In vitro effects of quinine on the antibacterial activity of erythromycin against bacteria of clinical relevance

Authors

  • Oluremi Adejoke Akinwale Department of Microbiology, School of Science and Technology, PMB 4005, Babcock University, Ilisan-Remo, Ogun State, Nigeria.
  • Uyi Oluwatobi Emokpae Department of Microbiology, School of Science and Technology, PMB 4005, Babcock University, Ilisan-Remo, Ogun State, Nigeria.
  • Opeyemi Mariam Adebogun Department of Microbiology, School of Science and Technology, PMB 4005, Babcock University, Ilisan-Remo, Ogun State, Nigeria.
  • Morenike Olutumbi Adeoye-Isijola Department of Microbiology, School of Science and Technology, PMB 4005, Babcock University, Ilisan-Remo, Ogun State, Nigeria.
  • Olufunmiso Olusola Olajuyigbe Department of Microbiology, School of Science and Technology, PMB 4005, Babcock University, Ilisan-Remo, Ogun State, Nigeria.

DOI:

https://doi.org/10.30574/gscbps.2021.14.2.0033

Keywords:

Antibacterial combination, Erythromycin, Resistance, Synergism, Quinine

Abstract

The study investigated the in vitro effects of quinine on the antibacterial activity of erythromycin for possible interactions. The antibacterial activities of each drug and their combinations were investigated by agar diffusion, agar and macrobroth dilution methods. While 100 µl of 1000 µg/ml of erythromycin produced inhibition zones ranging between 13 and 31 ± 1.0 mm in all the isolates except K. pneumoniae and P. aeruginosa ATCC 19582, combining the highest concentration of erythromycin with 35 µg/ml of quinine produced inhibition zones ranging between 14 and 34 ± 1.0 mm with the exception of S. flexneri KZN. Though quinine had no antibacterial effects on the isolates, erythromycin was effective at minimum inhibitory concentrations (MICs) ranging between 25 and 100 µg/ml while their combinations resulted in reduction of MICs of most of the isolates to 12.5 µg/ml except those against A. calcaoceuticus anitratus CSIR, Ps. aeruginosa ATCC 15442, P. shigelloides ATCC 51903, A. hydrophila ATCC 35654, Ps. aeruginosa ATCC 19582 and E. faecalis KZN that remained unchanged in agar dilution. While the MICs of erythromycin ranged between 25 and 50 µg/ml, the MICs of this antibiotic was reduced to concentrations ranging between 12.5 and 50 µg/ml indicating 50% to 75% in the presence of quinine. The combination of erythromycin and quinine, in vitro, resulted in synergistic (50%), additive/indifference (44.44%) and antagonistic (11.11%) interactions while quinine at concentrations lower than plasma quinine concentrations was inhibitory to the antibacterial activity of erythromycin. The synergistic effect may serve as remedy for bacterial infections in which the test bacteria have been implicated.

Metrics

Metrics Loading ...

References

Ereshefsky L, Dugan D. Review of the pharmacokinetics, pharmacogenetics, and drug interaction potential of antidepressants: focus on venlafaxine. Depression and Anxiety, 2000; 12(Supp. 1): 30-44.

Ereshefsky L, Jhee S, Grothe D. Antidepresant drug-drug interaction profile update. Drugs in R&D. 2005; 6(6): 323-336.

Becker ML, Kallewaard M, Caspers PW, Schalekamp T, Stricker BH. Potential determinants of drug-drug interaction associated dispensing in community pharmacies. Drug Safety. 2005; 28(5): 371-378.

Ereshefsky L. Antidepressant pharmacodynamics, pharmacokinetics and drug interactions. Geriatrics. 1998; 53(suppl. 4): S22-S33.

Hall MJ, Duncan IB. Antiviral drug and interferon combinations. In: H.J Fields (ed), Antiviral Agents: The Development and Assessment of Antiviral Chemotherapy. 1988; II:29-84. CRC Press, Boca Raton, FL.

