Determination of antibacterial activity of polyenzyme preparations Gumseb using in vitro methods.

Hindustan antibiotics bulletin Pub Date : 2005-02-01
Antita Joshi, Varsha Shahane, Varsha Gore, Anju Kagal, Shilpa Risbud, Renu Bharadwaj
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Abstract

A novel polyenzyme formulation Gumseb developed by Advanced Enzyme Technologies Ltd, Thane and Speciality Biochemicals Co., USA, was tested for antibacterial properties using ATCC strains and clinical isolates of Salmonella typhi, Pseudomonas aeruginosa, Escherichia coli, Staphylococcus aureus, Streptococcus pyogenes and Streptococcus pneumoniae. A modified antibiotic susceptibility test was used for the purpose. S. aureus, S. pyogenes and S. pneumoniae were found to be sensitive to the formulation at the chosen concentration. Next, to study the interaction between Gumseb and currently used antibiotic, a checkerboard Minimum Inhibitory Concentrations (MIC) was carried out for each organism. The assay was carried out with the aim of establishing whether the polyenzyme formulation had any potentiating effect on the antibiotic of choice. Synergistic effect was established when Gumseb was used in conjunction with penicillin against S. pyogenes. Partial synergy was established when it was used in conduction with Ceftazidime against P. aeruginosa and with Ciprofloxacin against methicillin sensitive, coagulase positive S. aureus. Antagonism was established when it was used in conjunction with Ampicillin against E. coli, with Ciprofloxacin against S. typhi and coagulase negative staphylococcal strain. The results indicate that Gumseb can be used in conjunction with those antibiotics with which a synergistic or a partially synergistic effect could be shown, as in the case of P. aerugionosa and S. aureus. These findings have particular importance since these organisms are responsible for hospital based infections and are notorious for antibiotic resistance. In cases where antagonism was established, it should not be used in combination with that particular antibiotic. However, it can be used individually since it has proved to have antibacterial activity and MIC could be determined for all five commonly encountered pathogens. Therefore, it has the potential of being a novel broad range antibacterial drug. These findings are significant given the alarming rise in incidence of antibiotic resistance in most clinically important pathogens.

多酶制剂Gumseb的体外抑菌活性测定。
采用ATCC菌株和临床分离的伤寒沙门氏菌、铜绿假单胞菌、大肠杆菌、金黄色葡萄球菌、化脓性链球菌和肺炎链球菌,对美国Thane和specialty Biochemicals公司开发的新型多酶制剂Gumseb进行了抗菌性能测试。采用改良的抗生素药敏试验。金黄色葡萄球菌、化脓性葡萄球菌和肺炎葡萄球菌在选定的浓度下对该制剂敏感。接下来,为了研究Gumseb与目前使用的抗生素之间的相互作用,对每种微生物进行了棋盘最小抑制浓度(MIC)。该试验的目的是确定多酶制剂是否对所选抗生素有任何增强作用。当Gumseb与青霉素联合使用时,对化脓性葡萄球菌有协同作用。当它与头孢他啶传导抗铜绿假单胞菌和与环丙沙星传导抗甲氧西林敏感,凝固酶阳性金黄色葡萄球菌时,部分协同作用建立。当它与氨苄西林联合使用对抗大肠杆菌,与环丙沙星联合使用对抗伤寒链球菌和凝固酶阴性葡萄球菌菌株时,拮抗作用被确立。结果表明,Gumseb可与具有增效或部分增效作用的抗生素联合使用,如铜绿假单胞菌和金黄色葡萄球菌。这些发现特别重要,因为这些微生物是医院感染的原因,并且因抗生素耐药性而臭名昭著。在拮抗作用已确定的情况下,不应与该特定抗生素联合使用。然而,它可以单独使用,因为它已被证明具有抗菌活性,并且可以确定所有五种常见病原体的MIC。因此,它具有成为一种新型的广谱抗菌药物的潜力。鉴于大多数临床重要病原体抗生素耐药性发生率的惊人上升,这些发现具有重要意义。
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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