from Various Hospitals in India |
title_full_unstemmed | 1373. Activity of Ceftriaxone–Sulbactam–EDTA Against Multi-Drug-resistant A. baumannii, P. aeruginosa and Enterobacteriaceae Isolates (WHO Critical Priority Pathogens) Collected from Various Hospitals in India |
title_short | 1373. Activity of Ceftriaxone–Sulbactam–EDTA Against Multi-Drug-resistant A. baumannii, P. aeruginosa and Enterobacteriaceae Isolates (WHO Critical Priority Pathogens) Collected from Various Hospitals in India |
title_sort | 1373. activity of ceftriaxone–sulbactam–edta against multi-drug-resistant a. baumannii, p. aeruginosa and enterobacteriaceae isolates (who critical priority pathogens) collected from various hospitals in india |
topic | Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6252651/ http://dx.doi.org/10.1093/ofid/ofy210.1204 |
work_keys_str_mv | AT girotraruchi 1373activityofceftriaxonesulbactamedtaagainstmultidrugresistantabaumanniipaeruginosaandenterobacteriaceaeisolateswhocriticalprioritypathogenscollectedfromvarioushospitalsinindia AT pyasianurag 1373activityofceftriaxonesulbactamedtaagainstmultidrugresistantabaumanniipaeruginosaandenterobacteriaceaeisolateswhocriticalprioritypathogenscollectedfromvarioushospitalsinindia AT chaudharymanu 1373activityofceftriaxonesulbactamedtaagainstmultidrugresistantabaumanniipaeruginosaandenterobacteriaceaeisolateswhocriticalprioritypathogenscollectedfromvarioushospitalsinindia AT patilns 1373activityofceftriaxonesulbactamedtaagainstmultidrugresistantabaumanniipaeruginosaandenterobacteriaceaeisolateswhocriticalprioritypathogenscollectedfromvarioushospitalsinindia AT mirmohdamin 1373activityofceftriaxonesulbactamedtaagainstmultidrugresistantabaumanniipaeruginosaandenterobacteriaceaeisolateswhocriticalprioritypathogenscollectedfromvarioushospitalsinindia AT chaudharysaransh 1373activityofceftriaxonesulbactamedtaagainstmultidrugresistantabaumanniipaeruginosaandenterobacteriaceaeisolateswhocriticalprioritypathogenscollectedfromvarioushospitalsinindia AT mandalepankaj 1373activityofceftriaxonesulbactamedtaagainstmultidrugresistantabaumanniipaeruginosaandenterobacteriaceaeisolateswhocriticalprioritypathogenscollectedfromvarioushospitalsinindia AT 1373activityofceftriaxonesulbactamedtaagainstmultidrugresistantabaumanniipaeruginosaandenterobacteriaceaeisolateswhocriticalprioritypathogenscollectedfromvarioushospitalsinindia |