Susceptibility of Lymantria dispar to Beauveria bassiana under short-term Cd stress: Humoral immunostimulation cannot offset cellular immunotoxicity

被引:0
|
作者
Zhang, Aoying [1 ,2 ]
Li, Yaning [1 ,2 ]
Tan, Mingtao [1 ,2 ]
Wang, Ying [1 ,2 ]
He, Yubin [1 ,2 ]
Yan, Shanchun [1 ,2 ]
Jiang, Dun [1 ,2 ]
机构
[1] Northeast Forestry Univ, Sch Forestry, Harbin 150040, Peoples R China
[2] Northeast Forestry Univ, Minist Educ, Key Lab Sustainable Forest Ecosyst Management, Harbin 150040, Peoples R China
基金
中国国家自然科学基金;
关键词
Innate immunity; Immunity modification; Heavy metals; Hormesis; Gloverin; HEAVY-METAL POLLUTION; ACTIVATION;
D O I
10.1016/j.jhazmat.2024.136037
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Heavy metal is a serious environmental pollutant with all kinds of biotoxic effects. The immunomodulatory effects of Cd stress on Lymantria dispar larvae and its underlying mechanisms were investigated. The susceptibility of Cd-treated larvae to Beauveria bassiana (Bb) was significantly increased by 27.50 %. The hemocyte count, melanization, encapsulation activities, and expression levels of related regulatory genes (e.g. PPO1 and DSCAM) ) in the Cd and Cd+Bb +Bb groups were markedly lower than those in CK and CK+Bb +Bb groups. Hemocyte compensation through the apoptosis inhibitor significantly increased the melanization, encapsulation, and the survival rate of larvae in the Cd+Bb +Bb group by 100.00 %, 74.03 %, and 18.33 %, respectively. The expression of signal transduction and effector genes (e.g. Gloverin) ) was significantly elevated in Cd-treated larvae both before and after Bb infection. Silencing Gloverin resulted in a 9.17 % increase in susceptibility of Cd-treated larvae to Bb. Cd exposure induced humoral immunostimulation in larvae through the CncC-Gloverin pathway, as evidenced by that silencing CncC resulted in a 71.07 % decrease in Gloverin expression and a 19.73 % increase in larval mortality in Cd+Bb +Bb group. Overall, the humoral immunostimulation induced by Cd stress in L. dispar larvae were insufficient to counteract the cellular immunotoxicity during Bb infection.
引用
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页数:15
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