您好,欢迎访问中国水产科学研究院 机构知识库!

Expression profiles of the p38 MAPK signaling pathway from Chinese shrimp I Fenneropenaeus chinensis in response to viral and bacterial infections

文献类型: 外文期刊

作者: He, Yuying 1 ; Yao, Wanlong 3 ; Liu, Ping 1 ; Li, Jian 1 ; Wang, Qingyin 1 ;

作者机构: 1.Chinese Acad Fishery Sci, Yellow Sea Fisheries Res Inst, Minist Agr, Key Lab Sustainable Dev Marine Fisheries, Qingdao 266071, Peoples R China

2.Qingdao Natl Lab Marine Sci & Technol, Funct Lab Marine Fisheries Sci & Food Prod Proc, Qingdao 266200, Peoples R China

3.Shanghai Ocean Univ, Coll Fisheries & Life Sci, Shanghai 201306, Peoples R China

关键词: Fenneropenaeus chinensis;Expression profiles;p38;WSSV;Bacteria;RNA interference (RNAi)

期刊名称:GENE ( 影响因子:3.688; 五年影响因子:3.329 )

ISSN: 0378-1119

年卷期: 2018 年 642 卷

页码:

收录情况: SCI

摘要: Mitogen-activated protein kinase (MAPK) signaling pathway plays an important role in cellular response to inflammatory cytokines, environmental stress and pathogenic infection, However, compared with mammals and insects, the potential function of p38 MAPK from Chinese shrimp (Fenneropenaeus chinensis) in response to viruses and bacterial infection is limited. In the study, the immune responses of four genes MKK3, MKK4, p38 and ATF-2 from F. chinensis were investigated in defending against white spot syndrome virus (WSSV), Vibrio anguillarum (V. anguillarum) and Staphylococcus aureus (S. aureus) infection. Results demonstrated that the expression levels of these four genes were apparently modulated in hemocytes and gills when shrimp were stimulated by WSSV or bacteria, particularly at 3-24 h after infection. MKK3, p38 and ATF-2 were most sensitive to V. anguillarum (Gram-negative bacteria), followed by WSSV and S. aureus (Gram-positive bacteria), while MKK4 gene was most sensitive to S. aureus, followed by WSSV and V. anguillarum. Knockdown of Fcp38 by RNA interference (RNAi) resulted in a reduction in the expression of FcMKK3 and FcATF-2. The results indicate that p38MAPK signaling pathway plays a role in defending against viral and bacterial infections in F. chinensis.

  • 相关文献

[1]Cloning of Hsp21 gene and its expression in Chinese shrimp Fenneropenaeus chinensis in response to WSSV challenge. Gao, Huan,Lai, Xiaofang,Yan, Binlun,Gao, Huan,Kong, Jie,Wang, Weiji,Meng, Xianhong,Cai, Shengli. 2014

[2]Quantitative analysis of temperature, salinity and pH on WSSV proliferation in Chinese shrimp Fenneropenaeus chinensis by real-time PCR. Gao, Huan,Kong, Jie,Li, Zhanjun,Xiao, Guangxia,Meng, Xianhong,Gao, Huan.

[3]BIRC7 gene in channel catfish (Ictalurus punctatus): Identification and expression analysis in response to Edwardsiella tarda, Streptococcus iniae and channel catfish Hemorrhage Reovirus. Li, Min,Wang, Qi-Long,Chen, Song-Lin,Sha, Zhen-Xia,Li, Min,Liu, Yang.

[4]溶藻弧菌用于对虾益生菌的效果评价. 宋晓玲. 2009

[5]不同饵料组合对中国对虾幼体WSSV携带量及存活率的影响. 肖广侠,孟宪红,孔杰,曹宝祥,刘宁,张庆文,罗坤,李战军. 2013

[6]中国对虾抗病性状遗传标记筛选及遗传多样性分析. 李素红,张天时,孔杰,孟宪红. 2009

[7]白斑综合征病毒感染凡纳滨对虾(Litopenaeus vannamei)TRx、LvP38、CAT、POD基因的表达. 刘鹏飞,刘庆慧,吴垠,黄倢. 2015

[8]白斑综合征病毒2014年中国毒株变异区的序列比较. 孙新颖,万晓嫒,刘庆慧,黄倢. 2016

[9]检测对虾白斑综合症病毒(WSSV)与宿主细胞结合的荧光素标记法. 冯书营,黄倢,张仕璀. 2004

[10]2013年中国典型对虾养殖区白斑综合征病毒流行株高变异区序列的分析比较. 孙新颖,万晓媛,刘庆慧,黄倢. 2016

[11]人工培育对虾苗种体内可培养细菌数量及组成分析. 张晓静,宋晓玲,万晓媛,杨冰,黄倢. 2016

[12]聚β-羟基丁酸酯对凡纳滨对虾抗WSSV能力及免疫基因表达量的影响. 邓康裕,孔杰,孟宪红,罗坤,栾生,曹宝祥,刘宁. 2015

[13]饲料中添加复合芽孢杆菌对凡纳滨对虾抗病毒感染能力及抗病基因表达的影响. 孙博超,杨运楷,李玉宏,宋晓玲,黄倢. 2019

[14]酵母双杂交系统用于WSSV粘附蛋白VP37相关蛋白基因的研究. 张莉,黄倢,戴继勋. 2005

[15]2017年中国部分地区白斑综合征病毒高变异区的序列分析. 刘晓娉,孙新颖,刘庆慧,万晓媛,黄倢. 2019

[16]克氏原螯虾自噬相关基因PcAtg2的克隆及其在白斑综合征病毒胁迫下的表达分析. 祝孟茹,问露洁,占铭,公洁,席昌俊,闻海波,沈怀舜. 2023

[17]2016—2017年我国部分地区白斑综合征病毒wsv006的变异分析. 蔡苗,刘庆慧,万晓媛,黄倢. 2018

[18]真核表达载体pcDNA3.1(+)-vp28的构建及其在细胞中的表达. 姜坤,黄健,张峥,成君军,石正丽. 2010

[19]2015年中国典型对虾养殖区WSSV流行株高变异区序列的分析比较. 秦梦雪,孙新颖,万晓媛,刘庆慧,黄倢. 2018

[20]对虾WSSV人工感染螯虾及其检测. 莫照兰,雷质文,杨冰,黄倢,张培军. 2002

作者其他论文 更多>>