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微碎裂诱导珊瑚加速生长的机制及潜在免疫权衡。

Mechanisms and potential immune tradeoffs of accelerated coral growth induced by microfragmentation.

机构信息

Smith College, Northampton, Massachusetts, United States.

Mote Marine Laboratory, Summerland Key, Florida, USA.

出版信息

PeerJ. 2022 Mar 29;10:e13158. doi: 10.7717/peerj.13158. eCollection 2022.

DOI:10.7717/peerj.13158
PMID:35368334
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8973463/
Abstract

Microfragmentation is the act of cutting corals into small pieces (~1 cm) to accelerate the growth rates of corals relative to growth rates observed when maintaining larger-sized fragments. This rapid tissue and skeletal expansion technique offers great potential for supporting reef restoration, yet the biological processes and tradeoffs involved in microfragmentation-mediated accelerated growth are not well understood. Here we compared growth rates across a range of successively smaller fragment sizes in multiple genets of reef-building corals, and . Our results confirm prior findings that smaller initial sizes confer accelerated growth after four months of recovery in a raceway. transcript levels associated with growth rate include genes encoding carbonic anhydrase and glutamic acid-rich proteins, which have been previously implicated in coral biomineralization, as well as a number of unannotated transcripts that warrant further characterization. Innate immunity enzyme activity assays and gene expression results suggest a potential tradeoff between growth rate after microfragmentation and immune investment. Microfragmentation-based restoration practices have had great success on Caribbean reefs, despite widespread mortality among wild corals due to infectious diseases. Future studies should continue to examine potential immune tradeoffs throughout the microfragmentation recovery period that may affect growout survival and disease transmission after outplanting.

摘要

微碎片是将珊瑚切成小块(~1 厘米)的行为,以加速珊瑚的生长速度,相对于观察到的较大碎片的生长速度。这种快速组织和骨骼扩张技术为支持珊瑚礁恢复提供了巨大的潜力,但微碎片介导的加速生长所涉及的生物学过程和权衡尚不清楚。在这里,我们比较了多个造礁珊瑚种系中一系列逐渐变小的碎片大小的生长率,以及 。我们的结果证实了先前的发现,即在赛道中恢复四个月后,较小的初始大小会带来更快的生长。与生长速率相关的 转录本水平包括编码碳酸酐酶和富含谷氨酸的蛋白质的基因,这些基因先前与珊瑚生物矿化有关,以及许多未经注释的转录本,值得进一步表征。先天免疫酶活性测定和基因表达结果表明,微碎片后生长速度和免疫投资之间可能存在权衡。尽管由于传染病,加勒比海珊瑚礁的野生珊瑚广泛死亡,但基于微碎片的恢复实践取得了巨大成功。未来的研究应该继续在微碎片恢复期间检查潜在的免疫权衡,这可能会影响种植后的生长成活率和疾病传播。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/576f/8973463/33e2e0715425/peerj-10-13158-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/576f/8973463/48b65a113596/peerj-10-13158-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/576f/8973463/ff052435498c/peerj-10-13158-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/576f/8973463/c2c6e910df2d/peerj-10-13158-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/576f/8973463/bc939c92f7e6/peerj-10-13158-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/576f/8973463/33e2e0715425/peerj-10-13158-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/576f/8973463/48b65a113596/peerj-10-13158-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/576f/8973463/ff052435498c/peerj-10-13158-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/576f/8973463/c2c6e910df2d/peerj-10-13158-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/576f/8973463/bc939c92f7e6/peerj-10-13158-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/576f/8973463/33e2e0715425/peerj-10-13158-g005.jpg

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