Protection of mice infected with Plasmodium berghei by Bacillus thuringiensis crystal proteins

Zhaohui Xu1, Baoan Yao, Ming Sun

  • 1College of Life Science and Technology, Huazhong Agricultural University, State Key Laboratory of Agricultural Microbiology, Hubei 430070 Wuhan, China.

Parasitology Research
|November 6, 2003
PubMed

Insights

Crystal proteins from Bacillus thuringiensis extended mouse survival against Plasmodium berghei by up to 5 days. These proteins protected red blood cells from parasite damage, suggesting a new malaria control strategy.

Area of Science:

  • Microbiology
  • Parasitology
  • Biochemistry

Background:

  • Plasmodium berghei is a parasite that causes malaria in mice.
  • Malaria is a significant global health concern.
  • Bacillus thuringiensis produces crystal proteins with insecticidal properties.

Purpose of the Study:

  • To investigate the anti-Plasmodium berghei activity of Bacillus thuringiensis crystal proteins.
  • To determine if these proteins can protect erythrocytes from parasite-induced damage.
  • To explore a novel therapeutic approach for malaria.

Main Methods:

  • Eight Bacillus thuringiensis strains were cultured and their crystal proteins extracted.
  • Crystal proteins were injected intravenously into Plasmodium berghei-infected mice.
  • Erythrocyte morphology and survival rates were analyzed using blood-cell staining and survival time measurements.
  • Protein composition was analyzed via electrophoresis.

Main Results:

  • Injection of crystal proteins from seven strains (007, 017, 020, 021, 030, 032, 037) extended mouse survival by 5 days (from 8.5 to 13.5-15 days).
  • Crystal proteins protected erythrocytes from swelling, shape loss, and lysis caused by Plasmodium berghei.
  • Most proteins were homologous to known crystal proteins, with strain 020 containing a unique 120-kDa surface-layer protein.

Conclusions:

  • Bacillus thuringiensis crystal proteins exhibit significant anti-Plasmodium berghei activity.
  • These proteins offer protection to erythrocytes, mitigating parasite-induced damage.
  • This research presents a potential new strategy for controlling plasmodial infections and malaria.