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Summary
Rhomboid‐like proteases cleave membrane‐anchored proteins within their transmembrane domains. In apicomplexan parasites substrates include molecules that function in parasite motility and host cell invasion. While two
P
lasmodium
rhomboids,
ROM
1 and
ROM
4, have been examined, the roles of the remaining six rhomboids during the malaria parasite's life cycle are unknown. We present systematic gene deletion analyses of all eight
P
lasmodium
rhomboid‐like proteins as a means to discover stage‐specific phenotypes and potential functions in the rodent malaria model,
P
. berghei
. Four rhomboids (
ROM
4, 6, 7 and 8) are refractory to gene deletion, suggesting an essential role during asexual blood stage development. In contrast
ROM
1, 3, 9 and 10 were dispensable for blood stage development and exhibited no, subtle or severe defects in mosquito or liver development. Parasites lacking
ROM
9 and
ROM
10 showed no major phenotypic defects. Parasites lacking
ROM
1 presented a delay in blood stage patency following liver infection, but in contrast to a previous study blood stage parasites had similar growth and virulence characteristics as wild type parasites. Parasites lacking
ROM
3 in mosquitoes readily established oocysts but failed to produce sporozoites.
ROM
3 is the first apicomplexan rhomboid identified to play a vital role in sporogony.
Sprache
Englisch
Identifikatoren
ISSN: 0950-382X
eISSN: 1365-2958
DOI: 10.1111/mmi.12187
Titel-ID: cdi_crossref_primary_10_1111_mmi_12187
Format
–
Weiterführende Literatur
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