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. Author manuscript; available in PMC: 2008 Aug 1.
Published in final edited form as: Exp Parasitol. 2007 Feb 13;116(4):346–353. doi: 10.1016/j.exppara.2007.01.022

Table 3.

In vivo inhibition of P. berghei oocyst formation by gomesin

Exp. Gomesin concentration Oocysts per Midguta Oocyst-positive mosquitoesb % Oocyst inhibition
1 25 μM
control
72.1 (0–225)
131.4 (0–352)
93.3 (14/15)
91.7 (11/12)
45
2 50 μM
Control
14.5 (0–162) *
30.8 (0–122)
65.6 (21/32)
83.3 (25/30)
53
3 50 μM
Control
74.4 (0–244)*
375.8 (190–592)
94.1 (16/17)
100 (5/5)
80
4 100 μM
Control
2.4 (0–14)**
17.6 (0–72)
40 (14/35)
85.7 (30/35)
86
5 200 μM
Control
85.3 (3–188) *
274 (95–510)
100 (11/11)
100 (5/5)
69
6 200 μM
Control
19.2 (0–92) *
65.7 (0–284)
97 (33/34)
81.3 (26/32)
70

For each experiment, control An. stephensi mosquitoes were fed on anaesthetized P. berghei-infected mouse. A second group of experimental mosquitoes was fed on the same mouse about 10 min after injection of gomesin into its tail vein. Mosquitoes were kept at 21°C and the number of oocysts per midgut was determined on day 15. Data from 6 independent experiments.

a

Mean oocyst number per mosquito midgut. The range of observed values is indicated in parentheses.

b

Percentage of mosquitoes that had oocysts in their midgut. These values were derived from the number of oocyst-positive mosquitoes over the total number of mosquitoes examined (shown in parentheses).

*

p<0.05;

**

p<0.0001 in comparison to the control by the Mann-Whitney test.