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In vitro activity of the antimicrobial peptides human and rabbit defensins and porcine leukocyte protegrin against Mycobacterium tuberculosis.

机译:抗菌肽人和兔防御素和猪白细胞protegrin对结核分枝杆菌的体外活性。

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Three independent assay methods were used to investigate the activities of antimicrobial peptides (human and rabbit defensins and protegrin from porcine leukocytes) against Mycobacterium tuberculosis in vitro. M. tuberculosis H37Ra was cultured in the presence of human neutrophil peptide 1, synthetic rabbit neutrophil peptide 1, or porcine protegrin 1 at 37 degrees C for 6 to 48 h, and antimycobacterial activity was measured by CFU assay. These peptides at a concentration of 50 microg/ml showed significant antibacterial effects on M. tuberculosis after 24 and 48 h of incubation (85.9 to 97.5% at 24 h and 91.6 to 99.4% at 48 h). A radiometric method and a radial diffusion assay confirmed these observations. Antibacterial activity against M. tuberculosis was independent of calcium (1.0 mM) or magnesium (1.0 mM) and not inhibited by sodium chloride (100 mM). The optimal pH for antibacterial activity against M. tuberculosis was greater than 4.0. Three clinical isolates of M. tuberculosis were also studied, and these peptides showed 86.3 to 99.0% reduction in CFU of these organisms. Morphological studies using scanning electron microscopy showed that defensins caused lesions on the surface of H37Ra. These observations suggest that antimicrobial peptides such as defensins and protegrins may represent an important component of the host defense mechanism against M. tuberculosis and offer a potential new approach to therapy.
机译:三种独立的测定方法用于研究体外抗菌肽(猪白细胞的人和兔防御素和protegrin)对结核分枝杆菌的活性。在人嗜中性粒细胞肽1,合成兔嗜中性粒细胞肽1或猪protegrin 1的存在下,于37°C下培养结核分枝杆菌H37Ra 6至48 h,并通过CFU分析测定抗分枝杆菌活性。孵育24和48小时后,这些浓度为50微克/毫升的肽对结核分枝杆菌显示出显着的抗菌作用(24小时为85.9至97.5%,48小时为91.6至99.4%)。辐射法和径向扩散测定法证实了这些观察结果。对结核分枝杆菌的抗菌活性独立于钙(1.0 mM)或镁(1.0 mM),不受氯化钠(100 mM)的抑制。对结核分枝杆菌的抗菌活性的最佳pH值大于4.0。还研究了三种临床分离的结核分枝杆菌,这些肽显示这些微生物的CFU降低了86.3%至99.0%。使用扫描电子显微镜的形态学研究表明防御素引起H37Ra表面的损伤。这些观察结果表明,抗菌素肽(如防御素和蛋白凝集素)可能代表抗结核分枝杆菌的宿主防御机制的重要组成部分,并提供了潜在的新治疗方法。

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