Distribution of specific tetracycline and erythromycin resistance genes in environmental samples assessed by macroarray detection

被引:69
作者
Patterson, Andrea J.
Colangeli, Roberto
Spigaglia, Patrizia
Scott, Karen P. [1 ]
机构
[1] Rowett Res Inst, Gut Hlth Div, Aberdeen AB21 9SB, Scotland
[2] Univ Med & Dent New Jersey, Ctr Emerging Pathogens, Newark, NJ 07103 USA
[3] Ist Super Sanita, Dept Infect Parasit & Immune Mediated Dis, I-00161 Rome, Italy
关键词
D O I
10.1111/j.1462-2920.2006.01190.x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A macroarray system was developed to screen environmental samples for the presence of specific tetracycline (Tc-R) and erythromycin (erm(R)) resistance genes. The macroarray was loaded with polymerase chain reaction (PCR) amplicons of 23 Tc-R genes and 10 erm(R) genes. Total bacterial genomic DNA was extracted from soil and animal faecal samples collected from different European countries. Macroarray hybridization was performed under stringent conditions and the results were analysed by fluorescence scanning. Pig herds in Norway, reared without antibiotic use, had a significantly lower incidence of antibiotic resistant bacteria than those reared in other European countries, and organic herds contained lower numbers of resistant bacteria than intensively farmed animals. The relative proportions of the different genes were constant across the different countries. Ribosome protection type Tc-R genes were the most common resistance genes in animal faecal samples, with the tet(W) gene the most abundant, followed by tet(O) and tet(Q). Different resistance genes were present in soil samples, where erm(V) and erm(E) were the most prevalent followed by the efflux type Tc-R genes. The macroarray proved a powerful tool to screen DNA extracted from environmental samples to identify the most abundant Tc-R and erm(R) genes within those tested, avoiding the need for culturing and biased PCR amplification steps.
引用
收藏
页码:703 / 715
页数:13
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