Sang Yongming, Ortega M Teresa, Blecha Frank, Prakash Om, Melgarejo Tonatiuh
Department of Human Nutrition, 143B Justin Hall, Kansas State University, Manhattan, KS 66506-1407, USA.
Infect Immun. 2005 May;73(5):2611-20. doi: 10.1128/IAI.73.5.2611-2620.2005.
Mammalian beta-defensins are small cationic peptides possessing broad antimicrobial and physiological activities. Because dogs are particularly resilient to sexually transmitted diseases, it has been proposed that their antimicrobial peptide repertoire might provide insight into novel antimicrobial therapeutics and treatment regimens. To investigate this proposal, we cloned the full-length cDNA of three canine beta-defensin isoforms (cBD-1, -2, and -3) from canine testicular tissues. Their predicted peptides share identical N-terminal 65-amino-acid residues, including the beta-defensin consensus six-cysteine motif. The two longer isoforms, cBD-2 and -3, possess 4 and 34 additional amino acids, respectively, at the C terminus. To evaluate the antimicrobial activity of cBD, a 34-amino-acid peptide derived from the shared mature peptide region was synthesized. Canine beta-defensin displayed broad antimicrobial activity against gram-positive bacteria (Listeria monocytogenes and Staphylococcus aureus; MICs of 6 and 100 mug/ml, respectively), gram-negative bacteria (Escherichia coli, Klebsiella pneumoniae, and Neisseria gonorrhoeae; MICs of 20 to 50, 20, and 50 mug/ml, respectively), and yeast (Candida albicans; MIC of 5 to 50 mug/ml) and lower activity against Ureaplasma urealyticum and U. canigenitalium (MIC of 200 mug/ml). Antimicrobial potency was significantly reduced at salt concentrations higher than 140 mM. All three canine beta-defensins were highly expressed in testis. In situ hybridization indicated that cBD-1 was expressed primarily in Sertoli cells within the seminiferous tubules. In contrast, cBD-2 was located primarily within Leydig cells. The longest isoform, cBD-3, was detected in Sertoli cells and to a lesser extent in the interstitium. The tissue-specific expression and broad antimicrobial activity suggest that canine beta-defensins play an important role in host defense and other physiological functions of the male reproductive system.
哺乳动物β-防御素是一类具有广泛抗菌和生理活性的小阳离子肽。由于犬类对性传播疾病具有特别的抵抗力,有人提出其抗菌肽库可能为新型抗菌疗法和治疗方案提供线索。为了研究这一设想,我们从犬类睾丸组织中克隆了三种犬β-防御素异构体(cBD-1、-2和-3)的全长cDNA。它们预测的肽段具有相同的N端65个氨基酸残基,包括β-防御素共有的六个半胱氨酸基序。两种较长的异构体cBD-2和-3在C端分别额外具有4个和34个氨基酸。为了评估cBD的抗菌活性,合成了一种源自共享成熟肽区域的34个氨基酸的肽。犬β-防御素对革兰氏阳性菌(单核细胞增生李斯特菌和金黄色葡萄球菌;最低抑菌浓度分别为6和100μg/ml)、革兰氏阴性菌(大肠杆菌、肺炎克雷伯菌和淋病奈瑟菌;最低抑菌浓度分别为20至50、20和50μg/ml)和酵母(白色念珠菌;最低抑菌浓度为5至50μg/ml)表现出广泛的抗菌活性,而对解脲脲原体和犬生殖道脲原体的活性较低(最低抑菌浓度为200μg/ml)。在盐浓度高于140 mM时,抗菌效力显著降低。所有三种犬β-防御素在睾丸中均高度表达。原位杂交表明,cBD-1主要在生精小管内的支持细胞中表达。相比之下,cBD-2主要位于睾丸间质细胞中。最长的异构体cBD-3在支持细胞中被检测到,在间质中的表达程度较低。组织特异性表达和广泛的抗菌活性表明,犬β-防御素在雄性生殖系统的宿主防御和其他生理功能中发挥着重要作用。