scholarly journals Distribution Characteristics of Antibiotic Resistance Bacteria and Related Genes in Urban Recreational Lakes Replenished by Different Supplementary Water Source

Author(s):  
Yongqiang Li ◽  
Chong-Miao Zhang ◽  
Xiao Mou ◽  
Peipei Zhang ◽  
Jie Liang ◽  
...  

Abstract The objective of this study was to investigate the distribution characteristics of antibiotic resistant bacteria (ARB) and antibiotic resistance genes (ARGs) in urban recreational water with different water supply sources, 2 lakes as XQ and FQ which represented as surface water and reclaimed water were selected for the study. Water samples were collected from April to November in 2018 to investigate aspects including 8 physical and chemical indexes of waters, resistance degree of 5 different kinds of antibiotics, antimicrobial resistance heterotrophic bacteria content, resistance phenotype, antibiotic resistance gene types and antibiotic resistance strains of species distribution. The results showed that the changes of antibiotic resistance rate of heterotrophic bacteria in 2 lakes to 5 kinds of antibiotics were synchronous with time, and it would reach its maximum in autumn. The detection of 10 ARGs and intⅠ gene in 80 strains screened out from 125 strains of heterotrophic bacteria showed that the detection rate of tetG and tetA genes was relatively high, especially intI, with the rate as high as 90%. In the detection of resistance spectrum, 51.25% of the resistance bacteria were double-resistance to AMP-CTX. The 80 isolate strains were of 9 genera and 19 species, among which Bacillus cereus, Escherichia coli, Aeromonas veronii, Aeromonas caviae and Raoultella ornithinolytica were the common ARB species in FQ and XQ. There was no relatively large differences in the content of ARB, detection rate, and identification of ARGs in 2 lakes. Correlation analysis was used to evaluate the association between the change of water quality indexes and the content of antibiotic resistance bacteria in 2 lakes, and it was found that the water temperature was significantly correlated with the content of ARB in Sulfamethoxazole and Cefotaxime (p<0.05), while there were no other correlations between the changes of other water quality indexes and the content of ARB (p>0.05).

2021 ◽  
Author(s):  
Yi Wu ◽  
Xun Zhang ◽  
Baiyu Wang ◽  
Ying Wang ◽  
Yuzhu Gao ◽  
...  

Abstract To understand the distribution characteristics of antibiotic resistance genes (ARGs) and mobile genetic elements (MGEs) in vegetable soil in the main facility agriculture distribution centres of Liaoning Province, 13 soil samples from seven sites including Chaoyang Yandu Xincheng, Zhuanghe, and Fushun were collected to detect the species and abundance of ARGs and MGEs, and analyse their correlation. The results showed that the ARGs were mainly tetracycline and macrolide antibiotic resistance genes, the transportable elements were transposases, and the cell protection and cell discharge pump was the main resistance mechanism. The detection rate of tetm-02, oprj, sul2, blaTEM, fox5, ermX, ermB, and ermF was 100%. The detection rate of integron IntΙ-1 and transposable enzyme tnpA-01 was 100%. The highest content of antibiotic resistance genes was found in Qiandangpu Village, Daying Town, and Zhuanghe City, followed by Wutun Village, Miaojia Village, Daying Town, and Dalian. Correlation analysis showed a correlation between the abundance of ARGs and the abundance of MGEs in agricultural soil. There was a significant positive correlation between the abundance of ARGs and integron (P < 0.05). The results of this study provide data support for the assessment of soil ARG pollution levels and the effective prevention and control of ARG transmission risk in the main protected vegetable fields in Liaoning Province.


2018 ◽  
Vol 19 (1) ◽  
pp. 179-190
Author(s):  
R. Destiani ◽  
M. R. Templeton

Abstract This study assessed the occurrence and prevalence of antibiotic-resistant bacteria (ARBs) and antibiotic resistance genes (ARGs) in tap water sampled across London, United Kingdom. Sampling was conducted seasonally from nine locations spread geographically across the city. ARBs and ARGs (tet(A), dfrA7, and sul1) were detected in all sampling locations in all sampling rounds. Resistance to trimethoprim was the highest among the tested antibiotics and the sul1 gene was the most abundant resistance gene detected. Several opportunistic pathogens were identified amongst the ARBs in the water samples, including Pseudomonas aeruginosa and Stenotrophomonas maltophilia.


