Literature DB >> 19709288

Prevalence of streptomycin-resistance genes in bacterial populations in European habitats.

Leo S van Overbeek1, Elisabeth M H Wellington, Sharon Egan, Kornelia Smalla, Holger Heuer, Jean-Marc Collard, Gillian Guillaume, Amalia D Karagouni, Theodora L Nikolakopoulou, Jan Dirk van Elsas.   

Abstract

The prevalence of selected streptomycin (Sm)-resistance genes, i.e. aph (3''), aph (6)-1d, aph (6)-1c, ant (3'') and ant (6), was assessed in a range of pristine as well as polluted European habitats. These habitats included bulk and rhizosphere soils, manure from farm animals, activated sludge from wastewater treatment plants and seawater. The methods employed included assessments of the prevalence of the genes in habitat-extracted DNA by PCR, followed by hybridisation with specific probes, Sm-resistant culturable bacteria and exogenous isolation of plasmids carrying Sm-resistance determinants. The direct DNA-based analysis showed that aph (6)-1d genes were most prevalent in the habitats examined. The presence of the other four Sm-modifying genes was demonstrated in 58% of the tested habitats. A small fraction of the bacterial isolates (8%) did not possess any of the selected Sm-modifying genes. These isolates were primarily obtained from activated sludge and manure. The presence of Sm-modifying genes in the isolates often coincided with the presence of IncP plasmids. Exogenous isolation demonstrated the presence of plasmids of 40-200 kb in size harbouring Sm-resistance genes from all the environments tested. Most plasmids were shown to carry the ant (3'') gene, often in combination with other Sm-resistance genes, such as aph (3'') and aph (6)-1d. The most commonly found Sm-modifying gene on mobile genetic elements was ant (3''). Multiple Sm-resistance genes on the same genetic elements appeared to be the rule rather than the exception. It is concluded that Sm-resistance genes are widespread in the environmental habitats studied and often occur on mobile genetic elements and ant (3'') was most often encountered.

Entities:  

Year:  2002        PMID: 19709288     DOI: 10.1111/j.1574-6941.2002.tb01018.x

Source DB:  PubMed          Journal:  FEMS Microbiol Ecol        ISSN: 0168-6496            Impact factor:   4.194


  20 in total

1.  Metagenomic analysis of apple orchard soil reveals antibiotic resistance genes encoding predicted bifunctional proteins.

Authors:  Justin J Donato; Luke A Moe; Brandon J Converse; Keith D Smart; Flora C Berklein; Patricia S McManus; Jo Handelsman
Journal:  Appl Environ Microbiol       Date:  2010-05-07       Impact factor: 4.792

2.  PCR detection of oxytetracycline resistance genes otr(A) and otr(B) in tetracycline-resistant streptomycete isolates from diverse habitats.

Authors:  Theodora L Nikolakopoulou; Sharon Egan; Leo S van Overbeek; Gilliane Guillaume; Holger Heuer; Elizabeth M H Wellington; Jan Dick van Elsas; Jean-Marc Collard; Kornelia Smalla; Amalia D Karagouni
Journal:  Curr Microbiol       Date:  2005-08-17       Impact factor: 2.188

3.  Tetracyclines and tetracycline resistance in agricultural soils: microcosm and field studies.

Authors:  Heike Schmitt; Krispin Stoob; Gerd Hamscher; Eric Smit; Willem Seinen
Journal:  Microb Ecol       Date:  2006-04-06       Impact factor: 4.552

4.  Prevalence of tetracycline resistance genes in Greek seawater habitats.

Authors:  Theodora L Nikolakopoulou; Eleni P Giannoutsou; Adamandia A Karabatsou; Amalia D Karagouni
Journal:  J Microbiol       Date:  2008-12-24       Impact factor: 3.422

5.  Influence of soil use on prevalence of tetracycline, streptomycin, and erythromycin resistance and associated resistance genes.

Authors:  Magdalena Popowska; Marzenna Rzeczycka; Antoni Miernik; Agata Krawczyk-Balska; Fiona Walsh; Brion Duffy
Journal:  Antimicrob Agents Chemother       Date:  2011-12-27       Impact factor: 5.191

6.  The evolution of no-cost resistance at sub-MIC concentrations of streptomycin in Streptomyces coelicolor.

Authors:  Sanne Westhoff; Tim Marijn van Leeuwe; Omar Qachach; Zheren Zhang; Gilles Philippus van Wezel; Daniel Eric Rozen
Journal:  ISME J       Date:  2017-01-17       Impact factor: 10.302

7.  Increased abundance and transferability of resistance genes after field application of manure from sulfadiazine-treated pigs.

Authors:  Sven Jechalke; Christoph Kopmann; Ingrid Rosendahl; Joost Groeneweg; Viola Weichelt; Ellen Krögerrecklenfort; Nikola Brandes; Mathias Nordwig; Guo-Chun Ding; Jan Siemens; Holger Heuer; Kornelia Smalla
Journal:  Appl Environ Microbiol       Date:  2013-01-11       Impact factor: 4.792

8.  Distribution of tetracycline and streptomycin resistance genes and class 1 integrons in Enterobacteriaceae isolated from dairy and nondairy farm soils.

Authors:  Velusamy Srinivasan; Hyang-Mi Nam; Ashish A Sawant; Susan I Headrick; Lien T Nguyen; Stephen P Oliver
Journal:  Microb Ecol       Date:  2007-08-15       Impact factor: 4.552

9.  Plant agricultural streptomycin formulations do not carry antibiotic resistance genes.

Authors:  Fabio Rezzonico; Virginia O Stockwell; Brion Duffy
Journal:  Antimicrob Agents Chemother       Date:  2009-05-04       Impact factor: 5.191

10.  Purification and characterization of aminoglycoside phosphotransferase APH(6)-Id, a streptomycin-inactivating enzyme.

Authors:  Meseret Ashenafi; Tatiana Ammosova; Sergei Nekhai; W Malcolm Byrnes
Journal:  Mol Cell Biochem       Date:  2013-11-19       Impact factor: 3.396

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