Chinese Journal of Applied Ecology ›› 2022, Vol. 33 ›› Issue (9): 2572-2584.doi: 10.13287/j.1001-9332.202209.031
• Reviews • Previous Articles Next Articles
WANG Tao, CHENG Ke-ke, CAI Zhong-hua, ZHOU Jin*
Received:
2021-07-12
Accepted:
2022-05-09
Online:
2022-09-15
Published:
2023-03-15
WANG Tao, CHENG Ke-ke, CAI Zhong-hua, ZHOU Jin. Research advances in communication interactions among the symbionts of “bacteria-zooxanthellae-coral”[J]. Chinese Journal of Applied Ecology, 2022, 33(9): 2572-2584.
Add to citation manager EndNote|Ris|BibTeX
URL: https://www.cjae.net/EN/10.13287/j.1001-9332.202209.031
[1] Zoccola D, Ounais N, Barthelemy D, et al. The World Coral Conservatory (WCC): A Noah’s ark for corals to support survival of reef ecosystems. PLoS Biology, 2020, 18(9): e3000823 [2] Sorokin YI. Coral Reef Ecology. Berlin: Springer-Verlag, 1993: 1-3 [3] Oppen MJHV, Blackall LL. Coral microbiome dynamics, functions and design in a changing world. Nature Reviews Microbiology, 2019, 17: 557-567 [4] Peixoto RS, Rosado PM, Assis LDCD, et al. Beneficial microorganisms for corals (BMC): Proposed mechanisms for coral health and resilience. Frontiers in Microbiology, 2017, 8: 341 [5] 汤开浩, 王嫣, 王晓雪. 造礁珊瑚共附生微生物信号分子的研究进展. 中国科学: 地球科学, 2019, 49(5): 753-764 [6] 林姿君, 杜小鹏, 曾艳华, 等. 珊瑚共生细菌稳定性调节机制研究进展. 应用与环境生物学报, 2020, 26(4): 857-866 [7] Rosset SL, Oakley CA, Ferrior-Pagès C, et al. The molecular language of the cnidarian-dinoflagellate symbiosis. Trends in Microbiology, 2020, 29: 320-333 [8] Matthews JL, Crowder CM, Oakley CA, et al. Optimal nutrient exchange and immune responses operate in partner specificity in the cnidarian-dinoflagellate symbiosis. Proceedings of the National Academy of Sciences of the United States of America, 2017, 114: 13194-13199 [9] Kaiser D, Losick R. How and why bacteria talk to each other. Cell, 1993, 73: 873-885 [10] Padder SA, Prasad R, Shah AH. Quorum sensing: A less known mode of communication among fungi. Microbiological Research, 2018, 210: 51-58 [11] Cude WN, Buchan A. Acyl-homoserine lactone-based quorum sensing in the Roseobacter clade: Complex cell-to-cell communication controls multiple physiologies. Frontiers in Microbiology, 2013, 4: 336, doi: 10.3389/fmicb.2013.00336 [12] 林姿君. 鹿角珊瑚中群体感应细菌的筛选及其对白化的介导作用. 硕士论文. 北京: 清华大学, 2019 [13] Tait K, Hutchison Z, Thompson FL, et al. Quorum sensing signal production and inhibition by coral-associated vibrios. Environmental Microbiology Reports, 2010, 2: 145-150 [14] Certner RH, Vollmer SV. Evidence for autoinduction and quorum sensing in white band disease causing microbes on Acropora cervicornis. Scientific Reports, 2015, 5(1): 11134, doi: 10.1038/srep11134 [15] Zhou J, Lin ZJ, Cai ZH, et al. Opportunistic bacteria use quorum sensing to disturb coral symbiotic communities and mediate the occurrence of coral bleaching. Environmental Microbiology, 2020, 22: 1944-1962 [16] Munn CB. The role of Vibrios in diseases of corals. Microbiology Spectrum, 2015, 3: VE-0006-2014 [17] Tello E, Castellanos L, Arévalo-Ferro C, et al. Disruption in quorum-sensing systems and bacterial biofilm inhibition by cembranoid diterpenes isolated from the octocoral Eunicea knighti. Journal of Natural Products, 2012, 75: 1637-1642 [18] Certner RH, Vollmer SV. Inhibiting bacterial quorum sensing arrests coral disease development and disease-associated microbes. Environmental Microbiology, 2018, 20: 645-657 [19] Alagely A, Krediet CJ, Ritchie KB, et al. Signaling mediated cross-talk modulates swarming and biofilm formation in a coral pathogen Serratia marcescens. The ISME Journal, 2011, 5: 1609-1620 [20] Teplitski M, Warriner K, Bartz J, et al. Untangling metabolic and