Effect of pre-existing Schistosoma haematobium infection on Plasmodium berghei multiplications in imprinting control region mice
| dc.contributor.author | Amoani, B. | |
| dc.contributor.author | Ameyaw, E.O. | |
| dc.contributor.author | Asante, D.-B. | |
| dc.contributor.author | Armah, F.A. | |
| dc.contributor.author | Prah, J. | |
| dc.contributor.author | Kwesi Botchey, C.P. | |
| dc.contributor.author | Boampong, J.N. | |
| dc.date.accessioned | 2019-02-15T09:16:04Z | |
| dc.date.available | 2019-02-15T09:16:04Z | |
| dc.date.issued | 2015-06 | |
| dc.description.abstract | Objective: To investigate the effect of pre-existing Schistosoma haematobium (S. haematobium) infection on malaria disease severity. Methods: The study involved the use of twenty-five imprinting control region mice, fifteen of which were initially infected with S. haematobium. Five of the remaining ten schisto-uninfected mice together with five schisto-infected mice were infected with Plasmodium berghei (P. berghei) after four weeks (acute stage) of schistosoma infection. The remaining five schisto-uninfected mice together with five schisto-infected mice were also infected with P. berghei after seven weeks (chronic stage) of schistosoma infection. The last five schisto-infected mice were used as control group. They were then monitored for changes in P. berghei parasitaemia on Days 3, 5, 7, 9 and 11 post-infection. Records on their survivability were also taken. Results: The co-infected mice had significantly higher malaria parasitaemia, compared with the mono-infected mice during acute S. haematobium infection. In contrast, the coinfected mice had significantly lower malaria parasitaemia during chronic S. haematobium infection and a higher survival rate. Conclusions: Co-infection of mice with P. berghei during acute S. haematobium infection resulted in rapid P. berghei development and increased malaria parasitaemia. However, the co-infection resulted in slower P. berghei development and decreased malaria parasitaemia with enhanced survivability of the mice during chronic S. haematobium infection. Therefore, pre-existing chronic S. haematobium infection may provide some protection to the host by reducing parasitaemia. © 2015 Hainan Medical University. | en_US |
| dc.identifier.other | https://doi.org/10.1016/j.apjtb.2015.03.007 | |
| dc.identifier.other | Volume 5, Issue 6, Pages 488-492 | |
| dc.identifier.uri | http://ugspace.ug.edu.gh/handle/123456789/27546 | |
| dc.language.iso | en | en_US |
| dc.publisher | Asian Pacific Journal of Tropical Biomedicine | en_US |
| dc.subject | Parasitaemia | en_US |
| dc.subject | Plasmodium berghei | en_US |
| dc.subject | Schistosoma haematobium | en_US |
| dc.subject | Survivability | en_US |
| dc.title | Effect of pre-existing Schistosoma haematobium infection on Plasmodium berghei multiplications in imprinting control region mice | en_US |
| dc.type | Article | en_US |
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