Effect of different temperatures on the expression of the newly characterized heat shock protein 90 (Hsp90) in L3 of Anisakis spp. isolated from Scomber australasicus

被引:21
作者
Chen, Hui-Yu [1 ]
Cheng, Yi-Sheng [1 ]
Grabner, Daniel S. [2 ]
Chang, Shih-Hsin [3 ]
Shih, Hsiu-Hui [1 ]
机构
[1] Natl Taiwan Univ, Dept Life Sci, Taipei 10617, Taiwan
[2] Univ Duisburg Essen, Fac Biol, Dept Aquat Ecol, D-45141 Essen, Germany
[3] Natl Yang Ming Univ, Dept Trop Med, Taipei 11221, Taiwan
关键词
Anisakis pegreffii; Anisakis brevispiculata; Anisakis physeteris; Anisakis paggiae; Hsp90; Temperature resistance; SIMPLEX SENSU-STRICTO; MOLECULAR CHARACTERIZATION; MESSENGER-RNA; NEMATODA ANISAKIDAE; STRESS-RESPONSE; LARVAE; FISH; PEGREFFII; CELL; HEAT-SHOCK-PROTEIN-90;
D O I
10.1016/j.vetpar.2014.09.013
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Anisakid nematodes are distributed worldwide in a wide variety of marine fishes and they are known to cause the zoonotic disease, anisakiasis. The temperature control is commonly applied for prevention and control of anisakiasis. To analyze the cellular response to temperature stress in Anisakis, the heat shock protein 90 (Hsp90) was chosen in the present study, as it plays a key role in many cellular processes and responds to stress conditions such as heat or cold shock. Anisakids were sampled from spotted mackerel Scomber australasicus caught from the coastal waters of Yilan, in northeastern Taiwan (25 degrees N, 121 degrees E). Anisakid nematodes were pre-identified morphologically and later molecularly by PCR-RFLP. In total, we obtained six species of the genus Anisakis, A. typica, A. pegreffii, A. paggiae, A. brevispiculata, A. physeteris, and a recombinant genotype between A. pegreffii and A. simplex sensu stricto. Thereby we provide new host and locality records for A. paggiae, A. brevispiculata and A. physeteris. The Hsp90 genes of five species (except the recombinant genotype) were cloned by rapid amplification of cDNA ends (RACE) and their deduced amino acid sequences were further characterized. Quantitative real-time PCR and Western blot analysis were used to examine the expression levels of the Hsp90 in A. pegreffii under different temperature conditions. Quantitative RT-PCR showed that Hsp90 transcript levels increased slightly under heat shock (50 degrees C) treatment, and increased gradually during the first 3 h, and thereafter, returned to its baseline value at 37 degrees C. Under cold shock (4 degrees C) treatment, the mRNA expression of Hsp90 did not change significantly. In addition, we found a clear time-dependent Hsp90 protein expression pattern of A. pegreffii exposed to high temperature. Our results suggest that the mRNA and protein expression patterns of Hsp90 are related to the temperature, and are especially significantly increased under heat stress. (C) 2014 Published by Elsevier B.V.
引用
收藏
页码:540 / 550
页数:11
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