Tibet plateau probiotic provides protection for heavy metals toxicity by the gut microbiota

Published in Microbiology
Tibet plateau probiotic provides protection for heavy metals toxicity by the gut microbiota

Share this post

Choose a social network to share with, or copy the shortened URL to share elsewhere

This is a representation of how your post may appear on social media. The actual post will vary between social networks
Tibet Plateau

Soil heavy metals pollution is a global crisis that human faces in the 21st century. The accumulation of heavy metal in crops caused health problems and aroused wide concern. The best known treatment methods for soil heavy metals pollution include phytoremediation, physical-chemical technology, and microbial technology. However, despite today's well-developed mitigation strategies for soil heavy metals pollution, their efficiency is not as high as desired. 

“If the mountain will not come to Muhammad, then Muhammad must go to the mountain.” arises from the story of Muhammad. Francis Bacon, 1625 

We know that several probiotics play an important role in detoxification of ingested heavy metals in both human and murine models. Based on this, we proposed a novel approach against heavy metals contamination, named Gut Remediation. Compared to the traditional heavy metal remediation technologies, gut remediation can be easily obtained by functional probiotics with low-cost in the process of practical application in the future.

Nevertheless, the number of probiotic strains that colonize the gastrointestinal tract has been reported to extremely limited, hence, how the restricted number of probiotics exert their influence to achieve protective effects against heavy metals pollutants aroused our interests. The gut microbiota is the first line of defense against ingested environmental xenobiotics and express some heavy metals-detoxifying genes such as glutathione. So all the microorganisms living in the gut can somehow influence the mitigation effects of heavy metals toxicity in the process of probiotics intervention.

Chromium (Cr) is an omnipresent environmental toxic contaminant and is mainly present in trivalent (Ⅲ) or hexavalent (Ⅵ) forms. Cr(VI) can be easily absorbed by living cells and is a highly hazardous form that causes health problems. Cr(VI) can be reduced to Cr(III), which is poorly absorbed and less toxic. Oxidative stress is one of the key features of heavy metals toxicity. Imbalance between the production of free radicals and generation of antioxidants caused by oxidative stress causes damage to important biomolecules and cells, with potential impact on the whole organism. Tibet plateau probiotic BT36 have strong antioxidant ability attributing to its average 4000 meters height and 6500 MJ/M2 solar radiation.

In this study, we identified some healthy features in mice. To this end, we analyzed 16S rRNA sequencing and metatranscriptome sequencing data from the feces of mice models treated with BT36 and Cr(VI). The gut microbiota composition in different groups were observed to be closely associated with different degrees of oxidative stress. With the help of these finding, we also tested the genes and enzymes in gut microbiota involved in Cr(VI) remediation by screening the different expressed genes. In addition, some genes with unknown function were experimentally demonstrated to be highly tolerant to Cr(VI) and reduce Cr(VI) to Cr(Ⅲ) in vitro. Taken together, BT36 increased the antioxidant defense and Cr(VI)-reduction ability of the gut microbiota by upregulating the expression of relevant genes.

Please sign in or register for FREE

If you are a registered user on Research Communities by Springer Nature, please sign in

Subscribe to the Topic

Life Sciences > Biological Sciences > Microbiology

Related Collections

With collections, you can get published faster and increase your visibility.

Biology of reproduction

For this Collection, we encourage submissions that push forward our understanding of reproduction and its impact on offspring in both model organisms and human studies.

Publishing Model: Open Access

Deadline: Jul 10, 2024