2022
DOI: 10.1016/j.ijmm.2022.151559
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Comprehensive investigation of antibiotic resistance gene content in cfiA-harboring Bacteroides fragilis isolates of human and animal origins by whole genome sequencing

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Cited by 14 publications
(9 citation statements)
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“…This plasmid was also detected in 4/5 MDR B. fragilis isolates from the Netherlands and 2/23 cfiA -harbouring B. fragilis isolates from Hong Kong. 12 , 21 The P. melaninogenica isolate resistant to metronidazole harboured a nimA gene in its chromosome. The nimA gene can be present on plasmids and in the chromosome.…”
Section: Discussionmentioning
confidence: 99%
“…This plasmid was also detected in 4/5 MDR B. fragilis isolates from the Netherlands and 2/23 cfiA -harbouring B. fragilis isolates from Hong Kong. 12 , 21 The P. melaninogenica isolate resistant to metronidazole harboured a nimA gene in its chromosome. The nimA gene can be present on plasmids and in the chromosome.…”
Section: Discussionmentioning
confidence: 99%
“…Genomic DNA of each strain was extracted and qualified as was done in our previous studies [ 19 , 20 ]. All genomes were sequenced using the Illumina NovaSeq platform (Illumina, CA, USA) at the Novogene Bioinformatics Institute, Beijing.…”
Section: Methodsmentioning
confidence: 99%
“…All genomes were sequenced using the Illumina NovaSeq platform (Illumina, CA, USA) at the Novogene Bioinformatics Institute, Beijing. The workflow from raw reads to generate annotated genomes employed in our previous studies was performed [ 19 , 20 ]. Databases of CTX-M and CTX-M-like protein sequences were curated after comprehensively screening all available databases including the updated Bacterial Antimicrobial Resistance Reference Gene Database ( , accessed on 1 November 2022), BLDB ( , accessed on 1 November 2022), ResFinder (upon the date of September 2022) and HMD-ARG-DB [ 21 ].…”
Section: Methodsmentioning
confidence: 99%
“…The Illumina short reads were then trimmed with Trimmomatic v0.39 and the Nanopore long reads were trimmed by Porechop version 0.2.4. The trimmed reads proceeded to de novo assembly using Unicycler v0.4.9, as in our previous studies [ 25 , 26 ]. In the case of an incomplete genome generated from Unicycler, CANU v2.2 [ 27 ] or Flye v2.9.1 [ 28 ] was used to assemble the Nanopore reads and corrected with Pilon v1.24 [ 29 ].…”
Section: Methodsmentioning
confidence: 99%
“…In the case of an incomplete genome generated from Unicycler, CANU v2.2 [ 27 ] or Flye v2.9.1 [ 28 ] was used to assemble the Nanopore reads and corrected with Pilon v1.24 [ 29 ]. Quality evaluations, fixations of the start position with dnaA , and annotations of genomes were performed as described in our previous studies [ 25 , 26 ].…”
Section: Methodsmentioning
confidence: 99%