Grzegorz Nałęcz-Jawecki

Prof. Dr. Grzegorz Nałęcz-Jawecki

Department of Environmental Health Sciences, Medical University of Warsaw, Banacha 1, 02-097 Warszawa, Poland
+1
orcid

Research Focus & Metrics

Academic Career Length

34Years (1993-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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4 November 2003 in Environmental Toxicology
Verified
Journal Article
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GPGuido Persoone
Guido Persoone
BMBlahoslav Marsalek
Blahoslav Marsalek
IBIrina Blinova
Irina Blinova
ATAndrea Törökne
Andrea Törökne
DZDzidra Zarina
Dzidra Zarina
BKBoris Kolar
Boris Kolar

1 April 2005 in Chemosphere
Verified
Journal Article
Closed access
GPGrażyna Płaza
Grażyna Płaza
GNGrzegorz Nałęcz-Jawecki
Grzegorz Nałęcz-Jawecki
KUKrzysztof Ulfig
Krzysztof Ulfig
RBRobin L. Brigmon
Robin L. Brigmon

1 February 2011 in Chemosphere
Verified
Journal Article
Closed access
MMMarek Matejczyk
Marek Matejczyk
GPGrażyna Płaza
Grażyna Płaza
GNGrzegorz Nałęcz-Jawecki
Grzegorz Nałęcz-Jawecki
KUKrzysztof Ulfig
Krzysztof Ulfig
Agata Markowska-SzczupakAgata Markowska-Szczupak
Agata Markowska-Szczupak

4 June 2021 in PLOS ONE
Verified
Journal Article
Open access
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JHJakub Hubeny
Jakub Hubeny
MHMonika Harnisz
Monika Harnisz
Ewa KorzeniewskaEwa Korzeniewska
Ewa Korzeniewska
MBMartyna Buta
Martyna Buta
WZWiktor Zieliński
Wiktor Zieliński
GPGrażyna Płaza
Grażyna Płaza
The spread of antibiotic resistance is closely related with selective pressure in the environment. Wastewater from industrialized regions is characterized by higher concentrations of these pollutants than sewage from less industrialized areas. The aim of this study was to compare the concentrations of contaminants such as antibiotics and heavy metals (HMs), and to evaluate their impact on the spread of genes encoding resistance to antimicrobial drugs in samples of wastewater, sewage sludge and river water in two regions with different levels of industrialization. The factors exerting selective pressure, which significantly contributed to the occurrence of the examined antibiotic resistance genes (ARGs), were identified. The concentrations of selected gene copy numbers conferring resistance to four groups of antibiotics as well as class 1 and 2 integron-integrase genes were determined in the analyzed samples. The concentrations of six HMs and antibiotics corresponding to genes mediated resistance from 3 classes were determined. Based on network analysis, only some of the analyzed antibiotics correlated with ARGs, while HM levels were correlated with ARG concentrations, which can confirm the important role of HMs in promoting drug resistance. The samples from a wastewater treatment plant (WWTP) located an industrialized region were characterized by higher HM contamination and a higher number of significant correlations between the analyzed variables than the samples collected from a WWTP located in a less industrialized region. These results indicated that treated wastewater released into the natural environment can pose a continuous threat to human health by transferring ARGs, antibiotics and HMs to the environment. These findings shed light on the impact of industrialization on antibiotic resistance dissemination.

1 January 2003 in Ecotoxicology and Environmental Safety
Verified
Journal Article
Closed access
GNGrzegorz Nałęcz-Jawecki
Grzegorz Nałęcz-Jawecki
EGElżbieta Grabińska-Sota
Elżbieta Grabińska-Sota
PNPatrycja Narkiewicz
Patrycja Narkiewicz

24 March 2020 in Molecules
Verified
Journal Article
Open access
PDF file
JGJoanna Giebultowicz
Joanna Giebultowicz
GNGrzegorz Nałęcz-Jawecki
Grzegorz Nałęcz-Jawecki
MHMonika Harnisz
Monika Harnisz
DKDawid Kucharski
Dawid Kucharski
Ewa KorzeniewskaEwa Korzeniewska
Ewa Korzeniewska
GPGrażyna Płaza
Grażyna Płaza
In this study, a screening of 26 selected antimicrobials using liquid chromatography coupled to a tandem mass spectrometry method in two Polish wastewater treatment plants and their receiving surface waters was provided. The highest average concentrations of metronidazole (7400 ng/L), ciprofloxacin (4300 ng/L), vancomycin (3200 ng/L), and sulfamethoxazole (3000 ng/L) were observed in influent of WWTP2. Ciprofloxacin and sulfamethoxazole were the most dominant antimicrobials in influent and effluent of both WWTPs. In the sludge samples the highest mean concentrations were found for ciprofloxacin (up to 28 μg/g) and norfloxacin (up to 5.3 μg/g). The removal efficiency of tested antimicrobials was found to be more than 50% for both WWTPs. However, the presence of antimicrobials influenced their concentrations in the receiving waters. The highest antimicrobial resistance risk was estimated in influent of WWTPs for azithromycin, ciprofloxacin, clarithromycin, metronidazole, and trimethoprim and in the sludge samples for the following antimicrobials: azithromycin, ciprofloxacin, clarithromycin, norfloxacin, trimethoprim, ofloxacin, and tetracycline. The high environmental risk for exposure to azithromycin, clarithromycin, and sulfamethoxazole to both cyanobacteria and eukaryotic species in effluents and/or receiving water was noted. Following the obtained results, we suggest extending the watch list of the Water Framework Directive for Union-wide monitoring with sulfamethoxazole.