Einarson TR, Metge CJ, Iskedjian M, Mukherjee J. An examination of the effect of cytochrome P450 drug interactions of hydroxymethylglutaryl-coenzyme A reductase inhibitors on health care utilization: a Canadian population-based study. Clinical Therapeutics. 2002; 24(12): 2126–2136.

Juurlink DN, Mamdani M, Kopp A, Laupacis A, Redelmeier DA. Drug-drug interactions among elderly patients hospitalized for drug toxicity. JAMA. 2003; 289(13): 1652–1658.

Becker ML, Kallewaard M, Caspers PW, Visser LE, Leufkens HG, Striker BH. Hospitalizations and emergency department visits due to drug-drug interactions: a literature review. Pharmacoepidemiology and Drug Safety. 2007; 16(6): 641-51.

Leone R, Magro L, Moretti U, Cutroneo P, Moschini M, Motola D, Taccori M, Conforti A. Identifying adverse drug reactions associated with drug-drug interactions: data mining of a spontaneous reporting database in Italy. Drug Safety. 2010; 33(8): 667-75.

Davies EC, Green CF, Taylor S, Williamson PR, Mottram DR, Pirmohamed M. Adverse drug reactions in hospital inpatients: a prospective analysis of 3695 patient-episodes. PLoS ONE. 2009; 4(2): e4439.

Alfaro CL. Emerging role of drug interaction studies in drug development: the good, the bad, and the unknown. Psychopharmacology Bulletin. 2001; 35(4): 80–93.

Yap YG, Camm AJ. Potential cardiac toxicity of H1-antihistamines. Clinical Allergy and Immunology. 2002; 17: 389–419.

Chen YF, Avery AJ, Neil KE, Johnson C, Dewey ME, Stockley IH. Incidence and possible causes of prescribing potentially hazardous/contraindicated drug combinations in general practice. Drug Safety. 2005; 28(1): 67-80.

Astrand B, Astrand E, Antonov K, Petersson G. Detection of potential drug interactions - a model for a national pharmacy register. European Journal of Clinical Pharmacology. 2006; 62(9): 749-56.

Shapiro LE, Shear NH. Drug-drug interactions: how scared should we be? CMAJ. 1999; 161(10): 1266-1267.

Obreli Neto PR, Nobili A, de Lyra DP. Jr., Pilger D, Guidoni CM, de Oliveira Baldoni A, Cruciol-Souza JM, de Carvalho Freitas AL, Tettamanti M, Gaeti WP, Nakamura Cuman RK. Incidence and predictors of adverse drug reactions caused by drug-drug interactions in elderly outpatients: a prospective cohort study. Journal of Pharmacy and Pharmaceutical Sciences. 2012; 15(2), 332-343.

Parsad D, Pandhi R, Dogra S. A guide to selection and appropriate use of macrolides in skin infections. American Journal of Clinical Dermatology. 2003; 4(6): 389-397.

Geo FB, Janet SB, Stephen AM, Jawetz Melnick and Adelberg’s. Medical Microbiology, Antibiotics Chemotherapy. McGraw Hill Company Inc.USA.23rd eds. 2004; 170-2.

Curry JI, Lander TD, Stringer MD. Review article: Erythromycin as a prokinetic agent in infants and children. Alimentary Pharmacology and Therapeutics. 2001; 15(5): 595-603.

Stewart JJ, Wood MJ, Parish RC, Wood CD. Prokinetic effects of erythromycin after antimotion sickness drugs. Journal of Clinical Pharmacology. 2000; 40(4): 347-353.

Pal S. A journey across the sequential development of macrolides and ketolides related to erythromycin. Tetrahedron. 2006; 62(14): 3171-3200.

Peeters T, Matthijs G, Depoortere I, Cachet T, Hoogmartens J, Vantrappen G. Erythromycin is a motilin receptor agonist. American Journal of Physiology. 1989; 257(3 Pt 1): 470-4.

Hunt CM, Watkins PB, Saenger P, Stave GM, Barlascini N, Watlington CO, Wright JT, Guzelian PS. Heterogeneity of CYP3A isoforms metabolizing erythromycin and cortisol. Clinical Pharmacology and Therapeutics. 1992; 51(1): 18-23.

