Drug repurposing in the context of common bacterial pathogens

Q3 Agricultural and Biological Sciences Acta Biologica Szegediensis Pub Date : 2023-05-27 DOI:10.14232/abs.2022.2.140-149
M. Donadu, S. Zanetti, B. Battah, H. Hetta, Danica Matusovits, K. Kárpáti, Virág Finta, Berta Csontos, Anna Kuklis, Fruzsina Szikora, Adrienn Csegény, Lea Szalma, Eszter Major, I. Kushkevych, M. Gajdács
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Abstract

The clinical problem of multidrug resistance (MDR) in bacteria is due to the lack of novel antibiotics in development and the dwindling pipeline of drugs receiving market authorization. Repurposing of non-antibiotic pharmacological agents may be an attractive pathway to provide new antimicrobial drugs. The aim of the present study was to ascertain the antibacterial and adjuvant properties of a wide range of pharmaceuticals against antibiotic-susceptible and drug-resistant bacteria. Sixty-five (n = 65) pharmacological agents were included in our experiments. For Gram-positive bacteria, Staphylococcus aureus ATCC 43300 (methicillin-resistant), S. epidermidis ATCC 12228, Streptococcus pyogenes ATCC 12384 and Enterococcus faecalis ATCC 29212 were used, while for Gram-negative bacteria, Enterobacter cloacae ATCC 13047 (extended-spectrum β-lactamase-positive), Klebsiella pneumoniae ATCC 49619, Serratia marcescens ATCC 29632 and Pseudomonas aeruginosa ATCC 27853 were included as representative strains. The minimum inhibitory concentrations (MICs) of the tested compounds were determined using the standard broth microdilution method, while a MIC reduction assay was included to ascertain the effect of the tested compounds on the MICs of standard antibiotics (ceftriaxone, ciprofloxacin and gentamicin). Seventeen and twelve drug molecules tested showed measurable antibacterial activities (MIC: 32-512 µg/mL) against Gram-positive and Gram-negative bacteria, respectively. Several compounds decreased the MICs of ciprofloxacin and gentamicin. Although there are increasing number of studies in this field, there are still significant gaps in the evidence to the potential use of non-antibiotic drugs in antimicrobial drug repurposing.
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在常见细菌病原体的背景下药物再利用
细菌多药耐药(MDR)的临床问题是由于缺乏正在开发的新型抗生素和获得市场授权的药物管道减少。非抗生素药物的再利用可能是提供新型抗菌药物的一个有吸引力的途径。本研究的目的是确定各种药物对抗生素敏感和耐药细菌的抗菌和辅助特性。我们的实验包括65种(n = 65)药物。革兰氏阳性菌以金黄色葡萄球菌ATCC 43300(耐甲氧西林)、表皮葡萄球菌ATCC 12228、化脓性链球菌ATCC 12384和粪肠球菌ATCC 29212为代表菌株,革兰氏阴性菌以阴沟肠杆菌ATCC 13047(广谱β-内酰胺酶阳性)、肺炎克雷伯菌ATCC 49619、粘质沙雷菌ATCC 29632和铜绿假单胞菌ATCC 27853为代表菌株。采用标准肉汤微量稀释法测定被试化合物的最低抑菌浓度(MIC),并采用MIC还原法测定被试化合物对标准抗生素(头孢曲松、环丙沙星和庆大霉素)MIC的影响。对革兰氏阳性菌和革兰氏阴性菌的抑菌活性分别为17个和12个,MIC值为32 ~ 512µg/mL。一些化合物降低环丙沙星和庆大霉素的mic。尽管这一领域的研究越来越多,但在抗菌药物再利用中非抗生素药物的潜在使用证据方面仍存在重大差距。
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来源期刊
Acta Biologica Szegediensis
Acta Biologica Szegediensis Agricultural and Biological Sciences-Agricultural and Biological Sciences (all)
CiteScore
1.00
自引率
0.00%
发文量
14
期刊介绍: Acta Biologica Szegediensis (ISSN 1588-385X print form; ISSN 1588-4082 online form), a member of the Acta Universitatis Szegediensis family of scientific journals (ISSN 0563-0592), is published yearly by the University of Szeged. Acta Biologica Szegediensis covers the growth areas of modern biology and publishes original research articles and reviews, involving, but not restricted to, the fields of anatomy, embryology and histology, anthropology, biochemistry, biophysics, biotechnology, botany and plant physiology, all areas of clinical sciences, conservation biology, ecology, genetics, microbiology, molecular biology, neurosciences, paleontology, pharmacology, physiology and pathophysiology, and zoology.
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