communication networks: Interactions of Enterics with phytobacteria and their implications in produce safety. Trends in Microbiology, 2011, 19: 121-127 [21] Skindersoe ME, Ettinger-Epstein P, Rasmussen TB, et al. Quorum sensing antagonism from marine organisms. Marine Biotechnology, 2008, 10: 56-63 [22] Rajamani S, Bauer WD, Robinson JB, et al. The vitamin riboflavin and its derivative lumichrome activate the LasR bacterial quorum-sensing receptor. Molecular Plant-Microbe Interactions, 2008, 21: 1184-1192 [23] Cleo P, Christian T, Sylvain F, et al. Host modification of a bacterial quorum-sensing signal induces a phenotypic switch in bacterial symbionts. Proceedings of the National Academy of Sciences of the United States of America, 2017, 114: E8488-E8497 [24] Van DWJAJM , Allemand D, Ferrier-Pagès C. Host-microbe interactions in octocoral holobionts-recent advances and perspectives. Microbiome, 2018, 6: 64 [25] Wheeler GL, Tait K, Taylor A, et al. Acylhomoserine lactones modulate the settlement rate of zoospores of the marine alga Ulva intestinalis via a novel chemokinetic mechanism. Plant, Cell and Environment, 2006, 29: 608-618 [26] Zimmer BL, May AL, Bhedi CD, et al. Quorum sensing signal production and microbial interactions in a polymicrobial disease of corals and the coral surface mucopolysaccharide layer. PLoS One,2014, 9(9): e108541 [27] Raina JB, Tapiolas D, Forêt S, et al. DMSP biosynthesis by an animal and its role in coral thermal stress response. Nature, 2013, 502: 677-680 [28] Tout J, Jeffries TC, Petrou K, et al. Chemotaxis by natural populations of coral reef bacteria. The ISME Journal, 2015, 9: 1764-1777 [29] Raina JB, Dinsdale EA, Willis BL, et al. Do the organic sulfur compounds DMSP and DMS drive coral microbial associations? Trends in Microbiology, 2010, 18: 101-108 [30] Garren M, Son K, Raina JB, et al. A bacterial pathogen uses dimethylsulfoniopropionate as a cue to target heat-stressed corals. The ISME Journal, 2014, 8: 999-1007 [31] Patra SK, Samaddar S, Sinha N, et al. Reactive nitrogen species induced catalases promote a novel nitrosative stress tolerance mechanism in Vibrio cholerae. Nitric Oxide-Biology and Chemistry, 2019, 88: 35-44 [32] Wang CY, Wang KL, Qian PY, et al. Antifouling phenyl ethers and other compounds from the invertebrates and their symbiotic fungi collected from the South China Sea. AMB Express, 2016, 6: 1-10 [33] Pham TM, Wiese J, Wenzel-Storjohann A, et al. Diversity and antimicrobial potential of bacterial isolates associated with the soft coral Alcyonium digitatum from the Baltic Sea. Antonie Van Leeuwenhoek, 2016, 109: 105-119 [34] Elahwany AMD, Ghozlan HA, Elsharif HA, et al. Phylogenetic diversity and antimicrobial activity of marine bacteria associated with the soft coral Sarcophyton glaucum. Journal of Basic Microbiology, 2015, 55: 2-10 [35] Williams GC, Chen JY. Resurrection of the octocorallian genus Antillogorgia for Caribbean species previously assigned to Pseudopterogorgia, and a taxonomic assessment of the relationship of these genera with Leptogorgia (Cnidaria, Anthozoa, Gorgoniidae). Zootaxa, 2012, 3505: 39-52 [36] Karthik L, Li Z. Biosynthesis of antibiotics from microbial symbionts of sponges and corals// Loganathan K, ed. Symbiotic Microbiomes of Coral Reefs Sponges and Corals. Dordrecht: Springer, 2019: 249-261 [37] 杨静明, 杨文聪, 刘亚月, 等. 化学诱导对一株海洋来源土曲霉C23-3次生代谢产物及其生物活性的影响. 微生物学通报, 2019, 46(3): 441-452 [38] 郭秀春, 郑立, 崔志松, 等. 海绵共栖细菌NJ6-3-1基于群体感应调控的抗菌活性. 微生物学通报, 2008, 48(4): 545-550 [39] 周进, 晋慧, 蔡中华. 微生物在珊瑚礁生态系统中的作用与功能. 