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Published in: European Journal of Medical Research 1/2020

01-12-2020 | Ciprofloxacin | Research

A mechanistic approach to prove the efficacy of combination therapy against New Delhi metallo-β-lactamases producing bacterial strain: a molecular and biochemical approach

Authors: Lubna Maryam, Abid Ali, Shamsi Khalid, Asad U. Khan

Published in: European Journal of Medical Research | Issue 1/2020

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Abstract

Background

NDM-1 is a novel broad-spectrum metallo-β-lactamase with the capability to grant resistance to almost all β-lactam antibiotics. Its widespread dissemination made treatment options a major challenge to combat, causing threat to public health worldwide. Due to antibiotic resistance problems, development of effective therapeutics for infections caused by NDM-1 producing strains is urgently required. Since combination therapies are proved to be effective in many cases, this study was initiated to put forward novel effective antibiotics combinations for fighting infections caused by NDM-1 producing strains.

Methods

Streptomycin and amikacin combination and streptomycin and ciprofloxacin combination were tested by checkerboard assay. NDM-1 protein/enzyme was then expressed and purified to carry out enzyme kinetics study, CD and fluorescence spectroscopic studies.

Results

Streptomycin and amikacin combination and streptomycin and ciprofloxacin combination showed synergistic effect towards NDM-1 producing bacterial strains as shown by FICI results. NDM-1 producing bacterial cells were expressed and purified to obtain protein as the source of enzyme. When NDM-1 enzyme was treated with streptomycin along with amikacin, the efficiency of enzyme was decreased by 49.37% and when the enzyme was treated with streptomycin along with ciprofloxacin, the efficiency of enzyme was decreased by 29.66% as revealed by enzyme kinetic studies. Due to binding of streptomycin and amikacin in combination and streptomycin and ciprofloxacin in combination, conformational changes in the secondary structure of NDM-1 enzyme were observed by CD spectroscopic studies. Antibiotics streptomycin and ciprofloxacin bind with NDM-1 through exothermic processes, whereas amikacin binds through an endothermic process. All three antibiotics bind spontaneously with an association constant of the order of 104 M−1 as revealed by fluorescence spectroscopic studies.

