CLC number: S855.3
On-line Access: 2024-08-27
Received: 2023-10-17
Revision Accepted: 2024-05-08
Crosschecked: 2017-07-18
Cited: 1
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Li-bao Ma, Bao-yang Xu, Min Huang, Lv-hui Sun, Qing Yang, Yi-jie Chen, Ya-lin Yin, Qi-gai He, Hui Sun. Adjuvant effects mediated by the carbohydrate recognition domain of Agrocybe aegerita lectin interacting with avian influenza H9N2 viral surface glycosylated proteins[J]. Journal of Zhejiang University Science B, 2017, 18(8): 653-661.
@article{title="Adjuvant effects mediated by the carbohydrate recognition domain of Agrocybe aegerita lectin interacting with avian influenza H9N2 viral surface glycosylated proteins",
author="Li-bao Ma, Bao-yang Xu, Min Huang, Lv-hui Sun, Qing Yang, Yi-jie Chen, Ya-lin Yin, Qi-gai He, Hui Sun",
journal="Journal of Zhejiang University Science B",
volume="18",
number="8",
pages="653-661",
year="2017",
publisher="Zhejiang University Press & Springer",
doi="10.1631/jzus.B1600106"
}
%0 Journal Article
%T Adjuvant effects mediated by the carbohydrate recognition domain of Agrocybe aegerita lectin interacting with avian influenza H9N2 viral surface glycosylated proteins
%A Li-bao Ma
%A Bao-yang Xu
%A Min Huang
%A Lv-hui Sun
%A Qing Yang
%A Yi-jie Chen
%A Ya-lin Yin
%A Qi-gai He
%A Hui Sun
%J Journal of Zhejiang University SCIENCE B
%V 18
%N 8
%P 653-661
%@ 1673-1581
%D 2017
%I Zhejiang University Press & Springer
%DOI 10.1631/jzus.B1600106
TY - JOUR
T1 - Adjuvant effects mediated by the carbohydrate recognition domain of Agrocybe aegerita lectin interacting with avian influenza H9N2 viral surface glycosylated proteins
A1 - Li-bao Ma
A1 - Bao-yang Xu
A1 - Min Huang
A1 - Lv-hui Sun
A1 - Qing Yang
A1 - Yi-jie Chen
A1 - Ya-lin Yin
A1 - Qi-gai He
A1 - Hui Sun
J0 - Journal of Zhejiang University Science B
VL - 18
IS - 8
SP - 653
EP - 661
%@ 1673-1581
Y1 - 2017
PB - Zhejiang University Press & Springer
ER -
DOI - 10.1631/jzus.B1600106
Abstract: Objective: To evaluate the potential adjuvant effect of Agrocybe aegerita lectin (AAL), which was isolated from mushroom, against a virulent H9N2 strain in vivo and in vitro. Methods: In trial 1, 50 BALB/c male mice (8 weeks old) were divided into five groups (n=10 each group) which received a subcutaneous injection of inactivated H9N2 (control), inactivated H9N2+0.2% (w/w) alum, inactivated H9N2+0.5 mg recombinant AAL/kg body weight (BW), inactivated H9N2+1.0 mg AAL/kg BW, and inactivated H9N2+2.5 mg AAL/kg BW, respectively, four times at 7-d intervals. In trial 2, 30 BALB/c male mice (8 weeks old) were divided into three groups (n=10 each group) which received a subcutaneous injection of inactivated H9N2 (control), inactivated H9N2+2.5 mg recombinant wild-type AAL (AAL-wt)/kg BW, and inactivated H9N2+2.5 mg carbohydrate recognition domain (CRD) mutant AAL (AAL-mutR63H)/kg BW, respectively, four times at 7-d intervals. Seven days after the final immunization, serum samples were collected from each group for analysis. Hemagglutination assay, immunogold electron microscope, lectin blotting, and co-immunoprecipitation were used to study the interaction between AAL and H9N2 in vitro. Results: IgG, IgG1, and IgG2a antibody levels were significantly increased in the sera of mice co-immunized with inactivated H9N2 and AAL when compared to mice immunized with inactivated H9N2 alone. No significant increase of the IgG antibody level was detected in the sera of the mice co-immunized with inactivated H9N2 and AAL-mutR63H. Moreover, AAL-wt, but not mutant AAL-mutR63H, adhered to the surface of H9N2 virus. The interaction between AAL and the H9N2 virus was further demonstrated to be associated with the CRD of AAL binding to the surface glycosylated proteins, hemagglutinin and neuraminidase. Conclusions: Our findings indicated that AAL could be a safe and effective adjuvant capable of boosting humoral immunity against H9N2 viruses in mice through its interaction with the viral surface glycosylated proteins, hemagglutinin and neuraminidase.