应用生态学报, 2014, 25(3): 919-930 [40] Seymour JR, Simó R, Ahmed T, et al. Chemoattraction to dimethylsulfoniopropionate throughout the marine microbial food web. Science, 2010, 329: 342-345 [41] Guibert I, Bourdreux F, Bonnard I. et al. Dimethylsulfoniopropionate concentration in coral reef invertebrates varies according to species assemblages. Scientific Reports, 2020, 10: 9922 [42] Geng HF, Belas R. Molecular mechanisms underlying roseobacter-phytoplankton symbioses. Current Opinion in Biotechnology, 2010, 21: 332-338 [43] Davidson SK, Koropatnick TA, Kossmehl R, et al. NO means ‘yes’ in the squid-vibrio symbiosis: Nitric oxide (NO) during the initial stages of a beneficial association. Cellular Microbiology, 2004, 6: 1139-1151 [44] Plate L, Marletta MA. Nitric oxide-sensing H-NOX proteins govern bacterial communal behavior. Trends in Biochemical Sciences, 2013, 38: 566-575 [45] Barry M. Genetic recombination in Rhodopseudomonas capsulata. Proceedings of the National Academy of Sciences of the United States of America, 1974, 71: 971-973 [46] Luo HW, Moran MA. Evolutionary ecology of the marine Roseobacter clade. Microbiology and Molecular Biology Review, 2014, 78: 573-587 [47] Tooba V, Ana PBM, Arthur WSL, et al. Genomic repertoire of Mameliella alba Ep20 associated with Symbiodinium from the endemic coral Mussismilia braziliensis. Symbiosis, 2020, 80: 53-60 [48] Parkinson JE, Tivey TR, Mandelare PE, et al. Subtle differences in symbiont cell surface glycan profiles do not explain species-specific colonization rates in a model cnidarian-algal symbiosis. Frontiers in Microbiology, 2018, 9: 842-854 [49] Kitchen SA, Weis VM. The sphingosine rheostat is involved in the cnidarian heat stress response but not necessarily in bleaching. Journal of Experimental Biology, 2017, 220: 1709-1720 [50] Hambleton EA, Jones VAS, Maegele I, et al. Sterol transfer by atypical cholesterol-binding NPC2 proteins in coral-algal symbiosis. eLife, 2019, 8: e43923 [51] Marangoni LFB, Mies M, Guth AZ, et al. Peroxynitrite generation and increased heterotrophic capacity are linked to the disruption of the coral-dinoflagellate symbiosis in a scleractinian and hydrocoral species. Microorganisms, 2019, 7: 426 [52] Baumgarten S, Cziesielski MJ, Thomas L, et al. Evidence for miRNA-mediated modulation of the host transcriptome in cnidarian-dinoflagellate symbiosis. Molecular Ecology, 2018, 27: 403-418 [53] 杨潇湘, 张蕾, 黄小琴, 等. 基于高通量测序分析大豆和油菜根际微生物群落结构的差异. 应用生态学报, 2019, 30(7): 2345-2351 [54] Varki A. Biological roles of glycans. Glycobiology, 2017, 27: 3-49 [55] Kuniya N, Jimbo M, Tanimoto F, et al. Possible involvement of Tachylectin-2-like lectin from Acropora tenuis in the process of Symbiodinium acquisition. Fisheries Science, 2015, 81: 473-483 [56] Meints RH, Pardy RL. Quantitative demonstration of cell surface involvement in a plant-animal symbiosis: Lectin inhibition of reassociation. Journal of Cell Science, 1980, 43: 239-251 [57] Dennis EA, Norris PC. Eicosanoid storm in infection and inflammation. Nature Reviews Immunology, 2015, 15: 511-523 [58] Niu M, Keller NP. Co-opting oxylipin signals in microbial disease. Cellular Microbiology, 2019, 21: e13025 [59] Deboever E, Deleu M, Mongrand S, et al. Plant-pathogen interactions: Underestimated roles of phyto-oxylipins. Trends in Plant Science, 2020, 25: 22-34 [60] Lõhelaid H, Samel N. Eicosanoid diversity of stony corals. Marine Drugs, 2018, 16(1): 10 [61] Lawson CA, Possell M, Seymour JR, et al. Coral endosymbionts (Symbiodiniaceae) emit species-specific volatilomes that shift when exposed to thermal stress. Scientific Reports, 2019, 9: 17395 [62] Hannun YA, Obeid LM. Sphingolipids and their metabolism in physiology and disease. Nature Reviews Molecular Cell Biology, 2018, 19: 175-191 [63] Rolando