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腮腺唾液富组蛋白抗菌活性的研究 被引量:4

Antibacterial activity of histidinerich polypeptides in human parotid saliva
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摘要 为探讨富组蛋白(histidinerichpolypeptides,HRPs)的抗菌作用,进一步阐明唾液的正常生理功能,我们采用二种微量且敏感的琼脂糖弥散抗菌实验,分析了腮腺唾液中HRPs的抗菌活性。研究结果不但证实HRPs对变形链球菌MT6R株确有抗菌活性,还首次发现HRPs对金黄色葡萄球菌ATCC25923株、大肠杆菌ML35P株及绿脓杆菌ATCC27853株也有很强的抗菌活性。观察表明,在腮腺唾液中起抗菌作用的主要是HRP3、HRP5和HRP6。HRPs对血链球菌S34Sr株无抗菌活性。该项研究结果表明,HRPs实际上为一组内源性广谱抗生素肽,对霉菌、革兰氏阳性与阴性细菌均有抗菌作用。HRPs除具有防龋功能外,还可能是口腔中对抗多种微生物感染的重要分子,应该进行深入研究。 Two ultrasensitive antibacterial assays were applied to determine the antibacterial activity of histidinerich polypeptides (HRPs) in human parotid saliva. The results not only confirmed the potent antibacterial activity of HRPs against Streptococcus mutans MT6R, but also showed for the first time that HRPs were effectivelly antibacterial to Staphylcococcus aureus ATCC 25923, Escherichia coli ML35p and Pseudomonas aeruginosa ATCC 27853. Among HRPs、HRP3、HRP5 and HRP6 were the major antibacterial components which were active against S. mutans,S. aureus, E. coli and P. aeruginosa, whereas HRP1 was only effective against E. coli. S. sanguis was resistant to the action of HRPs. These results suggest that HRPs are actually a family of endogenous antibiotic peptides with broad antimicrobial spectrum including fungi, Grampositive and Gramnegative bacteria and may play an important role in the prevention of various infection diseases in the oral cavity as well as in the resistance to caries.
出处 《中华口腔医学杂志》 CAS CSCD 北大核心 1997年第6期356-359,共4页 Chinese Journal of Stomatology
关键词 唾液 腮腺 内源性抗生素肽 蛋白电泳 富组蛋白 Salivarius, parotid Peptide, antibiotic, endogenic Proteinogram
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  • 1吴祖林,王立庄,蔡乾英,周安,苏姣华.苗药阿雄粉的临床初步观察及抑菌研究[J].中医杂志,1996,37(11):680-681. 被引量:4
  • 2许静,李昂,苟建重,许援朝,饶国洲,刘蒸,谢红帼.牙龈卟啉单胞菌精氨酸牙龈素催化结构域基因的克隆及其在大肠杆菌中的表达[J].华西口腔医学杂志,2006,24(5):400-403. 被引量:9
  • 3MACKAY B J, DENEPITIYA L, IACONO V J, et al. Growth-inhibitory and bactericidal effects of human parotid salivary histidine-rich polypeptides on Streptococcus mutans [ J ]. Infect Immun, 1984,44 ( 3 ) :695 - 701.
  • 4POLLOCK J J, DENEPITIYA L, MACKAY B J, et al. Fungistatic and fungicidal activity of human parotid salivary histidine-rich polypeptides on Candida albicans [ J ]. Infect Immun, 1984,44 ( 3 ) :702 - 707.
  • 5FITZGERALD D H, COLEMAN D C, O'CONNELL B C. Susceptibility of Candida dubliniensis to salivary histatin 3 [ J]. Antimicrob Agents Chemother,2003,47( 1 ) :70 -76.
  • 6RUISSEN A L, GROENINK J, LOMMERSE C H, et al. Effects of carbohydrate polymers applicable in saliva substitutes on the anti-Candida activity of a histatinderived peptide [ J ]. Arch Oral Biol, 2002,47 ( 11 ) : 749 - 756.
  • 7LEHRER R I, GANZ T. Antimicrobial peptides in mammalian and insect host defence [ J ]. Curr Opin Immunol,1999,11 ( 1 ) :23 -27.
  • 8VAN'T HOF W,VEERMAN E C,HELMERHORST E J,et al. Antimicrobial peptides: properties and applicability [J]. Biol Chem,2001,382(4) :597 -619.
  • 9LAMKIN M S, OPPENHEIM F G. Structural features of salivary function [J]. Crit Rev Oral Med ,1993 , 4 ( 3 ) :251 - 259.
  • 10KOSHLUKOVA S E, LLOYD T L, ARAUJO M W, et al. Salivary histatin 5 induces non-lytic release of ATP from Candida albicans leading to cell death [J]. J Biol Chem, 1999,274 ( 27 ) : 18872 - 18879.

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