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Antibiotic resistance genes and class 1 integron: Evidence of fecal pollution as a major driver for their abundance in water and sediments impacted by metal contamination and wastewater in the Andean region of Bolivia

https://doi.org/10.1101/2020.03.23.003350

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/bf00766705openalex-snapshot

Field assessment of acid mine drainage contamination in surface and ground water

inferredcites →https://doi.org/10.1007/bf02186967openalex-snapshot

The pH regime of sediments underlying acidified waters

inferredcites →https://doi.org/10.1007/s00253-015-6404-9openalex-snapshot

Impacts of coexisting antibiotics, antibacterial residues, and heavy metals on the occurrence of erythromycin resistance genes in urban wastewater

inferredcites →https://doi.org/10.1007/s00253-015-6416-5openalex-snapshot

Increased levels of antibiotic resistance in urban stream of Jiulongjiang River, China

inferredcites →https://doi.org/10.1007/s11783-014-0679-4openalex-snapshot

Modified pretreatment method for total microbial DNA extraction from contaminated river sediment

inferredcites →https://doi.org/10.1016/j.agrformet.2019.107710openalex-snapshot

Unraveling the impacts of droughts and agricultural intensification on the Altiplano water resources

inferredcites →https://doi.org/10.1016/j.apgeochem.2007.11.019openalex-snapshot

Contamination of surface waters by mining wastes in the Milluni Valley (Cordillera Real, Bolivia): Mineralogical and hydrological influences

inferredcites →https://doi.org/10.1016/j.chemosphere.2018.12.041openalex-snapshot

The mobility of thallium in sediments and source apportionment by lead isotopes

inferredcites →https://doi.org/10.1016/j.copbio.2008.05.006openalex-snapshot

Antibiotics and antibiotic resistance in water environments

inferredcites →https://doi.org/10.1016/j.cub.2014.03.036openalex-snapshot

Large-Scale Metagenomic-Based Study of Antibiotic Resistance in the Environment

inferredcites →https://doi.org/10.1016/j.envpol.2016.10.075openalex-snapshot

Nutrients, heavy metals and microbial communities co-driven distribution of antibiotic resistance genes in adjacent environment of mariculture

inferredcites →https://doi.org/10.1016/j.envpol.2017.08.009openalex-snapshot

Mercury contamination level and speciation inventory in Lakes Titicaca & Uru-Uru (Bolivia): Current status and future trends

inferredcites →https://doi.org/10.1016/j.gexplo.2007.04.011openalex-snapshot

Abandoned mine sites as a source of contamination by heavy metals: A case study in a semi-arid zone

inferredcites →https://doi.org/10.1016/j.scitotenv.2010.05.015openalex-snapshot

Environmental impact of mining activities on the surface water quality in Tibet: Gyama valley

inferredcites →https://doi.org/10.1016/j.scitotenv.2012.03.054openalex-snapshot

Evaluation of quantitative real-time PCR workflow modifications on 16S rRNA and tetA gene quantification in environmental samples

inferredcites →https://doi.org/10.1016/j.scitotenv.2016.10.129openalex-snapshot

Antibiotic pollution in the Katari subcatchment of the Titicaca Lake: Major transformation products and occurrence of resistance genes

inferredcites →https://doi.org/10.1016/j.scitotenv.2017.10.312openalex-snapshot

Antibiotics and common antibacterial biocides stimulate horizontal transfer of resistance at low concentrations

inferredcites →https://doi.org/10.1016/j.scitotenv.2018.11.372openalex-snapshot

Evidence for co-selection of antibiotic resistance genes and mobile genetic elements in metal polluted urban soils

inferredcites →https://doi.org/10.1016/j.tim.2006.02.006openalex-snapshot

Co-selection of antibiotic and metal resistance

inferredcites →https://doi.org/10.1016/j.tim.2013.11.001openalex-snapshot

The role of aquatic ecosystems as reservoirs of antibiotic resistance

inferredcites →https://doi.org/10.1016/j.tim.2018.08.003openalex-snapshot

Pollutants That Replicate: Xenogenetic DNAs

inferredcites →https://doi.org/10.1016/j.tree.2011.03.004openalex-snapshot

Aquatic systems: maintaining, mixing and mobilising antimicrobial resistance?

