The
occurrence and distribution of 20 subtypes of antibiotic resistance
genes (ARGs), conferring sulfonamide, tetracycline, macrolide, β-lactam,
aminoglycoside, or quinolone antibiotic resistance, were investigated
in urban dust samples collected from the surfaces of three megacities
(Beijing, Tianjin, and Shijiazhuang) of northern China. Real-time
polymerase chain reaction indicated that the abundance of ARGs and
16S rRNA genes was significantly higher in the summer than in the
winter. A total of 80 antibiotic-resistant bacteria were isolated
and identified, and 12 of those species were identified as opportunistic
pathogens. An isolated pathogen Acinetobacter sp.
was proven to be able to transfer antibiotic resistance, which highlights
the potential risk that an urban dust-associated ARG poses to public
health. Deep 16S rRNA sequencing indicated high heterogeneity of bacterial
communities among cities in the summer, but great homogeneity in the
winter. In the summer, Enterococcus, Massilia, and Anthrobacter were the most prevalent genera
in Tianjin, Beijing, and Shijiazhuang, respectively. However, the
most prevalent bacterial genera were Bacillus and Lactococcus in the winter. This is the first study of the
occurrence and distribution of the urban dust-associated bacterial
community and its associated bacterial antibiotic resistance in northern
China. This study highlights the risk of dust-associated antibiotic
resistance to public health.
The emergence and spread of NDM-1
(New Delhi metallo-β-lactamase-1)
are of great concern to public health. Our previous study reported
the occurrence and persistence of NDM-1 genes in wastewater treatment
plants (WWTPs). In this study, the occurrence and fate of NDM-1 genes
and host bacteria were investigated in a WWTP discharge-receiving
river. A considerable level of NDM-1 genes occurred in the receiving
river, whereas no NDM-1 genes were detected upstream of the WWTP.
This finding together with the DNA sequencing of NDM-1 genes demonstrated
that the river NDM-1 is derived from the WWTP. Opportunistic pathogens,
like Shigella sonnei, Enterococcus faecium, and Wautersiella falsenii, were isolated from
both the receiving water and the WWTP. This study underscores the
need to mitigate the release of NDM-1 from WWTPs and indicates that
more attention should to be paid to the propagation of these genes
to the receiving environment to alleviate their worldwide dissemination.
An expanding list of chemicals may permeabilize bacterial cells and facilitate horizontal gene transfer (HGT), which enhances propagation of antibiotic resistance genes (ARGs) in the environment. Previous studies showed that 1-butyl-3-methylimidazolium hexafluorophosphate ([BMIm][PF6]), an ionic liquid, can facilitate HGT of some ARGs among bacteria. However, the dynamic response of a wider range of ARGs and associated mobile genetic elements (MGEs) in different environments is unknown. Here, we used metagenomic tools to study shifts of the resistome and microbiome in both sediments and freshwater microcosms exposed to [BMIm][PF6]. Exposure for 16 h to 0.1 or 1.0 g/L significantly enriched more than 207 ARG subtypes primarily encoding efflux pumps in freshwater microcosms as well as cultivable antibioticresistant bacteria. This resistome enrichment was attributed to HGT facilitated by MGEs (428 plasmids, 61 integron-integrase genes, and 45 gene cassettes were enriched) as well as to HGT-related functional genes. Interestingly, resistome enrichment occurred fast (within 16 h) after [BMIm][PF6] exposure, before any significant changes in bacterial community structure. Similar ARG enrichment occurred in sediment microcosms exposed to [BMIm][PF6] for 28 d, and this longer exposure affected the microbial community structure (e.g., Proteobacteria abundance increased significantly). Overall, this study suggests that [BMIm][PF6] releases could rapidly enrich the antibiotic resistome in receiving environments by increasing HGT and fortuitously selecting for efflux pump genes, thus contributing to ARG propagation.
Wild birds are known to harbor and
discharge antibiotic-resistant
bacteria (ARB) and their associated antibiotic resistance genes (ARGs).
However, assessments of their contribution to the dissemination of
antibiotic resistance in the environment are limited to culture-dependent
bacterial snapshots. Here, we present a high-throughput sequencing
study that corroborates extensive ARG exchange between wild bird feces
and their habitats and implies the need to scrutinize high-mobility
birds as potential vectors for global propagation of ARGs. We characterized
the resistome (281 ARGs) and microbiome of seven wild bird species
and their terrestrial and aquatic habitats. The resistomes of bird
feces were influenced by the microbial community structure, mobile
genetic elements (MGEs), and residual antibiotics. We designated 33
ARGs found in more than 90% of the bird fecal samples as core ARGs
of wild bird feces, among which 16 ARGs were shared as core ARGs in
both wild bird feces and their habitats; these genes represent a large
proportion of both the bird feces (35.0 ± 15.9%) and the environmental
resistome (29.9 ± 21.4%). One of the most detected β-lactam
resistance genes (bla
TEM, commonly harbored
by multidrug resistant “superbugs”) was used as molecular
marker to demonstrate the high interconnectivity of ARGs between the
microbiomes of wild birds and their habitats. Overall, this work provides
a comprehensive analysis of the wild bird resistome and underscores
the importance to consider genetic exchange between animals and the
environment in the One Health approach.
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