scholarly journals Identification of Plasmodium falciparum antigens by antigenic analysis of genomic and proteomic data

2003 ◽  
Vol 100 (17) ◽  
pp. 9952-9957 ◽  
Author(s):  
D. L. Doolan ◽  
S. Southwood ◽  
D. A. Freilich ◽  
J. Sidney ◽  
N. L. Graber ◽  
...  
2015 ◽  
Vol 83 (11) ◽  
pp. 4229-4236 ◽  
Author(s):  
Jeff Skinner ◽  
Chiung-Yu Huang ◽  
Michael Waisberg ◽  
Philip L. Felgner ◽  
Ogobara K. Doumbo ◽  
...  

ABSTRACTMalaria elimination efforts would benefit from vaccines that block transmission ofPlasmodium falciparumgametocytes from humans to mosquitoes. A clear understanding of gametocyte-specific antibody responses in exposed populations could help determine whether transmission-blocking vaccines (TBV) would be boosted by natural gametocyte exposure, and also inform the development of serologic tools to monitor gametocyte exposure in populations targeted for malaria elimination. To this end, plasma was collected from Malian children and adults before and after the 6-month malaria season and probed against a microarray containing 1,204P. falciparumproteins. Using publicly available proteomic data, we classified 91 proteins as gametocyte specific and 69 as proteins not expressed by gametocytes. The overall breadth and magnitude of gametocyte-specific IgG responses increased during the malaria season, although they were consistently lower than IgG responses to nongametocyte antigens. Notably, IgG specific for the TBV candidates Pfs48/45 and Pfs230 increased during the malaria season. In addition, IgGs specific for the gametocyte proteins Pfmdv1, Pfs16, PF3D7_1346400, and PF3D7_1024800 were detected in nearly all subjects, suggesting that seroconversion to these proteins may be a sensitive indicator of gametocyte exposure, although further studies are needed to determine the specificity and kinetics of these potential serologic markers. These findings suggest that TBV-induced immunity would be boosted through natural gametocyte exposure, and that antibody responses to particular antigens may reliably indicate gametocyte exposure.


Author(s):  
Mengquan Yang ◽  
Xiaomin Shang ◽  
Yiqing Zhou ◽  
Changhong Wang ◽  
Guiying Wei ◽  
...  

Malaria, an infectious disease caused by Plasmodium parasites, still accounts for amounts of deaths annually in last decades. Despite the significance of Plasmodium falciparum as a model organism of malaria parasites, our understanding of gene expression of this parasite remains largely elusive since lots of progress on its genome and transcriptome are based on assembly with short sequencing reads. Herein, we report the new version of transcriptome dataset containing all full-length transcripts over the whole asexual blood stages by adopting a full-length sequencing approach with optimized experimental conditions of cDNA library preparation. We have identified a total of 393 alternative splicing (AS) events, 3,623 long non-coding RNAs (lncRNAs), 1,555 alternative polyadenylation (APA) events, 57 transcription factors (TF), 1,721 fusion transcripts in P. falciparum. Furthermore, the shotgun proteome was performed to validate the full-length transcriptome of P. falciparum. More importantly, integration of full-length transcriptomic and proteomic data identified 160 novel small proteins in lncRNA regions. Collectively, this full-length transcriptome dataset with high quality and accuracy and the shotgun proteome analyses shed light on the complex gene expression in malaria parasites and provide a valuable resource for related functional and mechanistic researches on P. falciparum genes.


Author(s):  
D.J.P. Ferguson ◽  
A.R. Berendt ◽  
J. Tansey ◽  
K. Marsh ◽  
C.I. Newbold

In human malaria, the most serious clinical manifestation is cerebral malaria (CM) due to infection with Plasmodium falciparum. The pathology of CM is thought to relate to the fact that red blood cells containing mature forms of the parasite (PRBC) cytoadhere or sequester to post capillary venules of various tissues including the brain. This in vivo phenomenon has been studied in vitro by examining the cytoadherence of PRBCs to various cell types and purified proteins. To date, three Ijiost receptor molecules have been identified; CD36, ICAM-1 and thrombospondin. The specific changes in the PRBC membrane which mediate cytoadherence are less well understood, but they include the sub-membranous deposition of electron-dense material resulting in surface deformations called knobs. Knobs were thought to be essential for cytoadherence, lput recent work has shown that certain knob-negative (K-) lines can cytoadhere. In the present study, we have used electron microscopy to re-examine the interactions between K+ PRBCs and both C32 amelanotic melanoma cells and human umbilical vein endothelial cells (HUVEC).We confirm previous data demonstrating that C32 cells possess numerous microvilli which adhere to the PRBC, mainly via the knobs (Fig. 1). In contrast, the HUVEC were relatively smooth and the PRBCs appeared partially flattened onto the cell surface (Fig. 2). Furthermore, many of the PRBCs exhibited an invagination of the limiting membrane in the attachment zone, often containing a cytoplasmic process from the endothelial cell (Fig. 2).


1981 ◽  
Vol 46 (02) ◽  
pp. 547-549 ◽  
Author(s):  
E M Essien ◽  
M I Ebhota

SummaryDuring acute malaria infection, platelets in human platelet-rich plasma are hypersensitive to the addition of ADP between 1.0 uM and 5.0 uM, or adrenaline 0.11 uM as aggregating agents. The mean maximum aggregation amplitude (as % of light transmission) obtained from 8 subjects in response to added ADP (1.0 uM), 39.8 ± 27 (1SD), was significantly greater than the value in 6 controls (5.2±6.7 (1SD); t = 3, 51 P <0.005). A similar pattern of response was obtained with higher ADP concentrations (2.4,4.5 or 5.0 uM) in 22 patients and 20 control subjects (89.9±14.9% vs 77.8±16.5% (1SD) t = 2.45, P <0.02). Addition of 4.5 uM ADP to patient PRP usually evoked only a single aggregation wave (fused primary and secondary waves) while the typical primary and secondary wave pattern was usually obtained from controls.Mean plasma B-thromboglobulin (BTG) concentration in 7 patients (208.3 ± 15.6 ng/ml) was significantly higher than the value in 6 control subjects (59.2±15.7 ng/ml; t = 13.44, P <0.002).


2018 ◽  
Vol 18 (05) ◽  
pp. 332-338
Author(s):  
C. Kleine ◽  
U. Ziegler ◽  
E.-M. Schwienhorst ◽  
A. Stich

ZusammenfassungDer folgende Artikel fokussiert auf Erkrankungen, deren Erreger von Vektoren (Insekten, Spinnentieren) aktiv auf den Menschen übertragen werden. Sie spielen in tropischen und subtropischen Regionen der Erde eine erhebliche Rolle und sind auch im Rahmen der Differenzialdiagnose bei kranken Reiserückkehrern von großer Bedeutung. Am wichtigsten ist die Malaria, insbesondere die lebensbedrohliche Malaria tropica durch Plasmodium falciparum. Jede fieberhafte Erkrankung aus den Tropen erfordert eine zeitnahe Malaria-Diagnostik. Tropische Viruserkrankungen durch Dengue-, West-Nil-, Chikungunya- oder Zika-Viren haben sich in den vergangenen Jahrzehnten massiv ausgebreitet und stellen auch eine zunehmende Bedrohung für den europäischen Raum dar. Andere Vektor-übertragene Erkrankungen sind zwar von großer lokaler Relevanz in endemischen Regionen, aber als importierte Infektionen in Deutschland relativ selten. Bei der Betreuung der Patienten empfiehlt sich eine enge Kooperation mit Tropenmedizinern.


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