Ray WA, Murray KT, Meredith S, Narasimhulu SS, Hall K, Stein CM. Oral Erythromycin and the Risk of sudden Death from Cardiac Causes. The New England Journal of Medicine. 2004; 351(11): 1089-96.

Branigan TA, Robbins RA, Cady WJ, Nickols JG, Ueda CT. The effects of erythromycin on the absorption and disposition kinetics of theophyline. European Journal of Clinical Pharmacology. 1981; 21(2): 115-120.

Zimmermann T, Yeates RA, Laufen H, Scharpf F, Leitold M, Wildfeuer A. Influence of the antibiotic erythromycin and azithromycin on the pharmacokinetics and pharmacodynamics of midazolam. Arzneimittelforschung. 1996; 46(2): 213-217.

Olajuyigbe OO, Adekola OO. In vitro interaction of erythromycin and polyvalent metallic ions (antacid) against clinical bacterial isolates. Pharmacologia. 2012; 3(7): 221-226.

Baird JK. Effectiveness of antimalarial drugs. The New England Journal of Medicine. 2005; 352(15): 1565–1577.

Clinical and Laboratory Standard Institute (CLSI): Performance Standards for Antimicrobial Susceptibility Testing; Eighteenth informational supplement; M100-S18; Pennsylvania, PA, USA. 2008; 28(1): 46–52.

Zhanel GG, Dueck M, Hoban DJ, Vercaigne LM, Embil JM, Gin AS, Karlowsky WA. Review of macrolides and ketolides focuses on respiratory tract infections. Drugs. 2001; 61(4): 443-498.

White NJ. Drug treatment and prevention of malaria. European Journal of Clinical Pharmacology. 1988; 34: 1-14.

Cheesbrough M. District laboratory practice in tropical countries, 1st edn., Cambridge University Press, Cambridge, UK. 2006; 434.

Sultana N, Arayne MS, Ghazali FA. Effect of antacids on the dissolution behaviour of methacycline and doxycycline. Journal of the Parkistan Medical Association. 1984; 34: 59.

Olajuyigbe OO, Animashaun T. Synergistic activities of amoxicillin and erythromycin against bacteria of medical importance. Pharmacologia. 2012; 3(9): 450-455.

Olajuyigbe OO, Afolayan AJ. In vitro synergy and time-kill assessment of interactions between kanamycin and metronidazole against resistant bacteria. Tropical Journal of Pharmaceutical Research. 2015; 14(5): 837-843.

Olajuyigbe OO, Adeoye-Isijola MO, Adedayo O. Synergistic potentials of benzylpenicillin, amoxicillin and streptomycin antibiotics against selected bacterial species. Life Science Journal, 2016; 13(8): 37-44. https://doi.org/10.7537/marslsj130816.07

Padgham C, Richens A. Quinine metabolism as an index of hepatic drug-metabolizing capacity. British Society of Clinical Pharmacology, 1974; 1 (4): 352-53.

Fischer VW, Fitch CD. Affinity of chloroquine for bone. Journal of Pharmacy and Pharmacology. 1975; 27(7): 527-529.

Khan B, Brandling-Bennet AD, Watkins WM, Koech DK. Plasmodium falciparum sensitivity to erythromycin and 4-aminoquinoline combination in vitro. Annals of Tropical Medicine and Parasitology. 1991; 85(2): 215-220.

Gershon PD, Howells RE. Combination of the antibiotics erythromycin and tetracycline with three standard antimalarials against Plasmodium falciparum in vitro. Annals of Tropical Medicine and Parasitology. 1984; 78(1): 1-11.

Nakornchai S, Konthiang P. Activity of azithromycin or erythromycin in combination with antimalarial drugs against multidrug-resistant Plasmodium falciparum in vitro. Acta Tropica. 2006; 100(3): 185-191.

Pinichpongse S, Doberstyn EB, Cullen JR, Yisunsri L, Thongsombun Y, Thimasarn K. An evaluation of five regimens for the out-patient therapy of falciparum malaria in Thailand 1980-81. Bulletin of the World Health Organisation. 1982; 60: 907-912.

