Genetic Diversity of Salp15 in the Ixodes ricinus Complex (Acari: Ixodidae)

被引:11
作者
Wang, Xin [1 ,2 ]
Huang, Yong [1 ]
Niu, Si-bo [3 ]
Jiang, Bao-Gui [1 ]
Jia, Na [1 ]
van der Geest, Leo [4 ]
Ni, Xue-bing [1 ]
Sun, Yi [1 ,2 ]
Cao, Wu-Chun [1 ]
机构
[1] Beijing Inst Microbiol & Epidemiol, State Key Lab Pathogen & Biosecur, Beijing, Peoples R China
[2] Wenzhou Ctr Dis Control & Prevent, Wenzhou, Peoples R China
[3] Chinese Acad Agr Sci, Harbin Vet Res Inst, State Key Lab Vet Biotechnol, Harbin, Peoples R China
[4] Univ Amsterdam, Inst Biodivers & Ecosyst Dynam, Sect Populat Ecol, Amsterdam, Netherlands
关键词
TICK SALIVA IMMUNOSUPPRESSOR; LYME-DISEASE SPIROCHETE; RHIPICEPHALUS-APPENDICULATUS; ANTICOAGULANT PEPTIDE; BINDING-PROTEINS; GLAND PROTEIN; SENSU-LATO; IDENTIFICATION; VECTOR; IMMUNOGLOBULIN;
D O I
10.1371/journal.pone.0094131
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Salp15, a 15-kDa tick salivary gland protein, is both essential for ticks to successfully obtain host blood and also facilitates transmission of Lyme borreliosis. To determine whether the Salp15 gene is expressed in Ixodes persulcatus and Ixodes sinensis, principle vectors of Lyme borreliosis in China, we studied transcriptions of this gene in semi-engorged larvae, nymph and adults of these two species. A total of eight Salp15 homologues, five in I. persulcatus and three in I. sinensis, were identified by reverse transcriptase-polymerase chain reaction (RT-PCR). Interestingly, the intra-species similarity of Salp15 is approximately equal to its interspecies similarity and more than one Salp15 protein is expressed in a certain tick developmental stage. Comparison of DNA and proteins with other available tick Salp15 homologues suggests that the Salp15 superfamily is genetically conserved and diverse in the Ixodes ricinus complex. These findings indicate that Salp15 proteins in the I. ricinus complex may play an essential role in interacting with the host immune system and transmission of Borrelia genospecies.
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页数:7
相关论文
共 45 条
[1]
Lyme Disease [J].
Alao, Omolara R. ;
Decker, Catherine F. .
DM DISEASE-A-MONTH, 2012, 58 (06) :335-345
[2]
Salp15, an Ixodes scapularis salivary protein, inhibits CD4+ T cell activation [J].
Anguita, J ;
Ramamoorthi, N ;
Hovius, JWR ;
Das, S ;
Thomas, V ;
Persinski, R ;
Conze, D ;
Askenase, PW ;
Rincón, M ;
Kantor, FS ;
Fikrig, E .
IMMUNITY, 2002, 16 (06) :849-859
[3]
BURGDORFER W, 1989, RHEUM DIS CLIN N AM, V15, P775
[4]
Tick saliva inhibits differentiation, maturation and function of murine bone-marrow-derived dendritic cells [J].
Cavassani, KA ;
Aliberti, JC ;
Dias, ARV ;
Silva, JS ;
Ferreira, BR .
IMMUNOLOGY, 2005, 114 (02) :235-245
[5]
Antibodies against a Tick Protein, Salp15, Protect Mice from the Lyme Disease Agent [J].
Dai, Jianfeng ;
Wang, Penghua ;
Adusumilli, Sarojini ;
Booth, Carmen J. ;
Narasimhan, Sukanya ;
Anguita, Juan ;
Fikrig, Erol .
CELL HOST & MICROBE, 2009, 6 (05) :482-492
[6]
Salp25D, an Ixodes scapularis antioxidant, is 1 of 14 immunodominant antigens in engorged tick salivary glands [J].
Das, S ;
Banerjee, G ;
DePonte, K ;
Marcantonio, N ;
Kantor, FS ;
Fikrig, E .
JOURNAL OF INFECTIOUS DISEASES, 2001, 184 (08) :1056-1064
[7]
Filippova N.A., 1991, P109
[8]
Cutting edge: CD4 is the receptor for the tick saliva immunosuppressor, Salp15 [J].
Garg, Renu ;
Juncadella, Ignacio J. ;
Ramamoorthi, Nandhini ;
Ashish ;
Ananthanarayanan, Shobana K. ;
Thomas, Venetta ;
Rincon, Mercedes ;
Krueger, Joanna K. ;
Fikrig, Erol ;
Yengo, Christopher M. ;
Anguita, Juan .
JOURNAL OF IMMUNOLOGY, 2006, 177 (10) :6579-6583
[9]
Identification of an IL-2 binding protein in the saliva of the lyme disease vector tick, Ixodes scapularis [J].
Gillespie, RD ;
Dolan, MC ;
Piesman, J ;
Titus, RG .
JOURNAL OF IMMUNOLOGY, 2001, 166 (07) :4319-4326
[10]
Characterization of the B-cell inhibitory protein factor in Ixodes ricinus tick saliva:: a potential role in enhanced Borrelia burgdoferi transmission [J].
Hannier, S ;
Liversidge, J ;
Sternberg, JM ;
Bowman, AS .
IMMUNOLOGY, 2004, 113 (03) :401-408