In Vitro Synergistic Activity of Combinations of Tetrahydroisoquinolines and Treatment Antibiotics against Multidrug-Resistant Salmonella.

IF 2.1 Q3 PHARMACOLOGY & PHARMACY
Advances in Pharmacological and Pharmaceutical Sciences Pub Date : 2023-12-13 eCollection Date: 2023-01-01 DOI:10.1155/2023/6142810
Rita Ayuk Ndip, Joelle Ngo Hanna, James Ajeck Mbah, Stephen Mbigha Ghogomu, Moses Njutain Ngemenya
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Abstract

The global burden of Salmonella infections remains high due to the emergence of multidrug resistance to all recommended treatment antibiotics. Tetrahydroisoquinolines (THIQs) have demonstrated promising activity against multidrug-resistant (MDR) Salmonella Typhi. Hence, their interaction with treatment antibiotics was investigated for possible synergy. Twenty combinations of five THIQs (1, 2, 3, 4, and 5) and four antibiotics were tested against each of 7 Salmonella isolates by the checkerboard method giving a total of 140 assays performed. Fractional inhibitory concentration indices (FICIs) were calculated, and isobolograms were plotted. In terms of FICI, synergism ranged from 0.078 to 0.5 and the highest magnitude (0.078) was recorded for chloramphenicol-THIQ 1 combination. In a total of 140 antibiotics-THIQs combination assays, 27 were synergistic (17%), 42 were additive (30%), 11 were antagonistic (7.8%), and 60 were indifferent (42%). The synergistic activity recorded for each antibiotic class in combination based on the total of 7 bacterial isolates tested ranged from 14.29% to 71.43%; the highest percentage was recorded for two combinations (chloramphenicol or sulphamethoxazole with THIQ 1). Ciprofloxacin-THIQ 1 combination showed additivity on all bacteria isolates tested (100%). Overall, THIQ 1 was the most synergistic and most additive in combination with three antibiotics (ampicillin, chloramphenicol, or sulphamethoxazole-trimethoprim). Some combinations of the THIQs and treatment antibiotics have shown high synergism which could potentially be efficacious against multidrug-resistant S. Typhi, hence this interaction should be further studied in vivo.

四氢异喹啉类和治疗抗生素组合对耐多药沙门氏菌的体外协同作用
由于出现了对所有推荐治疗抗生素的多重耐药性,全球沙门氏菌感染的负担仍然很重。四氢异喹啉类(THIQs)对耐多药(MDR)伤寒沙门氏菌具有良好的活性。因此,我们研究了它们与治疗用抗生素之间的相互作用,以寻求可能的协同作用。通过棋盘格法,对 7 种沙门氏菌分离物中的每一种进行了 5 种 THIQ(1、2、3、4 和 5)和 4 种抗生素的 20 种组合试验,共进行了 140 次试验。计算了分抑制浓度指数(FICI),并绘制了等全息图。就 FICI 而言,协同作用在 0.078 至 0.5 之间,氯霉素-THIQ 1 组合的协同作用最高(0.078)。在总共 140 项抗生素-THIQs 组合试验中,27 项具有协同作用(17%),42 项具有相加作用(30%),11 项具有拮抗作用(7.8%),60 项不具有协同作用(42%)。根据总共 7 种细菌分离物的测试结果,每类抗生素的组合协同活性从 14.29% 到 71.43% 不等;其中两种组合(氯霉素或磺胺甲噁唑与 THIQ 1)的协同活性最高。环丙沙星-THIQ 1 复方制剂对所有受试细菌分离物均有加成作用(100%)。总体而言,THIQ 1 与三种抗生素(氨苄西林、氯霉素或磺胺甲噁唑-三甲氧苄)的组合协同作用最强,相加效果最好。一些 THIQs 与治疗抗生素的组合显示出很高的协同作用,有可能对耐多药伤寒杆菌有效,因此应在体内进一步研究这种相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.30
自引率
3.60%
发文量
0
审稿时长
17 weeks
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