Back to Search Start Over

Whole-Genome Sequencing of a Multidrug-Resistant Strain: Delftia acidovorans B408.

Authors :
Li K
Liu X
Zuo W
Wu N
Source :
Biochemical genetics [Biochem Genet] 2023 Jun; Vol. 61 (3), pp. 1086-1096. Date of Electronic Publication: 2022 Nov 30.
Publication Year :
2023

Abstract

Background: Delftia acidovorans is distributed widely in the environment and has the potential to promote the growth of plants and degrade organic pollutants. However, it is also an opportunistic pathogen for human and many reports demonstrated that D. acidovorans has strong resistance to aminoglycosides and polymyxins.<br />Objective: The aim of this work was to reveal the antibiotic resistance genes and pathogenic genes in a novel conditional pathogenic strain-D. acidovorans B804, which was isolated from the radiation-polluted soil from Xinjiang Uyghur Autonomous Region, China.<br />Methods: The antibiotic resistance test was performed according to the Kirby-Bauer disk diffusion method and evaluated by the standards of the Clinical and Laboratory Standards Institute guidelines. The genome of D. acidovorans B804 was sequenced by a PacBio RS II and Illumina HiSeq 4000 platform in Shanghai Majorbio Biopharm Technology Co., Ltd. (Shanghai, China).<br />Results: The multidrug resistance phenotypes of D. acidovorans B804 was experimentally confirmed and its genome was sequenced. The total size of D. acidovorans B804 genome was 6,661,314 bp with a GC content of 66.73%. 403 genes associated with antibiotic resistances were predicted. Meanwhile, 89 pathogenic genes were also predicted and 17 of these genes might be capable of causing diseases to human, such as infections and salmonellosis.<br />Conclusions: This genomic information can be used as a reference sequence for comparative genomic studies. The results provided more insights regarding the pathogenesis and drug resistance mechanism of D. acidovorans, which will be meaningful for developing more effective therapies toward D. acidovorans-related diseases.<br /> (© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.)

Details

Language :
English
ISSN :
1573-4927
Volume :
61
Issue :
3
Database :
MEDLINE
Journal :
Biochemical genetics
Publication Type :
Academic Journal
Accession number :
36451050
Full Text :
https://doi.org/10.1007/s10528-022-10306-4