2021 ◽  
Author(s):  
Johan Bengtsson-Palme ◽  
Viktor Jonsson ◽  
Stefanie Heß

AbstractIt is generally accepted that intervention strategies to curb antibiotic resistance cannot solely focus on human and veterinary medicine but must also consider environmental settings. While the environment clearly has a role in the transmission of resistant bacteria, it is less clear what role it plays in the emergence of novel types of resistance. It has been suggested that the environment constitutes an enormous recruitment ground for resistance genes to pathogens, but the extent to which this actually happens is unknown. In this study, we built a model framework for resistance emergence and used the available quantitative data on the relevant processes to identify the steps which are limiting the appearance of antibiotic resistance determinants in human or animal pathogens. We also assessed the effect of uncertainty in the available data on the model results. We found that in a majority of scenarios, the environment would only play a minor role in the emergence of novel resistance genes. However, the uncertainty around this role is enormous, highlighting an urgent need of more quantitative data to understand the role of the environment in antibiotic resistance development. Specifically, more data is most needed on the fitness costs of antibiotic resistance gene (ARG) carriage, the degree of dispersal of resistant bacteria from the environment to humans, but also the rates of mobilization and horizontal transfer of ARGs. Quantitative data on these processes is instrumental to determine which processes that should be targeted for interventions to curb development and transmission of resistance.


2016 ◽  
Vol 62 (2) ◽  
pp. 353-359 ◽  
Author(s):  
G Terrance Walker ◽  
Tony J Rockweiler ◽  
Rossio K Kersey ◽  
Kelly L Frye ◽  
Susan R Mitchner ◽  
...  

Abstract BACKGROUND Multiantibiotic-resistant bacteria pose a threat to patients and place an economic burden on health care systems. Carbapenem-resistant bacilli and extended-spectrum β-lactamase (ESBL) producers drive the need to screen infected and colonized patients for patient management and infection control. METHODS We describe a multiplex microfluidic PCR test for perianal swab samples (Acuitas® MDRO Gene Test, OpGen) that detects the vancomycin-resistance gene vanA plus hundreds of gene subtypes from the carbapenemase and ESBL families Klebsiella pneumoniae carbapenemase (KPC), New Delhi metallo-β-lactamase (NDM), Verona integron-mediated metallo-β-lactamase (VIM), imipenemase metallo-β-lactamase (IMP), OXA-23, OXA-48, OXA-51, CTX-M-1, and CTX-M-2, regardless of the bacterial species harboring the antibiotic resistance. RESULTS Analytical test sensitivity per perianal swab is 11–250 CFU of bacteria harboring the antibiotic resistance genes. Test throughput is 182 samples per test run (1820 antibiotic resistance gene family results). We demonstrate reproducible test performance and 100% gene specificity for 265 clinical bacterial organisms harboring a variety of antibiotic resistance genes. CONCLUSIONS The Acuitas MDRO Gene Test is a sensitive, specific, and high-throughput test to screen colonized patients and diagnose infections for several antibiotic resistance genes directly from perianal swab samples, regardless of the bacterial species harboring the resistance genes.


2014 ◽  
Vol 2014 ◽  
pp. 1-10 ◽  
Author(s):  
Ana Belén Flórez ◽  
Ángel Alegría ◽  
Franca Rossi ◽  
Susana Delgado ◽  
Giovanna E. Felis ◽  
...  

Large antibiotic resistance gene pools in the microbiota of foods may ultimately pose a risk for human health. This study reports the identification and quantification of tetracycline- and erythromycin-resistant populations, resistance genes, and gene diversity in traditional Spanish and Italian cheeses, via culturing, conventional PCR, real-time quantitative PCR (qPCR), and denaturing gradient gel electrophoresis (DGGE). The numbers of resistant bacteria varied widely among the antibiotics and the different cheese varieties; in some cheeses, all the bacterial populations seemed to be resistant. Up to eight antibiotic resistance genes were sought by gene-specific PCR, six with respect to tetracycline, that is,tet(K),tet(L),tet(M),tet(O),tet(S), andtet(W), and two with respect to erythromycin, that is,erm(B) anderm(F). The most common resistance genes in the analysed cheeses weretet(S),tet(W),tet(M), anderm(B). The copy numbers of these genes, as quantified by qPCR, ranged widely between cheeses (from 4.94 to10.18log⁡10/g). DGGE analysis revealed distinct banding profiles and two polymorphic nucleotide positions fortet(W)-carrying cheeses, though the similarity of the sequences suggests thistet(W) to have a monophyletic origin. Traditional cheeses would therefore appear to act as reservoirs for large numbers of many types of antibiotic resistance determinants.


Author(s):  
Célia P. F. Domingues ◽  
João S. Rebelo ◽  
Teresa Nogueira ◽  
Joël Pothier ◽  
Francisca Monteiro ◽  
...  

