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@ARTICLE{WichersMisterek:601561,
author = {Wichers-Misterek, Jan Stephan and Binder, Annika M. and
Mesen-Ramirez, Paolo and Dorner, Lilian Patrick and Safavi,
Soraya and Fuchs, Gwendolin and Lenz, Tobias L. and
Bachmann, Anna and Wilson, Danny and Frischknecht, Friedrich
and Gilberger, Tim},
title = {{A} {M}icrotubule-{A}ssociated {P}rotein {I}s {E}ssential
for {M}alaria {P}arasite {T}ransmission},
journal = {mBio},
volume = {14},
number = {1},
issn = {2161-2129},
address = {Washington, DC},
publisher = {American Society for Microbiology},
reportid = {PUBDB-2024-00270},
pages = {e03318-22},
year = {2023},
note = {L.P.D., and F.F. were supported by DFG (SPP 2332, Physics
of Parasitism; FR 2140 13-1), SFB 1129, and FR 2140/10-1.
T.L.L. was supported by the DFG, 437857095. This work was
partially supported by the German Research Foundation
(SPP2225) and the HamburgX project grant. D.W. is supported
by the Humboldt Foundation.},
abstract = {Mature gametocytes of Plasmodium falciparum display a
banana (falciform) shape conferred by a complex array of
subpellicular microtubules (SPMT) associated with the inner
membrane complex (IMC). Microtubule-associated proteins
(MAPs) define MT populations and modulate interaction with
pellicular components. Several MAPs have been identified in
Toxoplasma gondii, and homologues can be found in the
genomes of Plasmodium species, but the function of these
proteins for asexual and sexual development of malaria
parasites is still unknown. Here, we identified a novel
subpellicular MAP, termed SPM3, that is conserved within the
genus Plasmodium, especially within the subgenus Laverania,
but absent in other Apicomplexa. Conditional knockdown and
targeted gene disruption of Pfspm3 in Plasmodium falciparum
cause severe morphological defects during gametocytogenesis,
leading to round, nonfalciform gametocytes with an aberrant
SPMT pattern. In contrast, Pbspm3 knockout in Plasmodium
berghei, a species with round gametocytes, caused no defect
in gametocytogenesis, but sporozoites displayed an aberrant
motility and a dramatic defect in invasion of salivary
glands, leading to a decreased efficiency in transmission.
Electron microscopy revealed a dissociation of the SPMT from
the IMC in Pbspm3 knockout parasites, suggesting a function
of SPM3 in anchoring MTs to the IMC. Overall, our results
highlight SPM3 as a pellicular component with essential
functions for malaria parasite transmission.},
cin = {CSSB-BNITM-TG},
ddc = {570},
cid = {I:(DE-H253)CSSB-BNITM-TG-20210520},
pnm = {899 - ohne Topic (POF4-899) / DFG project
G:(GEPRIS)437857095 - Evolutionäre Genetik und Dynamiken in
der Antigenpräsentation und -erkennung des adaptiven
Immunsystems (437857095) / DFG project G:(GEPRIS)441960173 -
SPP 2332: Physik des Parasitismus (441960173) / DFG project
G:(GEPRIS)531703706 - Entschlüsselung der molekularen
Mechanismen des Austritts von Orientia tsutsugamushi aus der
Wirtszelle (531703706)},
pid = {G:(DE-HGF)POF4-899 / G:(GEPRIS)437857095 /
G:(GEPRIS)441960173 / G:(GEPRIS)531703706},
experiment = {EXP:(DE-MLZ)NOSPEC-20140101},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:36625655},
UT = {WOS:000912135300001},
doi = {10.1128/mbio.03318-22},
url = {https://bib-pubdb1.desy.de/record/601561},
}