Journal article icon

Journal article

Identification of transporters essential for survival of Leishmania promastigotes in the digestive tract of sand flies

Abstract:
Leishmania amastigotes ingested by female phlebotomine sand flies are exposed to a harsh and dynamic environment that differs markedly from the intracellular niche in the mammalian host in temperature, pH and nutrient availability. