z-logo
open-access-imgOpen Access
Expression and regulation of the ery operon of Brucella melitensis in human trophoblast cells
Author(s) -
Hui Zhang,
Dou Xiaoxia,
Zhiqiang Li,
Yu Zhang,
Jing Zhang,
Fei Guo,
Yuanzhi Wang,
Zhen Wang,
Tiansen Li,
Xinli Gu,
Chuangfu Chen
Publication year - 2016
Publication title -
experimental and therapeutic medicine
Language(s) - English
Resource type - Journals
eISSN - 1792-1015
pISSN - 1792-0981
DOI - 10.3892/etm.2016.3688
Subject(s) - brucella , operon , biology , erythritol , brucella melitensis , microbiology and biotechnology , trophoblast , gene , brucellosis , genetics , placenta , virology , fetus , mutant , pregnancy , food science
Brucellosis is primarily a disease of domestic animals in which the bacteria localizes to fetal tissues such as embryonic trophoblast cells and fluids containing erythritol, which stimulates Brucella spp . growth. The utilization of erythritol is a characteristic of the genus Brucella . The ery operon contains four genes ( eryA , eryB , eryC and eryD ) for the utilization of erythritol, and plays a major role in the survival and multiplication of Brucella spp . The objective of the present study was to conduct a preliminary characterization of differential genes expression of the ery operon at several time points after Brucella infected embryonic trophoblast cells (HPT-8 cells). The result showed that the ery operon expression was higher in HPT-8 cells compared with the medium. The relative expression of eryA , eryB and eryC peaked at 2 h post-infection in HPT-8 cells, and eryD expression peaked at 3 h post-infection. The expression of eryA , eryB and eryC may be inhibited by increased eryD expression. However, the expression of the ery operon was stable in the presence of erythritol in cells. 2308Δ ery and 027Δ ery mutants of the ery operon were successfully constructed by homologous recombination, which were attenuated in RAW 264.7 murine macrophages. The characterization of the ery operon genes and their expression profiles in response to Brucella infection further contributes to our understanding of the molecular mechanisms of infection and the pathogenesis of brucellosis.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom