Bacterial membranes enhance the immunogenicity and protective capacity of the surface exposed tick Subolesin-Anaplasma marginale MSP1a chimeric antigen

被引:8
作者
Contreras, Marinela [1 ]
Moreno-Cid, Juan A. [1 ]
Domingos, Ana [2 ]
Canales, Mario [1 ]
Diez-Delgado, Iratxe [1 ]
Perez de la Lastra, Jose M. [1 ]
Sanchez, Emilio [1 ]
Merino, Octavio [3 ]
Lopez Zavala, Rigoberto [3 ]
Ayllon, Nieves [1 ]
Boadella, Mariana [1 ]
Villar, Margarita [1 ]
Gortazar, Christian [1 ]
de la Fuente, Jose [1 ,4 ]
机构
[1] Inst Invest Recursos Cineget IREC CSIC UCLM JCCM, SaBio, Ciudad Real 13005, Spain
[2] Ctr Malaria & Outras Doencas Trop, Inst Higiene & Med Trop, P-1349008 Lisbon, Portugal
[3] Univ Autonoma Tamaulipas, Fac Med Vet & Zootecnia, Ciudad Victoria 87000, Tamaulipas, Mexico
[4] Oklahoma State Univ, Dept Vet Pathobiol, Ctr Vet Hlth Sci, Stillwater, OK 74078 USA
关键词
Chimera; Endotoxin; Immunology; MSP1a; Subolesin; Tick; Vaccine; VECTOR INFESTATIONS; VACCINE; PROTEIN; PEPTIDES;
D O I
10.1016/j.ttbdis.2015.07.010
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Ticks are vectors of diseases that affect humans and animals worldwide. Tick vaccines have been proposed as a cost-effective and environmentally sound alternative for tick control. Recently, the Rhipicephalus microplus Subolesin (SUB)-Anaplasma marginale MSP1a chimeric antigen was produced in Escherichia coli as membrane-bound and exposed protein and used to protect vaccinated cattle against tick infestations. In this research, lipidomics and proteomics characterization of the E. coli membrane-bound SUB-MSP1a antigen showed the presence of components with potential adjuvant effect. Furthermore, vaccination with membrane-free SUB-MSP1a and bacterial membranes containing SUB-MSP1a showed that bacterial membranes enhance the immunogenicity of the SUB-MSP1a antigen in animal models. R. microplus female ticks were capillary-fed with sera from pigs orally immunized with membrane-free SUB, membrane bound SUB-MSP1a and saline control. Ticks ingested antibodies added to the blood meal and the effect of these antibodies on reduction of tick weight was shown for membrane bound SUB-MSP1a but not SUB when compared to control. Using the simple and cost-effective process developed for the purification of membrane-bound SUB-MSP1a, endotoxin levels were within limits accepted for recombinant vaccines. These results provide further support for the development of tick vaccines using E. coli membranes exposing chimeric antigens such as SUB-MSP1a. (C) 2015 Elsevier GmbH. All rights reserved.
引用
收藏
页码:820 / 828
页数:9
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