1.AbstractThis study aims to understand the cause of the recent observation that humans with a higher diversity of virulence genes in their metagenomes tend to be precisely those with higher diversity of antibiotic-resistance genes. We simulated the transferring of virulence and antibiotic-resistance genes in a community of interacting people where some take antibiotics. The diversities of the two genes types became positively correlated whenever the contagion probability between two people was higher than the probability of losing resistant genes. However, no such positive correlations arise if no one takes antibiotics. This finding holds even under changes of several simulations’ parameters, such as the relative or total diversity of virulence and resistance genes, the contagion probability between individuals, the loss rate of resistance genes, or the social network type. Because the loss rate of resistance genes may be shallow, we conclude that the contagion between people and antibiotic usage is the leading cause of establishing the positive correlation mentioned above. Therefore, antibiotic use and something as prosaic as the contagion between people may facilitate the emergence of virulent and multi-resistant bacteria in people’s metagenomes with a high diversity of both gene types. These superbugs may then circulate in the community.


mBio ◽  
2014 ◽  
Vol 5 (5) ◽  
Author(s):  
Christopher J. Harmer ◽  
Robert A. Moran ◽  
Ruth M. Hall

ABSTRACTThe insertion sequence IS26plays a key role in disseminating antibiotic resistance genes in Gram-negative bacteria, forming regions containing more than one antibiotic resistance gene that are flanked by and interspersed with copies of IS26. A model presented for a second mode of IS26movement that explains the structure of these regions involves a translocatable unit consisting of a unique DNA segment carrying an antibiotic resistance (or other) gene and a single IS copy. Structures resembling class I transposons are generated via RecA-independent incorporation of a translocatable unit next to a second IS26such that the ISs are in direct orientation. Repeating this process would lead to arrays of resistance genes with directly oriented copies of IS26at each end and between each unique segment. This model requires that IS26recognizes another IS26as a target, and in transposition experiments, the frequency of cointegrate formation was 60-fold higher when the target plasmid contained IS26. This reaction was conservative, with no additional IS26or target site duplication generated, and orientation specific as the IS26s in the cointegrates were always in the same orientation. Consequently, the cointegrates were identical to those formed via the known mode of IS26movement when a target IS26was not present. Intact transposase genes in both IS26s were required for high-frequency cointegrate formation as inactivation of either one reduced the frequency 30-fold. However, the IS26target specificity was retained. Conversion of each residue in the DDE motif of the Tnp26 transposase also reduced the cointegration frequency.IMPORTANCEResistance to antibiotics belonging to several of the different classes used to treat infections is a critical problem. Multiply antibiotic-resistant bacteria usually carry large regions containing several antibiotic resistance genes, and in Gram-negative bacteria, IS26is often seen in these clusters. A model to explain the unusual structure of regions containing multiple IS26copies, each associated with a resistance gene, was not available, and the mechanism of their formation was unexplored. IS26-flanked structures deceptively resemble class I transposons, but this work reveals that the features of IS26movement do not resemble those of the IS and class I transposons studied to date. IS26uses a novel movement mechanism that defines a new family of mobile genetic elements that we have called “translocatable units.” The IS26mechanism also explains the properties of IS257(IS431) and IS1216, which belong to the same IS family and mobilize resistance genes in Gram-positive staphylococci and enterococci.


2018 ◽  
Author(s):  
Vanessa R. Marcelino ◽  
Michelle Wille ◽  
Aeron C. Hurt ◽  
Daniel González-Acuña ◽  
Marcel Klaassen ◽  
...  

AbstractAntibiotic resistance is rendering common bacterial infections untreatable. Wildlife can incorporate and disperse antibiotic resistant bacteria in the environment, such as water systems, which in turn serve as reservoirs of resistance genes for human pathogens. We used bulk RNA-sequencing (meta-transcriptomics) to assess the diversity and expression levels of functionally active resistance genes in the microbiome of birds with aquatic behavior. We sampled birds across a range of habitats, from penguins in Antarctica to ducks in a wastewater treatment plant in Australia. This revealed 81 antibiotic resistance genes in birds from all localities, including β-lactam, tetracycline and chloramphenicol resistance in Antarctica, and genes typically associated with multidrug resistance plasmids in areas with high human impact. Notably, birds feeding at a wastewater treatment plant carried the greatest resistance gene burden, suggesting that human waste, even if it undergoes treatment, contributes to the spread of antibiotic resistance genes to the wild. Differences in resistance gene burden also reflected the birds’ ecology, taxonomic group and microbial functioning. Ducks, which feed by dabbling, carried a higher abundance and diversity of resistance genes than turnstones, avocets and penguins, that usually prey on more pristine waters. In sum, this study helps to reveal the complex factors explaining the distribution of resistance genes and their exchange routes between humans and wildlife.


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