The impact of tetrodotoxin (TTX) on the gut microbiome in juvenile tiger pufferfish, Takifugu rubripes

Author:

Wassel Mai A.,Makabe-Kobayashi Yoko,Iqbal Md Mehedi,Takatani Tomohiro,Sakakura Yoshitaka,Hamasaki Koji

Abstract

AbstractTetrodotoxin (TTX) is a potent neurotoxin that accumulates in Takifugu rubripes, commonly known as pufferfish, through the ingestion of TTX-bearing organisms as part of their food chain. Although researchers believe that pufferfish use TTX to relieve stress, data are not currently available on how TTX affects the gut microbiota of pufferfish. To address this gap, our study aimed to investigate whether administering TTX to fish could alter their gut microbiota and overall health under various salinity conditions, including 30.0 ppt, 8.5 ppt, and 1.7 ppt salinity, which represent full-strength, isosmotic, and low-salinity stress, respectively. We analyzed the effect of TTX ingestion on the community structure, core microbiome, and metabolic capabilities of the gut microbiome using high-throughput sequencing technologies. The predominant bacterial taxa within the gut microbiome were Firmicutes (21–85%), Campilobacterota (2.8–67%), Spirochaetota (0.5–14%), and Proteobacteria (0.7–9.8%), with Mycoplasma, uncultured Arcobacteraceae, Brevinema, Vibrio, Rubritalea, and uncultured Pirellulaceae as core genera. Our findings indicated that the impact of TTX on high-abundance genera at 30.0 ppt and 8.5 ppt salinity levels was negligible, indicating their stability and resilience to TTX ingestion. However, at 1.7 ppt, TTX-fed fish showed a significant increase in uncultured Arcobacteraceae. Furthermore, our analysis of TTX-fed fish revealed taxonomic alterations in low-abundance taxa, which altered the predicted functions of the gut microbiota at all salinity levels. These results suggest that TTX administration could cause subtle effects on the metabolic functions of gut microbial communities. Overall, our study provides insights into the complex relationship between a TTX-accumulating animal, T. rubripes, and its gut microbiota.

Funder

Interdisciplinary Collaborative Research Program of the Atmosphere and Ocean Research Institute, The University of Tokyo.

Publisher

Springer Science and Business Media LLC

Reference116 articles.

1. Bucciarelli, G. M. et al. From poison to promise: The evolution of tetrodotoxin and its potential as a therapeutic. Toxins 13, 517 (2021).

2. Lago, J., Rodríguez, L., Blanco, L., Vieites, J. & Cabado, A. Tetrodotoxin, an extremely potent marine neurotoxin: distribution, toxicity, origin and therapeutical uses. Mar. Drugs 13, 6384–6406 (2015).

3. Ahasan, H. A. et al. Paralytic complications of puffer fish (tetrodotoxin) poisoning. Singap. Med. J. 45, 73–74 (2004).

4. Lipsius, M. R., Siegman, M. J. & Kao, C. Y. Direct relaxant actions of procaine and tetrodotoxin on vascular smooth muscle. J. Pharmacol. Exp. Ther. 164, 60–74 (1968).

5. Noguchi, T., Arakawa, O. & Takatani, T. TTX accumulation in pufferfish. Comp. Biochem. Physiol. Part D: Genom. Proteom. 1, 145–152 (2006).

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