坦桑尼亚恩戈罗恩戈罗保护区和米库米国家公园野生有蹄类动物抗生素耐药基因的定量分析

A. Katakweba, J. E. Olsen
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引用次数: 0

摘要

野生动物可以作为耐药细菌的宿主,并在环境中转移耐药基因。这些基因既可以通过共有的耐药细菌直接传播给牲畜和人类,也可以通过水平基因转移给环境细菌。为了确定野生动物携带抗性基因的程度,从恩戈罗恩戈罗保护区(NCA)和米库米国家公园(MNP)采集了8份水牛、斑马和角马的粪便样本,并从与NCA野生动物一起放牧的当地斑马牛采集了4份对照样本。对四环素(tet(A)、tet(B)、93 tet(C)、tet(M)、tet(O)、tet(W)、大环内酯、lincosamide、链脲素B (ermB、ermF)、磺胺(sulI、sulII)、β -内酰胺(blaCTX-M-1组、blaCMY-2组、blaSHV组)和糖肽(vanA)等14个耐药基因进行qPCR检测。来自NCA、野生动物和牛的14个抗性基因中有8个呈阳性。最常见的基因是tet(W)和blaCMY-2,后者与编码esbl型抗性有关。在MNP中,布法罗未与牛发生相互作用的三个样本检测出tet(W)和blaCMY-2阳性,此外还有sulI阳性。这表明草原上的野生有蹄类动物,无论与牛接触与否,都可能构成抗菌素耐药性决定因素的储存库。野生动物耐药基因库的确定有待进一步研究
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Quantification of antibiotic resistance genes in wildlife ungulates in Ngorongoro Conservation area and Mikumi National Park, Tanzania
Wild-animals can act as reservoirs for resistant bacteria and transfer of resistance genes in the environment. These genes can spread to livestock and human either directly by transmission of shared resistant bacteria, or by horizontal gene-transfer to environmental bacteria. To ascertain at what extent wild-animals carry resistance genes, eight faecal samples from buffalo, zebra and wildebeest from Ngorongoro Conservation Area (NCA) and Mikumi National Park (MNP), and four control samples from local zebu cattle grazing together with wildlife in NCA. The qPCR was carried on 14 antimicrobial resistance genes including tetracycline (tet(A), tet(B), 93 tet(C), tet(M), tet(O), tet(W), macrolide, lincosamide, streptogramin B (ermB, ermF), sulphonamide (sulI, sulII), beta-lactam (blaCTX-M-1 group, blaCMY-2, blaSHV) and glycopeptide (vanA).  Samples from NCA, both wildlife and cattle were positive for 8 out of 14 resistance genes. The most prevalent genes were tet(W) and blaCMY-2 with the latter being of concern in encoding ESBL-type resistance. Three samples from Buffalo not interacting with cattle in MNP, were positive for tet(W) and blaCMY-2, and in addition for sulI. This suggests that wild ungulates on savannah, irrespective of contact with cattle, may constitute a reservoir for antimicrobial resistance determinants. Further studies are indicated to determine resistance gene-pool among wildlife animals
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