Watt G, Loesuttivibool L, Shanks GD, Boudreau EF, Brown AE, Pavanand K, Webster HK, Wechgritaya S. Quinine with tetracycline for the treatment of drug-resistant falciparum malaria in Thailand. American Journal of Tropical Medicine and Hygiene. 1992; 47(1): 108–111.

Looareesuwan S, Vanijanonta S, Viravan C, Wilairatana P, Charoenlarp P, Lasserre R, Canfield C, Kyle DE, Webster HK. Randomised trial of mefloquine–tetracycline and quinine–tetracycline for acute uncomplicated falciparum malaria. Acta Tropica. 1994; 57(1): 47–53.

Chongsuphajaisiddhi T, Sabchareon A, Attanath P. Treatment of quinine resistant falciparum malaria in Thai children. Southeast Asian Journal of Tropical Medicine and Public Health. 1983; 14: 357–362.

Pieren M, Tigges M. Adjuvant strategies for potentiation of antibiotics to overcome antimicrobial resistance. Current Opinion in Pharmacology. 2012; 12(5): 551-555.

Clancy CJ, Nguyen MH. The combination of amphotericin B and azithromycin as a potential new therapeutic approach to fusariosis. Journal of Antimicrobial Chemotherapy. 1998; 41(1): 127-130.

Oliver BG, Silver PM, Marie C, Hoot SJ, Leyde SE, White TC. Tetracycline alters drug susceptibility in Candida albicans and other pathogenic fungi. Microbiology. 2008; 154(Pt 3): 960-970.

Garza RG, Xiong L, Zhong P, Mankin A. Binding site of macrolides antibiotics on the ribosomes; new resistance identifies a specific interaction of ketolides with rRNA. Bacteriology. 2001; 183(23): 6898-6907.

Chitum HS, Champney WS. Erythromycin inhibits the assembly of the large ribosomal subunit in growing Escherichia coli. Current Microbiology. 1995; 30(5): 273-9.

Abdelghaffar H, Soukri A, Babin- Chevaye C, Labro MT. Interaction of macrolides and ketolides with the phagocyte cell line PLB-985. Journal of Chemotherapy. 2003; 15(4): 350-356.

Floss HG, Yu TW. Rifamycin-mode of action, resistance and biosynthesis. Chemical Reviews. 2005; 105(2): 621-632.

Sultana N, Arayne MS. Drug antibiotic interactions-antimalarials. Journal of the Pakistan Medical Association. 1986; 36(2): 37-40.

Vakulenko SB, Mobashery S. Versatility of aminoglycosides and prospects for their future. Clinical Microbiology Reviews. 2003; 16(3): 430-50.

Straus SK, Hancock RE. Mode of action of the new antibiotic for Gram-positive pathogens daptomycin: comparison with cationic antimicrobial peptides and lipopeptides. Biochimica Biophysica Acta. 2006; 1758(9): 1215-1223.

Morones-Ramirez JR, Winkler J, Spina CS, Collins JJ. Silver enhances antibiotic activity against Gram-negative bacteria. Science Translational Medicine. 2013; 5(190): 190ra81.

Olajuyigbe OO, Olajuyigbe AA, Afolayan AJ. Ultrastructure and X-ray microanalysis of the antibacterial effects of stem bark ethanol extract of Acacia mearnsii De Wild against Some Selected Bacteria, Journal of Pure and Applied Microbiology. 2018; 12(4): 2217-2228.

Lin Y, Sun Z. Current views on type II diabetes. Journal of Endocrinology. 2010; 204(1): 1–11.

Downloads

Published

2021-02-28

How to Cite

Oluremi Adejoke Akinwale, Uyi Oluwatobi Emokpae, Opeyemi Mariam Adebogun, Morenike Olutumbi Adeoye-Isijola, & Olufunmiso Olusola Olajuyigbe. (2021). In vitro effects of quinine on the antibacterial activity of erythromycin against bacteria of clinical relevance. GSC Biological and Pharmaceutical Sciences, 14(2), 077–086. https://doi.org/10.30574/gscbps.2021.14.2.0033

Issue

Section

Original Article