Activation of an immune response in Litopenaeus vannamei by oral immunization with phagocytosis activating protein (PAP) DNA

被引:12
作者
Khimmakthong, Umaporn [1 ,2 ]
Kongmee, Pataraporn [1 ,2 ]
Deachamag, Panchalika [1 ,2 ]
Leggat, Ureporn [3 ]
Chotigeat, Wilaiwan [1 ,2 ]
机构
[1] Prince Songkla Univ, Fac Sci, Ctr Genom & Bioinformat Res, Hat Yai 90112, Songkhla, Thailand
[2] Prince Songkla Univ, Fac Sci, Dept Mol Biotechnol & Bioinformat, Hat Yai 90112, Songkhla, Thailand
[3] Prince Songkla Univ, Fac Dent, Dept Oral Biol, Hat Yai 90112, Songkhla, Thailand
关键词
DNA; Nanoparticles; Phagocytosis activating protein; Shrimp; WSSV; SPOT-SYNDROME-VIRUS; PENAEUS-MONODON; GENE DELIVERY; IN-VITRO; CHITOSAN NANOPARTICLES; PROCAMBARUS-CLARKII; MOLECULAR-MASS; SHRIMP; PROTECTION; VACCINE;
D O I
10.1016/j.fsi.2013.01.004
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
The phagocytosis activating protein (PAP) gene has been reported to stimulate the phagocytic activity of shrimp hemocytes and to protect shrimp from several pathogens. In this study oral administration of the chitosan-PAP gene to shrimp was investigated for its ability to induce immunity. The PAP gene was cooperated into a phMGFP plasmid, named PAP-phMGFP. Chitosan-PAP-phMGFP nanoparticles were formed by mixing a low molecular weight chitosan (50 kDa) and a high molecular weight chitosan (150 kDa) with various ratios of PAP-phMGFP. The optimal ratio of chitosan PAP-phMGFP nanoparticles was first determined by transfection into Chinese Hamster Ovary (CHO) cells before being used for oral immunization in shrimp. The chitosan-PAP-phMGFP nanoparticles at a ratio of 2:1 with the low molecular weight chitosan were optimum for transfecting the CHO cells. The shrimp were then fed with 25, 50,100 and 150 mu g/shrimp/day of chitosan-PAP-phMGFP (2:1) nanoparticles then challenged by the white spot syndrome virus (WSSV). Shrimp fed with 50 mu g of chitosan-PAP-phMGFP nanoparticles per day for 7 consecutive days, produced the highest relative percent survival (RPS) (94.45 +/- 9.86%). The presence of PAP-phMGFP was detected in every shrimp tissue including the hemolymph, lymphoid organ, heart, hepatopancreas, intestine and muscle. The folds increase of the PAP gene expression increased significantly together with an increase of the phagocytic activity in the immunized shrimp. The stability of the PAP-phMGFP in the immunized shrimp hemolymph was detected by determination of the expression of the GFP at various days after immunization ceased. GFP expression was detected until the 15th day but not at the 30th day after immunization ceased. A quantitative analysis of the WSSV copies in shrimp heart tissue was significantly reduced in the immunized shrimp. In addition, chitosan-PAP-phMGFP nanoparticles protected shrimp against WSSV, Yellow head virus (YHV) and Vibrio harveyi with RPS values of 83.34 +/- 7.86%, 55.56 +/- 15.72% and 53.91 +/- 5.52%, respectively. This study therefore confirms the role of the PAP gene in shrimp immunity and may lead to the development of a way to prevent microbial diseases of shrimp at an industrial level by appropriate feeding of a chitosan/DNA complex. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:929 / 938
页数:10
相关论文
共 69 条
[1]  
Alcivar-Warren A, 2007, J SHELLFISH RES, V26, P1259, DOI 10.2983/0730-8000(2007)26[1259:SALMLM]2.0.CO
[2]  
2
[3]   Chitosan as a nasal delivery system: The effect of chitosan solutions on in vitro and in vivo mucociliary transport rates in human turbinates and volunteers [J].
Aspden, TJ ;
Mason, JDT ;
Jones, NS ;
Lowe, J ;
Skaugrud, O ;
Illum, L .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1997, 86 (04) :509-513
[4]   Enhanced survival of shrimp, Penaeus (Marsupenaeus) japonicus from white spot syndrome disease after oral administration of recombinant VP28 expressed in Brevibacillus brevis [J].
Caipang, Christopher Marlowe A. ;
Verjan, Noel ;
Ooi, Ei Lin ;
Kondo, Hidehiro ;
Hirono, Ikuo ;
Aoki, Takashi ;
Kiyono, Hiroshi ;
Yuki, Yoshikazu .
FISH & SHELLFISH IMMUNOLOGY, 2008, 25 (03) :315-320
[5]   Evaluation of the biological properties of soluble chitosan and chitosan microspheres [J].
CarrenoGomez, B ;
Duncan, R .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1997, 148 (02) :231-240
[6]   CHITOSAN - AS A BIOMATERIAL [J].
CHANDY, T ;
SHARMA, CP .
BIOMATERIALS ARTIFICIAL CELLS AND ARTIFICIAL ORGANS, 1990, 18 (01) :1-24
[7]   Dietary β-1,3-glucan effectively improves immunity and survival of Penaeus monodon challenged with white spot syndrome virus [J].
Chang, CF ;
Su, MS ;
Chen, HY ;
Liao, IC .
FISH & SHELLFISH IMMUNOLOGY, 2003, 15 (04) :297-310
[8]   Identification of white spot syndrome associated baculovirus (WSBV) target organs in the shrimp Penaeus monodon by in situ hybridization [J].
Chang, PS ;
Lo, CF ;
Wang, YC ;
Kou, GH .
DISEASES OF AQUATIC ORGANISMS, 1996, 27 (02) :131-139
[9]   Gene silencing of a prophenoloxidase activating enzyme in the shrimp, Penaeus monodon, increases susceptibility to Vibrio harveyi infection [J].
Charoensapsri, Walaiporn ;
Amparyup, Piti ;
Hirono, Ikuo ;
Aoki, Takashi ;
Tassanakajon, Anchalee .
DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY, 2009, 33 (07) :811-820
[10]   Effect of fucoidan on disease resistance of black tiger shrimp [J].
Chotigeat, W ;
Tongsupa, S ;
Supamataya, K ;
Phongdara, A .
AQUACULTURE, 2004, 233 (1-4) :23-30