Related Experiment Video
Updated: Mar 2, 2026

Microscopy-based Assays for High-throughput Screening of Host Factors Involved in Brucella Infection of Hela Cells
Published on: August 5, 2016
Brucella melitensis M5-90Δbp26 as a potential live vaccine that allows for the distinction between natural infection
Tiansen Li1, Zhixia Tong1, Meiling Huang2
1a College of Animal Science and Technology, Shihezi University, 832000, Shihezi, Xinjiang, People's Republic of China.
Abstract:
Brucella is Gram-negative intracellular bacterial pathogen that infects humans and animals and contributes to great economic losses in developing countries. Presently, live attenuated Brucella vaccines (Brucella melitensis M5-90) are the most effective means of brucellosis control and prevention in animals. However, these vaccines have several drawbacks, such as an inability to distinguish between a natural infection and immunization and an association with abortions in pregnant animals. Therefore, this study constructed a Brucella M5-90Δbp26 mutant and evaluated its virulence. The survival of the M5-90Δbp26 mutant was attenuated in human placenta trophoblastic 8 cells (HPT-8 cells) and in BALB/c mice, with a high immunoprotectivity noted in mice. Furthermore, safety tests showed that the M5-90Δbp26 mutant was less virulent than the M5-90 vaccine strain. Additionally, an indirect enzyme-linked immunosorbent assay (ELISA) screening was shown to detect the presence of Brucella protein 26 (BP26) with high sensitivity, with M5-90Δbp26 inoculation accompanied with a lack of BP26 expression, and was further confirmed by western blotting. Together, the M5-90Δbp26 mutant and the indirect ELISA can be employed to distinguish vaccinated livestock from infected animals.
Insights
A new Brucella vaccine mutant, M5-90Δbp26, shows reduced virulence and high immunoprotection in animal models. This mutant, along with an indirect ELISA test, can differentiate between vaccinated and infected animals, improving brucellosis control.
Area of Science:
- Veterinary microbiology
- Bacterial pathogenesis
- Vaccine development
Background:
- Brucella is a Gram-negative intracellular bacterium causing significant economic losses globally.
- Live attenuated Brucella vaccines like Brucella melitensis M5-90 are effective but have limitations.
- Current vaccines hinder distinguishing between natural infection and immunization and can cause abortions.
Purpose of the Study:
- To construct and evaluate the virulence and immunogenicity of a Brucella M5-90Δbp26 mutant.
- To assess the safety of the M5-90Δbp26 mutant compared to the parent vaccine strain.
- To develop a method for differentiating vaccinated animals from infected ones.
Main Methods:
- Construction of the Brucella M5-90Δbp26 mutant.
- In vitro survival assays in human placenta trophoblastic 8 cells (HPT-8 cells).
- In vivo virulence and immunoprotection studies in BALB/c mice.
- Safety evaluation of the mutant compared to the M5-90 strain.
- Development and validation of an indirect enzyme-linked immunosorbent assay (ELISA) for Brucella protein 26 (BP26) detection.
Main Results:
- The M5-90Δbp26 mutant exhibited attenuated survival in HPT-8 cells and BALB/c mice.
- The mutant demonstrated high immunoprotective efficacy in mice.
- Safety tests confirmed the M5-90Δbp26 mutant is less virulent than the M5-90 vaccine.
- An indirect ELISA successfully detected BP26 with high sensitivity.
- M5-90Δbp26 inoculation resulted in a lack of BP26 expression, confirmed by western blotting.
Conclusions:
- The Brucella M5-90Δbp26 mutant is a promising candidate for a safer and more effective brucellosis vaccine.
- The combination of the M5-90Δbp26 mutant and indirect ELISA allows for accurate differentiation between vaccinated and infected animals.
- This approach can significantly improve brucellosis surveillance and control strategies in livestock.
More Related Videos
12:53Cell-Free Scaled Production and Adjuvant Addition to a Recombinant Major Outer Membrane Protein from Chlamydia muridarum for Vaccine Development
Published on: March 16, 2022
06:32Protective Efficacy and Pulmonary Immune Response Following Subcutaneous and Intranasal BCG Administration in Mice
Published on: September 19, 2016