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Review

Gut microbiota: a non-target victim of pesticide-induced toxicity

ORCID Icon, ORCID Icon, ORCID Icon, ORCID Icon & ORCID Icon
Article: 2187578 | Received 15 Sep 2022, Accepted 01 Mar 2023, Published online: 15 Mar 2023
 

ABSTRACT

The human gut microbiota can be potentially disrupted due to exposure of various environmental contaminants, including pesticides. These contaminants enter into non-target species in multiple ways and cause potential health risks. The gut microbiota-derived metabolites have a significant role in maintaining the host’s health by regulating metabolic homeostasis. An imbalance in this homeostasis can result in the development of various diseases and their pathogenesis. Pesticides have hazardous effects on the host’s gut microbiota, which is evident in a few recent studies. Therefore, there is an urgent need to explore the effect of pesticide on gut microbiota-mediated metabolic changes in the host, which may provide a better understanding of pesticide-induced toxicity. The present review summarizes the pesticide-induced effects on gut microbiota, which in turn, induces changes in the release of their secondary metabolites that could lead to various host health effects.

Acknowledgments

Figures are created with BioRender.com.

Disclosure statement

No potential conflict of interest was reported by the author(s).

Abbreviations

PCP=

Pentachlorophenol

CPF=

chlorpyrifos

HCH=

b-hexachlorohexane

DDT=

p’p’ dichlorodiphenyltrichloroethane

p’p’DDE=

p’p’ dechlorodiphenyldichloro-ethylene

HCH=

hexachlorocyclohexane

OCPs=

Organochlorines pesticides

Tlr4=

Toll-like receptor 4

PAH=

polycyclic aromatic hydrocarbon

PCB=

polychlorinated biphenyl

POPs=

persistent organic pollutants

TMAO=

trimethylamine oxide

Fmo3=

flavin-containing monooxygenase 3

LPS=

lipopolysaccharides

TMA=

trimethylamine

SCFAs=

Short-chain fatty acids

BA=

bile acids

PCP=

Pentachlorophenol

CBZ=

methyl 2-benzimidazolecarbamate

IMZ=

Imazalil

CFTR=

cystic fibrosis transmembrane conductance regulator

PM=

Propamocarb

FXR=

farnesoid X receptor

GPCRs=

G-protein coupled receptors

AHR=

aryl hydrocarbon receptor

IBD=

inflammatory bowel disease

β-MCA=

β – Muricholic acid

Credit authorship contribution statement

T.S. Writing – original draft preparation, review, and editing, N.S.N. Writing, review, editing, and visualization. RP. Review and editing, S.K.B and S.R. Conceptualization review and editing, all authors have read and agreed to the published version of the manuscript.

Additional information

Funding

The authors obtained funding support for this manuscript, in part, from the National Institutes of Health [R01 CA247763].