inferredcites →https://doi.org/10.1016/j.watres.2019.115098openalex-snapshot

Source identification of antibiotic resistance genes in a peri-urban river using novel crAssphage marker genes and metagenomic signatures

inferredcites →https://doi.org/10.1021/acs.est.6b05342openalex-snapshot

Comparison of Metals and Tetracycline as Selective Agents for Development of Tetracycline Resistant Bacterial Communities in Agricultural Soil

inferredcites →https://doi.org/10.1021/acs.est.8b00638openalex-snapshot

Correlation of crAssphage qPCR Markers with Culturable and Molecular Indicators of Human Fecal Pollution in an Impacted Urban Watershed

inferredcites →https://doi.org/10.1021/acs.estlett.9b00130openalex-snapshot

Co-Occurrence of crAssphage with Antibiotic Resistance Genes in an Impacted Urban Watershed

inferredcites →https://doi.org/10.1021/es101657sopenalex-snapshot

Tracking Antibiotic Resistance Genes in the South Platte River Basin Using Molecular Signatures of Urban, Agricultural, And Pristine Sources

inferredcites →https://doi.org/10.1038/ismej.2014.226openalex-snapshot

Using the class 1 integron-integrase gene as a proxy for anthropogenic pollution

inferredcites →https://doi.org/10.1038/nature13377openalex-snapshot

Bacterial phylogeny structures soil resistomes across habitats

inferredcites →https://doi.org/10.1038/ncomms5498openalex-snapshot

A highly abundant bacteriophage discovered in the unknown sequences of human faecal metagenomes

inferredcites →https://doi.org/10.1038/nmicrobiol.2016.270openalex-snapshot

Continental-scale pollution of estuaries with antibiotic resistance genes

inferredcites →https://doi.org/10.1038/nrmicro3439openalex-snapshot

Tackling antibiotic resistance: the environmental framework

inferredcites →https://doi.org/10.1038/s41467-018-07992-3openalex-snapshot

Fecal pollution can explain antibiotic resistance gene abundances in anthropogenically impacted environments

inferredcites →https://doi.org/10.1038/s41586-018-0386-6openalex-snapshot

Structure and function of the global topsoil microbiome

inferredcites →https://doi.org/10.1038/s41598-017-05260-wopenalex-snapshot

Soil bacterial quantification approaches coupling with relative abundances reflecting the changes of taxa

inferredcites →https://doi.org/10.1039/c6em00547kopenalex-snapshot

Synergistic effects of mining and urban effluents on the level and distribution of methylmercury in a shallow aquatic ecosystem of the Bolivian Altiplano

inferredcites →https://doi.org/10.1073/pnas.1222743110openalex-snapshot

Diverse and abundant antibiotic resistance genes in Chinese swine farms

inferredcites →https://doi.org/10.1093/nar/gkz935openalex-snapshot

CARD 2020: antibiotic resistome surveillance with the comprehensive antibiotic resistance database

inferredcites →https://doi.org/10.1111/1751-7915.12841openalex-snapshot

Determination of crAssphage in water samples and applicability for tracking human faecal pollution

inferredcites →https://doi.org/10.1111/j.1462-2920.2006.01091.xopenalex-snapshot

Coselection for microbial resistance to metals and antibiotics in freshwater microcosms

inferredcites →https://doi.org/10.1128/aem.00335-09openalex-snapshot

Pyrosequencing-Based Assessment of Soil pH as a Predictor of Soil Bacterial Community Structure at the Continental Scale

inferredcites →https://doi.org/10.1128/aem.02168-17openalex-snapshot

Metagenomics Reveals the Impact of Wastewater Treatment Plants on the Dispersal of Microorganisms and Genes in Aquatic Sediments

inferredcites →https://doi.org/10.1177/2042098614554919openalex-snapshot

Antimicrobial resistance: risk associated with antibiotic overuse and initiatives to reduce the problem

inferredcites →https://doi.org/10.1186/1471-2105-13-134openalex-snapshot

Primer-BLAST: A tool to design target-specific primers for polymerase chain reaction

inferredcites →https://doi.org/10.1186/s40064-016-2132-6openalex-snapshot

Impact of urban contamination of the La Paz River basin on thermotolerant coliform density and occurrence of multiple antibiotic resistant enteric pathogens in river water, irrigated soil and fresh vegetables

inferredcites →https://doi.org/10.1186/s40168-018-0424-5openalex-snapshot

A reservoir of ‘historical’ antibiotic resistance genes in remote pristine Antarctic soils

inferredcites →https://doi.org/10.1371/journal.pone.0210735openalex-snapshot

Diarrheal bacterial pathogens and multi-resistant enterobacteria in the Choqueyapu River in La Paz, Bolivia

inferredcites →https://doi.org/10.1371/journal.pone.0218277openalex-snapshot

Strong correlation of total phenotypic resistance of samples from household environments and the prevalence of class 1 integrons suggests for the use of the relative prevalence of intI1 as a screening tool for multi-resistance

inferredcites →https://doi.org/10.3389/fmicb.2018.00852openalex-snapshot

Human Activity Determines the Presence of Integron-Associated and Antibiotic Resistance Genes in Southwestern British Columbia

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1099/jmm.0.001704openalex-snapshot

Class 1 integrons in clinical and swine industry isolates of Salmonella Typhimurium from Colombia, dating 1997 to 2017

inferred← citeshttps://doi.org/10.3390/w13162234openalex-snapshot

Prevalence of Antibiotic Resistance Genes in the Saigon River Impacted by Anthropogenic Activities

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