[1]Aguilar, J.C., Rodríguez, E.G., 2007. Vaccine adjuvants revisited. Vaccine, 25(19):3752-3762.
[2]Choi, J.G., Lee, Y.J., Kim, Y.J., et al., 2008. An inactivated vaccine to control the current H9N2 low pathogenic avian influenza in Korea. J. Vet. Med. Sci., 9(9):67-74.
[3]Dabaghian, M., Latify, A.M., Tebianian, M., et al., 2014. Vaccination with recombinant 4×M2e.HSP70c fusion protein as a universal vaccine candidate enhances both humoral and cell-mediated immune responses and decreases viral shedding against experimental challenge of H9N2 influenza in chickens. Vet. Microbiol., 174(1-2):116-126.
[4]Dodson, J.M., Lenkowski, P.W., Eubanks, A.C., et al., 1999. Infection and immunity mediated by the carbohydrate recognition domain of the Entamoeba histolytica Gal/ GalNAc lectin. J. Infect. Dis., 179(2):460-466.
[5]Feng, L., Sun, H., Zhang, Y., et al., 2010. Structural insights into the recognition mechanism between an antitumor galectin AAL and the Thomsen-Friedenreich antigen. FASEB J., 24(10):3861-3868.
[6]Gao, W., Sun, Y., Chen, S., et al., 2013. Mushroom lectin enhanced immunogenicity of HBV DNA vaccine in C57BL/6 and HBsAg-transgenic mice. Vaccine, 31(18):2273-2280.
[7]Huang, L., Ikejiri, A., Shimizu, Y., et al., 2008. Immunoadjuvant activity of crude lectin extracted from Momordica charantia seed. J. Vet. Med. Sci., 70(5):533-535.
[8]Jung, H.J., Kim, Y.H., Song, T.J., et al., 2011. Adjuvant effect of Korean mistletoe lectin on mucosal immunity induction following intranasal immunization with hemagglutinin antigen. Food Sci. Biotechnol., 20(3):629-634.
[9]Kim, J.C., Yoon, T.J., Song, T.J., et al., 2011. Mucosal immunoadjuvant activity of Korean mistletoe lectin-C. Korean J. Food Sci. Technol., 43(1):72-76.
[10]Klenk, H.D., Wagner, R., Heuer, D., et al., 2001. Importance of hemagglutinin glycosylation for the biological functions of influenza virus. Virus Res., 82(1-2):73-75.
[11]Kong, X., Rui, R., Li, X., et al., 2004. Effects of Chinese herbal medicinal ingredients on peripheral lymphocyte proliferation and serum antibody titer after vaccination in chicken. Int. Immunopharmacol., 4(7):975-982.
[12]Kong, X.F., Hu, Y.L., Yin, Y.L., et al., 2006. Chinese herbal ingredients are effective immune stimulators for chickens infected with the Newcastle disease virus. Poultry Sci., 85(12):2169-2175.
[13]Kreisman, L.S., Cobb, B.A., 2012. Infection, inflammation and host carbohydrates: a Glyco-Evasion Hypothesis. Glycobiology, 22(8):1019-1030.
[14]Li, D., Xue, M., Wang, C., et al., 2011. Bursopentine as a novel immunoadjuvant enhances both humoral and cell-mediated immune responses to inactivated H9N2 avian influenza virus in chickens. Clin. Vacc. Immunol., 18(9):1497-1502.
[15]Lindblad, E.B., 2004. Aluminium compounds for use in vaccines. Immunol. Cell Biol., 82(5):497-505.
[16]Liu, J.H., Okazaki, K., Shi, W.M., et al., 2003. Phylogenetic analysis of hemagglutinin and neuraminidase genes of H9N2 viruses isolated from migratory ducks. Virus Genes, 27(3):291-296.
[17]Liu, M.A., 1998. Vaccine developments. Nat. Med., 4(5):515-519.
[18]Matsumura, K., Higashida, K., Ishida, H., et al., 2007. Carbohydrate binding specificity of a fucose-specific lectin from Aspergillus oryzae: a novel probe for core fucose. J. Biol. Chem., 282(21):15700-15708.
