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Published on: May 30, 2019
Sudden increase in virulence in a strain of Plasmodium berghei yoelii
Abstract:
The mild and chronic 17X strain of Plasmodium berghei yoelii showed a sudden increase in virulence following a period of 110 days in the deep freeze. The enhanced virulence was seen in a very high and early parasite peak in the blood and a 100% mortality of all infected mice. The exalted virulence remained unaltered following a number of blood transfers of the strain and after four cyclical transmissions through Anopheles stephensi. Enzyme pattern studies revealed that the virulent strain possessed the enzyme types GPI-1 and 6 PGD-4,-both characteristic for strain 17X of P.b. yoelii. Studies carried out to investigate the possibility of a concomitant viral infection transferred by blood passage, which could have been responsible for the enhanced virulence and mortality in the infected mice, showed no presence of any detectable virus in the blood of the P.b. yoelii infected mice. It is suggested that virulence may provide a marker in genetic work of rodent plasmodia and be included in association with enzyme and drug resistance markers.
Insights
A Plasmodium berghei yoelii strain (17X) unexpectedly increased virulence after cryopreservation, causing high parasite levels and 100% mouse mortality. This enhanced virulence was stable and not due to viral co-infection.
Area of Science:
- Malariology
- Parasitology
- Molecular Biology
Background:
- The 17X strain of Plasmodium berghei yoelii is typically mild and chronic.
- Cryopreservation is a common method for preserving biological samples, including Plasmodium strains.
- Understanding factors influencing parasite virulence is crucial for malaria research.
Purpose of the Study:
- To investigate the sudden increase in virulence of the 17X strain of Plasmodium berghei yoelii after prolonged cryopreservation.
- To characterize the virulence phenotype and rule out confounding factors like viral co-infection.
- To explore the potential of virulence as a genetic marker in rodent malaria.
Main Methods:
- Cryopreservation of Plasmodium berghei yoelii strain 17X for 110 days.
- Infection of mice to assess virulence (parasitemia, mortality).
- Blood transfers and cyclical transmission through Anopheles stephensi to evaluate virulence stability.
- Enzyme typing (GPI-1, 6 PGD-4) to characterize the strain.
- Viral screening in infected mice.
Main Results:
- The cryopreserved 17X strain exhibited significantly enhanced virulence, characterized by high and early parasitemia and 100% mouse mortality.
- The enhanced virulence phenotype remained stable after serial blood passages and cyclical transmission.
- Enzyme typing confirmed the strain as characteristic of 17X, with GPI-1 and 6 PGD-4 enzyme types.
- No detectable viral co-infection was found in the infected mice.
Conclusions:
- Cryopreservation can induce a stable increase in Plasmodium berghei yoelii virulence.
- Virulence in rodent malaria parasites may serve as a useful genetic marker.
- Virulence markers could be valuable in conjunction with enzyme and drug resistance markers for genetic studies.
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