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幽门螺杆菌hspA基因在乳酸乳球菌NICE系统中的表达及其免疫反应性实验研究

Expression of Helicobacter pylori hspA Gene in Lactococcus lactis NICE System and Experimental Study on Its Immunoreactivity.

作者信息

Zhang Xiao-Juan, Feng Shu-Ying, Li Zhi-Tao, Feng Yan-Ming

机构信息

Department of Pathogen Biology, Medical College, Henan University of Science and Technology, Luoyang 471003, China.

Department of Immunology, Medical College, Henan University of Science and Technology, Luoyang 471003, China.

出版信息

Gastroenterol Res Pract. 2015;2015:750932. doi: 10.1155/2015/750932. Epub 2015 Apr 22.

Abstract

Aim. The aim of this study was to develop an oral Lactococcus lactis (L. lactis) vaccine against Helicobacter pylori (H. pylori). Methods. After L. lactis NZ3900/pNZ8110-hspA was constructed, growth curves were plotted to study whether the growth of recombinant L. lactis was affected after hspA was cloned into L. lactis and whether the growth of empty bacteria, empty plasmid bacteria, and recombinant L. lactis was affected by different concentrations of Nisin; SDS-PAGE and Western blot were adopted, respectively, to detect the HspA expressed by recombinant L. lactis and its immunoreactivity. Results. There was no effect observed from the growth curve after exogenous gene hspA was cloned into L. lactis NZ3900; different concentrations of Nisin did not affect the growth of NZ3900 and NZ3900/pNZ8110, while different concentrations of Nisin inhibited the growth of NZ3900/pNZ8110-hspA except 10 ng/mL Nisin. No HspA strip was observed from SDS-PAGE. Western blot analysis showed that HspA expressed by recombinant bacteria had favorable immunoreactivity. Conclusion. The growth of recombinant L. lactis was suppressed even though a small amount of HspA had been induced to express. Therefore recombinant L. lactis only express HspA which was not suitable to be oral vaccine against Helicobacter pylori.

摘要

目的。本研究旨在研发一种针对幽门螺杆菌(H. pylori)的口服乳酸乳球菌(L. lactis)疫苗。方法。构建乳酸乳球菌NZ3900/pNZ8110-hspA后,绘制生长曲线以研究将hspA克隆到乳酸乳球菌后重组乳酸乳球菌的生长是否受到影响,以及空菌、空质粒菌和重组乳酸乳球菌的生长是否受到不同浓度的乳酸链球菌素的影响;分别采用SDS-PAGE和蛋白质免疫印迹法检测重组乳酸乳球菌表达的HspA及其免疫反应性。结果。将外源基因hspA克隆到乳酸乳球菌NZ3900后,生长曲线未观察到影响;不同浓度的乳酸链球菌素不影响NZ3900和NZ3900/pNZ8110的生长,而除10 ng/mL乳酸链球菌素外,不同浓度的乳酸链球菌素均抑制NZ3900/pNZ8110-hspA的生长。SDS-PAGE未观察到HspA条带。蛋白质免疫印迹分析表明重组菌表达的HspA具有良好的免疫反应性。结论。即使诱导表达了少量的HspA,重组乳酸乳球菌的生长仍受到抑制。因此重组乳酸乳球菌仅表达HspA,不适合作为针对幽门螺杆菌的口服疫苗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9dc/4421100/0f9375efe96b/GRP2015-750932.001.jpg

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