[19]Pena, L., Sutton, T., Chockalingam, A., et al., 2013. Influenza viruses with rearranged genomes as live-attenuated vaccines. J. Virol., 87(9):5118-5127.
[20]Rabinovich, G., Croci, D., 2012. Regulatory circuits mediated by lectin-glycan interactions in autoimmunity and cancer. Immunity, 36(3):322-335.
[21]Rahman, M.M., Uyangaa, E., Han, Y.W., et al., 2012. Enhancement of Th1-biased protective immunity against avian influenza H9N2 virus via oral co-administration of attenuated Salmonella enterica serovar Typhimurium expressing chicken interferon-α and interleukin-18 along with an inactivated vaccine. BMC Vet. Res., 8:105.
[22]Rajik, M., Jahanshiri, F., Omar, A.R., et al., 2009. Identification and characterisation of a novel anti-viral peptide against avian influenza virus H9N2. Virol. J., 6:74.
[23]Rajput, Z.I., Hu, S.H., Xiao, C.W., et al., 2007. Adjuvant effects of saponins on animal immune responses. J. Zhejiang Univ.-Sci. B (Biomed. & Biotechnol.), 8(3):153-161.
[24]Reitter, J.N., Means, R.E., Desrosiers, R.C., 1998. A role for carbohydrates in immune evasion in AIDS. Nat. Med., 4(6):679-684.
[25]Sivakumar, S.M., Safhi, M.M., Kannadasan, M., et al., 2011. Vaccine adjuvants—current status and prospects on controlled release adjuvancity. Saudi Pharm. J., 19(4):197-206.
[26]Sun, H., Zhao, C.G., Tong, X., et al., 2003. A lectin with mycelia differentiation and antiphytovirus activities from the edible mushroom Agrocybe aegerita. J. Biochem. Mol. Biol., 36(2):214-222.
[27]Sun, L.H., Li, J.G., Zhao, H., et al., 2013. Porcine serum can be biofortified with selenium to inhibit proliferation of three types of human cancer cells. J. Nutr., 143(7):1115-1122.
[28]Sun, L.H., Lei, M.Y., Zhang, N.Y., et al., 2014. Hepatotoxic effects of mycotoxin combinations in mice. Food Chem. Toxicol., 74:289-293.
[29]Sun, Y., Liu, J., 2008. Adjuvant effect of water-soluble polysaccharide (PAP) from the mycelium of Polyporus albicans on the immune responses to ovalbumin in mice. Vaccine, 26(31):3932-3936.
[30]Tsuchiya, E., Sugawara, K., Hongo, S., et al., 2002a. Effect of addition of new oligosaccharide chains to the globular head of influenza A/H2N2 virus haemagglutinin on the intracellular transport and biological activities of the molecule. J. Gen. Virol., 83(5):1137-1146.
[31]Tsuchiya, E., Sugawara, K., Hongo, S., et al., 2002b. Role of overlapping glycosylation sequons in antigenic properties, intracellular transport and biological activities of influenza A/H2N2 virus haemagglutinin. J. Gen. Virol., 83(12):3067-3074.
[32]Ung, C.Y., Li, H., Kong, C.Y., et al., 2007. Usefulness of traditionally defined herbal properties for distinguishing prescriptions of traditional Chinese medicine from non-prescription recipes. J. Ethnopharmacol., 109(1):21-28.
[33]Yamaguchi, N., Sonoyama, K., Kikuchi, H., et al., 2005. Gastric colonization of Candida albicans differs in mice fed commercial and purified diets. J. Nutr., 135(1):109-115.
[34]Yang, L., Hu, Y., Xue, J., et al., 2008. Compound Chinese herbal medicinal ingredients can enhance immune response and efficacy of RHD vaccine in rabbit. Vaccine, 26(35):4451-4455.
[35]Yang, N., Tong, X., Xiang, Y., et al., 2005. Molecular character of the recombinant antitumor lectin from the edible mushroom Agrocybe aegerita. J. Biochem., 138(2):145-150.
[36]Liang, Y., Lei, F., Xin, T., et al., 2009. Importance of nuclear localization for the apoptosis-induced activity of a fungal galectin AAL (Agrocybe aegerita lectin). Biochem. Biophys. Res. Commun., 386(3):437-442.
[37]Zhao, C., Sun, H., Tong, X., et al., 2003. An antitumour lectin from the edible mushroom Agrocybe aegerita. Biochem. J., 374(2):321-327.
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