Comparative transcriptome reveals the thermal stress response differences between Heilongjiang population and Xinjiang population of Lota lota

Author(s):  
Fangrui Lou ◽  
Manhong Liu ◽  
Zhiqiang Han ◽  
Tianxiang Gao
2021 ◽  
Vol 96 ◽  
pp. 102859
Author(s):  
Sayed Haidar Abbas Raza ◽  
Sameh A. Abdelnour ◽  
Aya I.M. Dhshan ◽  
Abdallah A. Hassanin ◽  
Ahmed E. Noreldin ◽  
...  

2017 ◽  
Vol 83 ◽  
pp. 5
Author(s):  
Noam Meiri ◽  
Tatiana Kisliouk ◽  
Tomer Cramer ◽  
Tali Rosenberg

2019 ◽  
Author(s):  
Carly D. Kenkel ◽  
Veronique J.L. Mocellin ◽  
Line K. Bay

AbstractThe mechanisms resulting in the breakdown of the coral symbiosis once the process of bleaching has been initiated remain unclear. Distinguishing symbiont loss from the abiotic stress response may shed light on the cellular and molecular pathways involved in each process. This study examined physiological changes and global gene expression patterns associated with white patch syndrome (WPS) in P. lobata, which manifests in localized bleaching independent of thermal stress. In addition, a meta-analysis of global gene expression studies in other corals and anemones was used to contrast differential regulation as a result of abiotic stress from expression patterns correlated with symbiotic state. Symbiont density, chlorophyll a content, holobiont productivity, instant calcification rate, and total host protein content were uniformly reduced in WPS relative to healthy tissue. While expression patterns associated with WPS were secondary to fixed effects of source colony, specific functional enrichments suggest that the viral infection putatively giving rise to this condition affects symbiont rather than host cells. The meta-analysis revealed that expression patterns in WPS-affected tissues were significantly correlated with prior studies examining short-term thermal stress responses. This correlation was independent of symbiotic state, as the strongest correlations were found between WPS adults and both symbiotic adult and aposymbiotic coral larvae experiencing thermal stress, suggesting that the majority of expression changes reflect a non-specific stress response. Across studies, the magnitude and direction of expression change among particular functional enrichments suggests unique responses to stressor duration, and highlights unique responses to bleaching in an anemone model which engages in a non-obligate symbiosis.


Gene ◽  
2013 ◽  
Vol 532 (2) ◽  
pp. 230-235 ◽  
Author(s):  
Rajib Deb ◽  
Basavaraj Sajjanar ◽  
Umesh Singh ◽  
Sushil Kumar ◽  
M.P. Brahmane ◽  
...  

2013 ◽  
Vol 62 ◽  
pp. 717-724 ◽  
Author(s):  
Qingsong Wang ◽  
Haodong Chen ◽  
Yu Wang ◽  
Jinhua Sun

2021 ◽  
Author(s):  
Andrea N. Chan ◽  
Luis A. González-Guerrero ◽  
Roberto Iglesias-Prieto ◽  
Elizabeth M. Burmester ◽  
Randi D. Rotjan ◽  
...  

AbstractScleractinian corals form the foundation of coral reefs by secreting skeletons of calcium carbonate. Their intracellular algal symbionts (Symbiodiniaceae) translocate a large proportion of photosynthate to the coral host, which is required to maintain high rates of calcification. Global warming is causing dissociation of coral host and algal symbiont, visibly presented as coral bleaching. Despite decades of study, the precise mechanisms of coral bleaching remain unknown. Separating the thermal stress response of the coral from the algal symbiont is key to understanding bleaching in tropical corals. The facultatively symbiotic northern star coral, Astrangia poculata, naturally occurs as both symbiotic and aposymbiotic (lacking algal symbionts) polyps – sometimes on the same coral colony. Thus, it is possible to separate the heat stress response of the coral host alone from the coral in symbiosis with its symbiont Breviolum psygmophilum. Using replicate symbiotic and aposymbiotic ramets of A. poculata, we conducted a chronic heat stress experiment to increase our understanding of the cellular mechanisms resulting in coral bleaching. Sustained high temperature stress resulted in photosynthetic dysfunction in B. psygmophilum, including a decline in maximum photosynthesis rate, maximum photochemical efficiency, and the absorbance peak of chlorophyll a. Interestingly, the metabolic rates of symbiotic and aposymbiotic corals were differentially impacted. RNAseq analysis revealed more differentially expressed genes between heat-stressed and control aposymbiotic colonies than heat-stressed and control symbiotic colonies. Notably, aposymbiotic colonies increased the expression of inflammation-associated genes such as nitric oxide synthases. Unexpectedly, the largest transcriptional response was observed between heat-stressed and control B. psygmophilum, including genes involved in photosynthesis, response to oxidative stress, and meiosis. Thus, it appears that the algal symbiont suppresses the immune response of the host, potentially increasing the vulnerability of the host to pathogens. The A. poculata-B. psygmophilum symbiosis provides a tractable model system for investigating thermal stress and immune challenge in scleractinian corals.


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