Conclusions

The therapeutic combination of streptomycin with amikacin and ciprofloxacin plays an important role in inhibiting NDM-1 producing bacterial strains. Therefore, these combinations can be used as effective future therapeutic candidates against NDM-1 producing bacterial cells.
Literature
2.
go back to reference Queenan AM, Bush K. Carbapenemases: the versatile beta-lactamases. Clin Microbiol Rev. 2007;20(3):440–58.CrossRef Queenan AM, Bush K. Carbapenemases: the versatile beta-lactamases. Clin Microbiol Rev. 2007;20(3):440–58.CrossRef
6.
go back to reference Kummana C, Yuen K. Parenteral aminoglycoside therapy. Selection, administration and monitoring. Drugs. 1994;47:902–13.CrossRef Kummana C, Yuen K. Parenteral aminoglycoside therapy. Selection, administration and monitoring. Drugs. 1994;47:902–13.CrossRef
8.
go back to reference Mingeot-Leclercq MP, Glupczynski Y, Tulkens PM. Aminoglycosides: activity and resistance. Antimicrob Agents Chemother. 1999;43(4):727–37.CrossRef Mingeot-Leclercq MP, Glupczynski Y, Tulkens PM. Aminoglycosides: activity and resistance. Antimicrob Agents Chemother. 1999;43(4):727–37.CrossRef
10.
go back to reference King DE, Malone R, Lilley SH. New classification and update on the quinolone antibiotics. Am Fam Physician. 2000;61(9):2741–8.PubMed King DE, Malone R, Lilley SH. New classification and update on the quinolone antibiotics. Am Fam Physician. 2000;61(9):2741–8.PubMed
12.
go back to reference Hooper DC. Emerging mechanisms of fluoroquinolone resistance. Emerg Infect Dis. 2001;7(2):337.CrossRef Hooper DC. Emerging mechanisms of fluoroquinolone resistance. Emerg Infect Dis. 2001;7(2):337.CrossRef
13.
go back to reference Berdal JE, Skra I, Mowinckel P, Gulbrandsen P, Bjørnholt JV. Use of rifampicin and ciprofloxacin combination therapy after surgical debridement in the treatment of early manifestation prosthetic joint infections. Clin Microbiol Infect. 2005;11(10):843–5.CrossRef Berdal JE, Skra I, Mowinckel P, Gulbrandsen P, Bjørnholt JV. Use of rifampicin and ciprofloxacin combination therapy after surgical debridement in the treatment of early manifestation prosthetic joint infections. Clin Microbiol Infect. 2005;11(10):843–5.CrossRef
14.
go back to reference Liu H, Mulholland SG. Appropriate antibiotic treatment of genitourinary infections in hospitalized patients. Am J Med. 2005;118(7):14–20.CrossRef Liu H, Mulholland SG. Appropriate antibiotic treatment of genitourinary infections in hospitalized patients. Am J Med. 2005;118(7):14–20.CrossRef
25.
go back to reference Wayne PA. Performance standards for antimicrobial susceptibility testing: 21st informational supplement. Clinical and Laboratory Standards Institute. 2011; M100-S21. Wayne PA. Performance standards for antimicrobial susceptibility testing: 21st informational supplement. Clinical and Laboratory Standards Institute. 2011; M100-S21.
27.
go back to reference Galleni M, Franceschini N, Quinting B, Fattorini L, Orefici G, Oratore A, Frère JM, Amicosante G. Use of the chromosomal class A beta-lactamase of Mycobacterium fortuitum D316 to study potentially poor substrates and inhibitory beta-lactam compounds. Antimicrob Agents Chemother. 1994;38(7):1608–14.CrossRef Galleni M, Franceschini N, Quinting B, Fattorini L, Orefici G, Oratore A, Frère JM, Amicosante G. Use of the chromosomal class A beta-lactamase of Mycobacterium fortuitum D316 to study potentially poor substrates and inhibitory beta-lactam compounds. Antimicrob Agents Chemother. 1994;38(7):1608–14.CrossRef
33.
go back to reference Kang J, Liu Y, Xie MX, Li S, Jiang M, Wang YD. Interactions of human serum albumin with chlorogenic acid and ferulic acid. Biochem Biophys Acta. 2004;1674(2):205–14.CrossRef Kang J, Liu Y, Xie MX, Li S, Jiang M, Wang YD. Interactions of human serum albumin with chlorogenic acid and ferulic acid. Biochem Biophys Acta. 2004;1674(2):205–14.CrossRef
35.
go back to reference O’Callaghan CH, Morris A, Kirby SM, Shingler AH. Novel method for detection of β-lactamases by using a chromogenic cephalosporin substrate. Antimicrob Agents Chemother. 1972;1(4):283–8.CrossRef O’Callaghan CH, Morris A, Kirby SM, Shingler AH. Novel method for detection of β-lactamases by using a chromogenic cephalosporin substrate. Antimicrob Agents Chemother. 1972;1(4):283–8.CrossRef
36.
go back to reference Croney JC, Jameson DM, Learmonth RP. Fluorescence spectroscopy in biochemistry: teaching basic principles with visual demonstrations. Biochem Mol Biol Educ. 2001;29(2):60–5.CrossRef Croney JC, Jameson DM, Learmonth RP. Fluorescence spectroscopy in biochemistry: teaching basic principles with visual demonstrations. Biochem Mol Biol Educ. 2001;29(2):60–5.CrossRef
37.
go back to reference Möller M, Denicola A. Protein tryptophan accessibility studied by fluorescence quenching. Biochem Mol Biol Educ. 2002;30(3):175–8.CrossRef Möller M, Denicola A. Protein tryptophan accessibility studied by fluorescence quenching. Biochem Mol Biol Educ. 2002;30(3):175–8.CrossRef
38.
go back to reference Eftink MR, Ghiron CA. Exposure of tryptophanyl residues in proteins. Quantitative determination by fluorescence quenching studies. Biochemistry. 1976;15(3):672–80.CrossRef Eftink MR, Ghiron CA. Exposure of tryptophanyl residues in proteins. Quantitative determination by fluorescence quenching studies. Biochemistry. 1976;15(3):672–80.CrossRef
39.
go back to reference Lakowicz JR. Principles of frequency-domain fluorescence spectroscopy and applications to cell membranes. In: Fluorescence studies on biological membranes. Boston: Springer; 1988, p. 89–126. Lakowicz JR. Principles of frequency-domain fluorescence spectroscopy and applications to cell membranes. In: Fluorescence studies on biological membranes. Boston: Springer; 1988, p. 89–126.
41.
go back to reference Maryam L, Khalid S, Ali A, Khan AU. Significant role of Asn-247 and Arg-64 residues in close proximity of the active site in maintaining the catalytic function of CTX-M-15 type β-lactamase. RSC Adv. 2019;9(10):5325–37.CrossRef Maryam L, Khalid S, Ali A, Khan AU. Significant role of Asn-247 and Arg-64 residues in close proximity of the active site in maintaining the catalytic function of CTX-M-15 type β-lactamase. RSC Adv. 2019;9(10):5325–37.CrossRef
42.
go back to reference Michalak K, Sobolewska-Włodarczyk A, Włodarczyk M, Sobolewska J, Woźniak P, Sobolewski B. Treatment of the fluoroquinolone-associated disability: the pathobiochemical implications. Oxid Med Cell Longev. 2017;2017:8023935.PubMedPubMedCentral Michalak K, Sobolewska-Włodarczyk A, Włodarczyk M, Sobolewska J, Woźniak P, Sobolewski B. Treatment of the fluoroquinolone-associated disability: the pathobiochemical implications. Oxid Med Cell Longev. 2017;2017:8023935.PubMedPubMedCentral
Metadata
Title
A mechanistic approach to prove the efficacy of combination therapy against New Delhi metallo-β-lactamases producing bacterial strain: a molecular and biochemical approach
Authors
Lubna Maryam
Abid Ali
Shamsi Khalid
Asad U. Khan
Publication date
01-12-2020
Publisher
BioMed Central
Published in
European Journal of Medical Research / Issue 1/2020
Electronic ISSN: 2047-783X
DOI
https://doi.org/10.1186/s40001-020-00418-1

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