A shift away from mutualism under food-deprived conditions in an anemone-dinoflagellate association

Author:

Peng Shao-En12,Moret Alessandro3,Chang Cherilyn1,Mayfield Anderson B.145,Ren Yu-Ting2,Chen Wan-Nan U.6,Giordano Mario37,Chen Chii-Shiarng12

Affiliation:

1. National Museum of Marine Biology and Aquarium, Pingtung, Taiwan

2. Graduate Institute of Marine Biology, National Dong Hwa University, Pingtung, Taiwan

3. Dipatimento di Scienze della Vita e dell’Ambiente, Università Politecnica delle Marche, Ancona, Italy

4. Cooperative Institute for Marine and Atmospheric Sciences Studies, University of Miami, Miami, FL, United States of America

5. Atlantic Oceanographic and Meteorological Laboratory, National Oceanic and Atmospheric Administration, Miami, FL, United States of America

6. Department of Biological Science and Technology, I-Shou University, Kaohsiung, Taiwan

7. Institute of Microbiology ASCR, Algatech, Trebon, Czech Republic

Abstract

The mutualistic symbiosis between anthozoans and intra-gastrodermal dinoflagellates of the family Symbiodiniaceae is the functional basis of all coral reef ecosystems, with the latter providing up to 95% of their fixed photosynthate to their hosts in exchange for nutrients. However, recent studies of sponges, jellyfish, and anemones have revealed the potential for this mutualistic relationship to shift to parasitism under stressful conditions. Over a period of eight weeks, we compared the physiological conditions of both inoculated and aposymbiotic anemones (Exaiptasia pallida) that were either fed or starved. By the sixth week, both fed groups of anemones were significantly larger than their starved counterparts. Moreover, inoculated and starved anemones tended to disintegrate into “tissue balls” within eight weeks, and 25% of the samples died; in contrast, starved aposymbiotic anemones required six months to form tissue balls, and no anemones from this group died. Our results show that the dinoflagellates within inoculated anemones may have posed a fatal metabolic burden on their hosts during starvation; this may be because of the need to prioritize their own metabolism and nourishment at the expense of their hosts. Collectively, our study reveals the potential of this dynamic symbiotic association to shift away from mutualism during food-deprived conditions.

Funder

Taiwan’s Ministry of Science and Technology

Publisher

PeerJ

Subject

General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3