M, Escoll P, Nora T, et al. Legionella pneumophila S1P-lyase targets host sphingolipid metabolism and restrains autophagy. Proceedings of the National Academy of Sciences of the United States of America, 2016, 113: 1901-1906 [64] Ali U, Li HH, Wang XM, et al. Emerging roles of sphingolipid signaling in plant response to biotic and abiotic stresses. Molecular Plant, 2018, 11: 1328-1343 [65] Luttgeharm KD, Chen M, Mehra A, et al. Overexpression of arabidopsis ceramide synthases differentially affects growth, sphingolipid metabolism, programmed cell death, and mycotoxin resistance. Plant Physiology, 2015, 169: 1108-1117 [66] Rodriguez-Lanetty M, Phillips WS, Weis VM, et al. Transcriptome analysis of a cnidarian-dinoflagellate mutualism reveals complex modulation of host gene expression. BMC Genomics, 2006, 7: 23 [67] Detournay O, Weis VM. Role of the sphingosine rheostat in the regulation of cnidarian-dinoflagellate symbioses. The Biological Bulletin, 2011, 221: 261-269 [68] Wollam J, Antebi A. Sterol regulation of metabolism, homeostasis, and development. Annual Review of Biochemistry, 2011, 80: 885-916 [69] Baumgarten S, Simakov O, Esherick LY, et al. The genome of Aiptasia, a sea anemone model for coral symbiosis. Proceedings of the National Academy of Sciences of the United States of America, 2015,112: 11893-11898 [70] Dani V, Priouzeau F, Mertz M, et al. Expression patterns of sterol transporters NPC1 and NPC2 in the cnidarian-dinoflagellate symbiosis. Cellular Microbiology, 2017, 19: e12753 [71] Manes S, Real DG, Martinez AC, et al. Pathogens: Raft hijackers. Nature Reviews Immunology, 2003, 3: 557-568 [72] Paul S, Roychoudhury A. Regulation of physiological aspects in plants by hydrogen sulfide and nitric oxide under challenging environment. Physiologia Plantarum, 2020, 168: 374-393 [73] Cortese-Krott MM, Koning A, Kuhnle GGC, et al. The reactive species interactome: Evolutionary emergence, biological significance, and opportunities for redox metabolomics and personalized medicine. Antioxidants and Redox Signaling, 2017, 27: 684-712 [74] Suggett DJ, Smith DJ. Coral bleaching patterns are the outcome of complex biological and environmental networking. Global Chang Biology, 2020, 26: 68-79 [75] Peleg-Grossman S, Melamed-Book N, Levine A, et al. ROS production during symbiotic infection suppresses pathogenesis-related gene expression. Plant Signaling and Behavior, 2012, 7: 409-415 [76] Hawkins TD, Krueger T, Becker S, et al. Differential nitric oxide synthesis and host apoptotic events correlate with bleaching susceptibility in reef corals. Coral Reefs, 2014, 33: 141-153 [77] Weiberg A, Bellinger M, Jin HL, et al. Conversations between kingdoms: Small RNAs. Current Opinion Biotechnology, 2015, 32: 207-215 [78] Xu YJ, Zhu SW, Liu F, et al. Identification of arbuscular mycorrhiza fungi responsive microRNAs and their regulatory network in maize. International Journal of Molecular Sciences, 2018, 19: 1-13 [79] Lin SJ, Cheng SF, Song B, et al. The Symbiodinium kawagutii genome illuminates dinoflagellate gene expression and coral symbiosis. Science, 2015, 350: 691-694 [80] Ware JR, Smith SV, Reaka-Kudla ML. Coral reefs: Sources or sinks of atmospheric CO2? Coral Reefs, 1992, 11: 127-130 [81] Macreadie PI, Anton A, Raven JA, et al. The future of blue carbon science. Nature Communications, 2019, 10: 1-13 [82] 石拓, 郑新庆, 张涵, 等. 珊瑚礁: 减缓气候变化的潜在蓝色碳汇. 中国科学院院刊, 2021, 36(3): 270-278 |
[1] | WANG Jin, ZHOU Guangsheng, HE Qijin, ZHOU Li. Phenological characteristics of net ecosystem carbon exchange of Stipa krylovii steppe in Inner Mongolia, China and its remote sensing monitoring [J]. Chinese Journal of Applied Ecology, 2024, 35(3): 659-668. |
