KRISHI
ICAR RESEARCH DATA REPOSITORY FOR KNOWLEDGE MANAGEMENT
(An Institutional Publication and Data Inventory Repository)
"Not Available": Please do not remove the default option "Not Available" for the fields where metadata information is not available
"1001-01-01": Date not available or not applicable for filling metadata infromation
"1001-01-01": Date not available or not applicable for filling metadata infromation
Please use this identifier to cite or link to this item:
http://krishi.icar.gov.in/jspui/handle/123456789/6949
Title: | Vancomycin analogue restores Meropenem activity against NDM-1 Gram negative pathogens |
Other Titles: | Not Available |
Authors: | Venkateswarlu Y Sarkar P Sandip S Manjunath GB Mitra SD Krishnamoorthy P Shome BR Haldar J |
ICAR Data Use Licennce: | http://krishi.icar.gov.in/PDF/ICAR_Data_Use_Licence.pdf |
Author's Affiliated institute: | Jawaharlal Nehru Centre for Advanced Scientific Research, Bengaluru ICAR::National Institute of Veterinary Epidemiology and Disease Informatics |
Published/ Complete Date: | 2018-05-04 |
Project Code: | Not Available |
Keywords: | antibacterial activity; antibiotic resistance; glycopeptide antibiotics; meropenem; NDM-1 Gram-negative bacteria; vancomycin |
Publisher: | American Chemical Society Publications |
Citation: | ACS Infect. Dis. 4, 7, 1093-1101 |
Series/Report no.: | Not Available; |
Abstract/Description: | New Delhi metallo-β-lactamase-1 (NDM-1) is the major contributor to the emergence of carbapenem resistance in Gram-negative pathogens (GNPs) and has caused many clinically available β-lactam antibiotics to become obsolete. A clinically approved inhibitor of metallo-β-lactamase (MBL) that could restore the activity of carbapenems against resistant GNPs has not yet been found, making NDM-1 a serious threat to human health. Here, we have rationally developed an inhibitor for the NDM-1 enzyme, which has the ability to penetrate the outer membrane of GNPs and inactivate the enzyme by depleting the metal ion (Zn2+) from the active site. The inhibitor reinstated the activity of meropenem against NDM-1 producing clinical isolates of GNPs like Klebsiella pneumoniae and Escherichia coli. Further, the inhibitor efficiently restored meropenem activity against NDM-1 producing K. pneumoniae in a murine sepsis infection model. These findings demonstrate that a combination of the present inhibitor and meropenem has high potential to be translated clinically to combat carbapenem-resistant GNPs. |
Description: | Not Available |
ISSN: | 2373-8227 |
Type(s) of content: | Research Paper |
Sponsors: | Not Available |
Language: | English |
Name of Journal: | ACS Infectious Diseases |
Volume No.: | 4(7) |
Page Number: | 1093-1101 |
Name of the Division/Regional Station: | Not Available |
Source, DOI or any other URL: | DOI: 10.1021/acsinfecdis.8b00011 |
URI: | http://krishi.icar.gov.in/jspui/handle/123456789/6949 |
Appears in Collections: | AS-NIVEDI-Publication |
Files in This Item:
There are no files associated with this item.
Items in KRISHI are protected by copyright, with all rights reserved, unless otherwise indicated.