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用肠炎沙门氏菌和李斯特菌属对大麦(大麦)进行定殖

Colonization of barley (Hordeum vulgare) with Salmonella enterica and Listeria spp.

作者信息

Kutter Stefan, Hartmann Anton, Schmid Michael

机构信息

GSF-National Research Center for Environment and Health, Department of Rhizosphere Biology, Institute of Soil Ecology, Neuherberg, Germany.

出版信息

FEMS Microbiol Ecol. 2006 May;56(2):262-71. doi: 10.1111/j.1574-6941.2005.00053.x.

Abstract

Colonization of barley plants by the food-borne pathogens Salmonella enterica serovar typhimurium and three Listeria spp. (L. monocytogenes, L. ivanovii, L. innocua) was investigated in a monoxenic system. Herbaspirillum sp. N3 was used as a positive control and Escherichia coli HB101 as a negative control for endophytic root colonization. Colonization of the plants was tested 1-4 weeks after inoculation by determination of CFU, specific PCR assays and fluorescence in situ hybridization (FISH) with fluorescently labelled oligonucleotide probes in combination with confocal laser scanning microscopy (CLSM). Both S. enterica strains were found as endophytic colonizers of barley roots and reached up to 2.3 x 10(6) CFU per g root fresh weight after surface sterilization. The three Listeria strains had 10-fold fewer cell numbers after surface sterilization on the roots and therefore were similar to the results of nonendophytic colonizers, such as E. coli HB101. The FISH/CSLM approach demonstrated not only high-density colonization of the root hairs and the root surface by S. enterica but also a spreading to subjacent rhizodermis layers and the inner root cortex. By contrast, the inoculated Listeria spp. colonized the root hair zone but did not colonize other parts of the root surface. Endophytic colonization of Listeria spp. was not observed. Finally, a systemic spreading of S. enterica to the plant shoot (stems and leaves) was demonstrated using a specific PCR analysis and plate count technique.

摘要

在单菌系统中研究了食源性病原体肠炎沙门氏菌鼠伤寒血清型以及三种李斯特菌属细菌(单核细胞增生李斯特菌、伊氏李斯特菌、无害李斯特菌)在大麦植株上的定殖情况。将草本螺旋菌属菌株N3用作内生菌根定殖的阳性对照,大肠杆菌HB101用作阴性对照。接种1至4周后,通过测定菌落形成单位(CFU)、特异性聚合酶链反应(PCR)分析以及使用荧光标记寡核苷酸探针结合共聚焦激光扫描显微镜(CLSM)的荧光原位杂交(FISH)技术来检测植株的定殖情况。发现两种肠炎沙门氏菌菌株均为大麦根的内生定殖菌,表面消毒后每克根鲜重可达2.3×10⁶CFU。三种李斯特菌菌株在根表面消毒后的细胞数量少10倍,因此与非内生定殖菌(如大肠杆菌HB101)的结果相似。FISH/CLSM方法不仅证明肠炎沙门氏菌在根毛和根表面有高密度定殖,还证明其扩散到了相邻的根皮层和根内皮层。相比之下,接种的李斯特菌属细菌定殖在根毛区,但未定殖在根表面的其他部位。未观察到李斯特菌属细菌的内生定殖情况。最后,使用特异性PCR分析和平板计数技术证明肠炎沙门氏菌可系统地扩散到植株地上部分(茎和叶)。

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