» Articles » PMID: 32019196

Distribution of Medically Relevant Antibiotic Resistance Genes and Mobile Genetic Elements in Soils of Temperate Forests and Grasslands Varying in Land Use

Overview
Journal Genes (Basel)
Publisher MDPI
Date 2020 Feb 6
PMID 32019196
Citations 2
Authors
Affiliations
Soon will be listed here.
Abstract

Antibiotic-resistant pathogens claim the lives of thousands of people each year and are currently considered as one of the most serious threats to public health. Apart from clinical environments, soil ecosystems also represent a major source of antibiotic resistance determinants, which can potentially disseminate across distinct microbial habitats and be acquired by human pathogens via horizontal gene transfer. Therefore, it is of global importance to retrieve comprehensive information on environmental factors, contributing to an accumulation of antibiotic resistance genes and mobile genetic elements in these ecosystems. Here, medically relevant antibiotic resistance genes, class 1 integrons and IncP-1 plasmids were quantified via real time quantitative PCR in soils derived from temperate grasslands and forests, varying in land use over a large spatial scale. The generated dataset allowed an analysis, decoupled from regional influences, and enabled the identification of land use practices and soil characteristics elevating the abundance of antibiotic resistance genes and mobile genetic elements. In grassland soils, the abundance of the macrolide resistance gene as well as the sulfonamide resistance gene was positively correlated with organic fertilization and the abundance of , conferring resistance to different aminoglycosides, increased with mowing frequency. With respect to forest soils, the beta-lactam resistance gene was significantly correlated with fungal diversity which might be due to the fact that different fungal species can produce beta-lactams. Furthermore, except and , the analyzed antibiotic resistance genes as well as IncP-1 plasmids and class-1 integrons were detected less frequently in forest soils than in soils derived from grassland that are commonly in closer proximity to human activities.

Citing Articles

A database on the abundance of environmental antibiotic resistance genes.

Xu W, Pan Z, Wu Y, An X, Wang W, Adamovich B Sci Data. 2024; 11(1):250.

PMID: 38413616 PMC: 10899624. DOI: 10.1038/s41597-024-03084-8.


Fate of Horizontal-Gene-Transfer Markers and Beta-Lactamase Genes during Thermophilic Composting of Human Excreta.

Werner K, Feyen L, Hubner T, Bruggemann N, Prost K, Grohmann E Microorganisms. 2023; 11(2).

PMID: 36838273 PMC: 9958827. DOI: 10.3390/microorganisms11020308.

References
1.
Wang S, Zhou K, Xiao S, Xie L, Gu F, Li X . A Multidrug Resistance Plasmid pIMP26, Carrying bla, fosA5, bla, and qnrB4 in Enterobacter cloacae. Sci Rep. 2019; 9(1):10212. PMC: 6629617. DOI: 10.1038/s41598-019-46777-6. View

2.
Yergeau E, Sanschagrin S, Maynard C, St-Arnaud M, Greer C . Microbial expression profiles in the rhizosphere of willows depend on soil contamination. ISME J. 2013; 8(2):344-58. PMC: 3906822. DOI: 10.1038/ismej.2013.163. View

3.
Peng S, Feng Y, Wang Y, Guo X, Chu H, Lin X . Prevalence of antibiotic resistance genes in soils after continually applied with different manure for 30 years. J Hazard Mater. 2017; 340:16-25. DOI: 10.1016/j.jhazmat.2017.06.059. View

4.
Allen H, Donato J, Wang H, Cloud-Hansen K, Davies J, Handelsman J . Call of the wild: antibiotic resistance genes in natural environments. Nat Rev Microbiol. 2010; 8(4):251-9. DOI: 10.1038/nrmicro2312. View

5.
Suzuki M, Taylor L, Delong E . Quantitative analysis of small-subunit rRNA genes in mixed microbial populations via 5'-nuclease assays. Appl Environ Microbiol. 2000; 66(11):4605-14. PMC: 92356. DOI: 10.1128/AEM.66.11.4605-4614.2000. View