Variation in the salivary peptide, maxadilan, from species in the Lutzomyia longipalpis complex

被引:70
作者
Lanzaro, GC
Lopes, AHCS
Ribeiro, JMC
Shoemaker, CB
Warburg, A
Soares, M
Titus, RG
机构
[1] Univ Texas, Med Branch, Dept Pathol, Galveston, TX 77555 USA
[2] Univ Texas, Med Branch, Ctr Trop Dis, Galveston, TX 77555 USA
[3] Fed Univ Rio De Janeiro, Inst Microbiol, BR-21941590 Rio De Janeiro, Brazil
[4] NIAID, Parasit Dis Lab, NIH, Bethesda, MD 20892 USA
[5] Harvard Univ, Sch Publ Hlth, Dept Trop Publ Hlth, Boston, MA 02115 USA
[6] Hebrew Univ Jerusalem, Hadassah Med Sch, Dept Parasitol, IL-91120 Jerusalem, Israel
[7] Fdn Oswaldo Cruz, Ctr Pesquisas Goncalo Moniz, Lab Patol & Biol Celular, Salvador, BA, Brazil
[8] Colorado State Univ, Coll Vet Med & Biomed Sci, Dept Pathol, Ft Collins, CO 80523 USA
关键词
maxadilan; population genetics; saliva; vasodilator;
D O I
10.1046/j.1365-2583.1999.820267.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Maxadilan is an approximately 7 kDa peptide that occurs in the saliva of the sand fly Lutzomyia longipalpis. This peptide is a potent vasodilator and may also have immunomodulatory effects related to the pathogenesis of leishmanial infections. Variation in the primary DNA and inferred amino acid sequence of maxadilan is reported. Differences were found within and among natural field populations as well as among sibling species. Extensive amino acid sequence differentiation, up to 23%, was observed among maxadilan from different populations. This is a remarkable degree of polymorphism considering the small size of this peptide. The vasodilatory activity of maxadilan was equivalent among recombinant maxadilan variants. All maxadilan variants induce interleukin-6. Predicted secondary structure and hydrophobicity plots suggest that these characteristics are conserved among variant peptides. However, profiles based on the antigenic index do differ among peptides.
引用
收藏
页码:267 / 275
页数:9
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