Free ammonia pretreatment enhances the removal of antibiotic resistance genes in anaerobic sludge digestion

Chemosphere ◽  
2021 ◽  
pp. 130910
Author(s):  
Zehao Zhang ◽  
Xuan Li ◽  
Huan Liu ◽  
Li Gao ◽  
Qilin Wang
2020 ◽  
Author(s):  
Zehao Zhang ◽  
Huan Liu ◽  
Qilin Wang

AbstractSludge from the wastewater treatment plants (WWTPs) has been recognized as a reservoir of antibiotic resistance genes (ARGs). Free ammonia (FA, i.e. NH3-N) pretreatment has been demonstrated to be able to enhance anaerobic digestion, which is a widely used method for sludge treatment. However, the effect of combined FA pretreatment and anaerobic digestion on the fate of ARGs is still unknown. This study demonstrated for the first time that combined FA pretreatment (420 mg NH3-N/L for 24 h) and anaerobic digestion could reduce the abundances of the tested ARGs by 0.06 log10 gene copies/g TS (total solids) compared with the anaerobic digestion alone. Specifically, the experimental results showed that combined FA pretreatment and anaerobic digestion reduced the abundances of aac(6’)-Ib-cr, blaTEM, sul2, tetA, tetB and tetX by 0.07, 0.37, 0.09, 0.32, 0.24 and 0.59 log10 gene copies/g TS compared with anaerobic digestion alone. In contrast, combined FA pretreatment and anaerobic digestion slightly increased the abundance of tetG by 0.05 log10 gene copies/g TS compared with anaerobic digestion alone. In addition, FA pretreatment did not significantly affect the abundance of sul1 and tetM during anaerobic digestion. This study revealed that FA pretreatment for anaerobic digestion could potentially reduce the spread of antibiotic resistance from the sludge to soil (while agriculture reuse is used as the sludge disposal method), thereby protecting the environment and human health.


2016 ◽  
Vol 1 (2) ◽  
pp. 22 ◽  
Author(s):  
Navindra Kumari Palanisamy ◽  
Parasakthi Navaratnam ◽  
Shamala Devi Sekaran

Introduction: Streptococcus pneumoniae is an important bacterial pathogen, causing respiratory infection. Penicillin resistance in S. pneumoniae is associated with alterations in the penicillin binding proteins, while resistance to macrolides is conferred either by the modification of the ribosomal target site or efflux mechanism. This study aimed to characterize S. pneumoniae and its antibiotic resistance genes using 2 sets of multiplex PCRs. Methods: A quintuplex and triplex PCR was used to characterize the pbp1A, ermB, gyrA, ply, and the mefE genes. Fifty-eight penicillin sensitive strains (PSSP), 36 penicillin intermediate strains (PISP) and 26 penicillin resistance strains (PRSP) were used. Results: Alteration in pbp1A was only observed in PISP and PRSP strains, while PCR amplification of the ermB or mefE was observed only in strains with reduced susceptibility to erythromycin. The assay was found to be sensitive as simulated blood cultures showed the lowest level of detection to be 10cfu. Conclusions: As predicted, the assay was able to differentiate penicillin susceptible from the non-susceptible strains based on the detection of the pbp1A gene, which correlated with the MIC value of the strains.


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