Back

Expression of the MSPDBL2 antigen in a discrete subset of Plasmodium falciparum schizonts is regulated by GDV1 but not linked to sexual commitment

Freville, A.; Stewart, L. B.; Tetteh, K. K.; Treeck, M.; Cortes, A.; Voss, T. S.; Tarr, S. J.; Baker, D. A.; Conway, D.

2023-11-21 microbiology
10.1101/2023.11.21.568010 bioRxiv
Show abstract

The Plasmodium falciparum merozoite surface protein MSPDBL2 is a polymorphic antigen targeted by acquired immune responses, and normally expressed in only a minority of mature schizonts. The potential relationship of MSPDBL2 to sexual commitment is examined, as variable mspdbl2 transcript levels and proportions of MSPDBL2-positive mature schizonts in clinical isolates have previously correlated with levels of many sexual stage parasite gene transcripts, although not with the master regulator ap2-g. It is demonstrated that conditional overexpression of GDV1, which promotes sexual commitment, also substantially increases the proportion of MSPDBL2-positive schizonts in culture. Conversely, truncation of the gdv1 gene is shown to prevent any expression of MSPDBL2. However, across diverse P. falciparum cultured lines the variable proportions of MSPDBL2 positivity in schizonts does not correlate significantly with variable gametocyte conversion rates, indicating it is not involved in sexual commitment. Confirming this, examining a line with endogenous HA-tagged AP2-G showed that the individual schizonts expressing MSPDBL2 are mostly different to those expressing AP2-G. Using a selection-linked integration system, modified P. falciparum lines were engineered to express an intact or disrupted version of MSPDBL2, showing the protein is not required for sexual commitment or early gametocyte development. Asexual parasite multiplication rates were also not affected by expression of either intact or disrupted MSPDBL2 in a majority of schizonts. Occurring alongside sexual commitment, the role of the discrete MSPDBL2-positive schizont subpopulation requires further investigation in natural infections where it is under immune selection.

Matching journals

The top 7 journals account for 50% of the predicted probability mass.

1
PLOS Pathogens
721 papers in training set
Top 1%
10.0%
2
Scientific Reports
3102 papers in training set
Top 8%
9.1%
3
Frontiers in Cellular and Infection Microbiology
98 papers in training set
Top 0.2%
8.2%
4
mBio
750 papers in training set
Top 2%
6.8%
5
PLOS ONE
4510 papers in training set
Top 28%
6.3%
6
mSphere
281 papers in training set
Top 0.6%
6.3%
7
Cellular Microbiology
18 papers in training set
Top 0.1%
4.8%
50% of probability mass above
8
Nature Communications
4913 papers in training set
Top 39%
3.6%
9
Frontiers in Microbiology
375 papers in training set
Top 3%
3.6%
10
Malaria Journal
48 papers in training set
Top 0.6%
3.6%
11
Peer Community Journal
254 papers in training set
Top 1%
2.6%
12
Frontiers in Immunology
586 papers in training set
Top 4%
1.8%
13
PLOS Neglected Tropical Diseases
378 papers in training set
Top 3%
1.7%
14
Parasitology
10 papers in training set
Top 0.1%
1.7%
15
Antimicrobial Agents and Chemotherapy
167 papers in training set
Top 1%
1.7%
16
The Journal of Infectious Diseases
182 papers in training set
Top 3%
1.5%
17
Molecular Microbiology
66 papers in training set
Top 0.6%
1.3%
18
PLOS Genetics
756 papers in training set
Top 10%
1.3%
19
Journal of Virology
456 papers in training set
Top 2%
1.3%
20
Journal of The Royal Society Interface
189 papers in training set
Top 3%
1.2%
21
International Journal for Parasitology
21 papers in training set
Top 0.3%
0.9%
22
eLife
5422 papers in training set
Top 54%
0.9%
23
Cells
232 papers in training set
Top 5%
0.9%
24
Microbiology Spectrum
435 papers in training set
Top 5%
0.9%
25
FEBS Letters
42 papers in training set
Top 0.3%
0.8%
26
PLOS Computational Biology
1633 papers in training set
Top 23%
0.8%
27
International Journal of Molecular Sciences
453 papers in training set
Top 16%
0.7%
28
Virulence
21 papers in training set
Top 0.6%
0.7%
29
Gene
41 papers in training set
Top 3%
0.6%