Noncanonical Vancomycin Resistance Cluster from Desulfitobacterium hafniense Y51

被引:7
作者
Kalan, Lindsay [1 ]
Ebert, Sara [2 ]
Kelly, Tom [3 ]
Wright, Gerard D. [1 ]
机构
[1] McMaster Univ, Michael G DeGroote Inst Infect Dis Res, Dept Biochem & Biomed Sci, Hamilton, ON L8N 3Z5, Canada
[2] Univ Alberta, Dept Biol Sci, Edmonton, AB, Canada
[3] St Josephs Hlth Care, Dept Microbiol, Hamilton, ON, Canada
基金
加拿大健康研究院;
关键词
ENTEROCOCCUS-FAECIUM BM4147; GLYCOPEPTIDE RESISTANCE; PEPTIDOGLYCAN PRECURSORS; STREPTOMYCES-COELICOLOR; ANTIBIOTIC RESISTOME; ESCHERICHIA-COLI; VANA; GENES; PAENIBACILLUS; BIOSYNTHESIS;
D O I
10.1128/AAC.01408-08
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The glycopeptide vancomycin is a drug of last resort for infection with gram-positive organisms, and three genes are vital to resistance: vanH, vanA, and vanX. These genes are found in a vanHAX cluster, which is conserved across pathogenic bacteria, glycopeptide antibiotic producers, and other environmental bacteria. The genome sequence of the anaerobic, gram-positive, dehalogenating bacterium Desulfitobacterium hafniense Y51 revealed a predicted vanA homolog; however, it exists in a vanAWK-murFX cluster, unlike those of other vancomycin-resistant organisms. Using purified recombinant VanA from D. hafniense Y51, we determined its substrate specificity and found it to have a 42-fold preference for D-lactate over D-alanine, confirming its activity as a D-Ala-D-Lac ligase and its annotation as VanA. Furthermore, we showed that D. hafniense Y51 is highly resistant to vancomycin, with a MIC for growth of 64 mu g/ml. Finally, vanA(Dh) is expressed during growth in vancomycin, as demonstrated by reverse transcription-PCR. This finding represents a new glycopeptide antibiotic resistance gene cluster and expands the genetic diversity of resistance to this important class of antibiotic.
引用
收藏
页码:2841 / 2845
页数:5
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