[2] | LIANG Huaqiu, SHEN Menghan, SHAO Ming, YAO Peng. Construction of carbon sequestration ecological network in Linyi City based on supply and demand of ecosystem service [J]. Chinese Journal of Applied Ecology, 2024, 35(3): 759-768. |
[3] | LIANG Shihao, LI Wen, GAO Yu, LIU Baozhu. Correlations between ecosystem service value and landscape ecological risk and its spatial heterogeneity in Jilin Province, China [J]. Chinese Journal of Applied Ecology, 2024, 35(3): 769-779. |
[4] | CAI Lulu, SUN Shoujia, SHI Guangyao, DU Lingtong, NI Xilu, ZHANG Jinsong, MENG Ping. Relationship between negative air ion and PM2.5 in Quercus variabilis under natural conditions [J]. Chinese Journal of Applied Ecology, 2024, 35(2): 347-353. |
[5] | LU Chang, CAI Xueqin, HAO Canshu, LIU Yuzhen, WANG Zhiyu, MA Ya'nan. Ecosystem service tradeoff and synergistic relationship in the Yellow River Delta High-Efficiency Eco-Economic Zone [J]. Chinese Journal of Applied Ecology, 2024, 35(2): 457-468. |
[6] | YU Haixia, WANG Yuxiao. Spatio-temporal variations of ecosystem service value and its spatial heterogeneity mechanism in the Dongjiang River Basin, China [J]. Chinese Journal of Applied Ecology, 2023, 34(9): 2498-2506. |
[7] | QI Yuting, ZHANG Ping, LIU Lei, MA Xuenan, WANG Huan, ZHAO Juan. Multi-scenario optimization of land use structure and prediction of ecosystem service value in Guanzhong Plain urban agglomeration [J]. Chinese Journal of Applied Ecology, 2023, 34(9): 2507-2517. |
[8] | KONG Dongyan, YANG Lingfang, DIAO Jingwen, GUO Peng. Meta-analysis on the effects of nitrogen deposition on soil N2O flux in different habitats [J]. Chinese Journal of Applied Ecology, 2023, 34(8): 2171-2177. |
[9] | XIONG Xinying, MENG Mei. Regionalization and optimization strategy of ecological management in Xinjiang, China based on supply-demand relationship and spatial flow of ecosystem services [J]. Chinese Journal of Applied Ecology, 2023, 34(8): 2237-2248. |
[10] | BA Xiaobo, SUI Xin, LIU Mingda, XIE Hongtu, LIANG Chao, BAO Xuelian. Ecosystem service value of conservation tillage with cover crop-maize intercropping in the black soil region of Northeast China [J]. Chinese Journal of Applied Ecology, 2023, 34(7): 1883-1891. |
[11] | CHEN Honglian, LI Rui, ZHANG Yushan, WU Qinglin, YUAN Jiang, GAO Jiayong. Comparison of ecosystem health in different geomorphic regions of Chishui River Basin, Southwest China [J]. Chinese Journal of Applied Ecology, 2023, 34(7): 1912-1922. |
[12] | HUANG Qingyang, XIE Lihong, CAO Hongjie, WANG Limin, YANG Fan, WANG Jifeng, LIU Yingnan, NI Hongwei. Effects of bacteria on early-stage litter decomposition in Wudalianchi volcanic forest [J]. Chinese Journal of Applied Ecology, 2023, 34(7): 1941-1948. |
[13] | PANG Danbo, WU Mengyao, ZHAO Yaru, YANG Juan, DONG Liguo, WU Xudong, CHEN Lin, LI Xuebin, NI Xilu, LI Jingyao, LIANG Yongliang. Soil microbial community characteristics and the influencing factors at different elevations on the eastern slope of Helan Mountain, Northwest China [J]. Chinese Journal of Applied Ecology, 2023, 34(7): 1957-1967. |
[14] | CHEN Yang, LI Huirong, LI Dongnan, SUN Pengfei, SU Jianghua. Characteristics of net ecosystem exchange and source distribution of Xilinhot grassland, China [J]. Chinese Journal of Applied Ecology, 2023, 34(6): 1509-1516. |
[15] | LI Chenglong, ZHOU Guangsheng, ZHOU Mengzi, ZHOU Li, LIU Jie. Net ecosystem productivity of Panjin Phragmites australis wetland during 1971 to 2020 and its impact factors [J]. Chinese Journal of Applied Ecology, 2023, 34(5): 1331-1340. |
Viewed | ||||||
Full text |
|
|||||
Abstract |
|
|||||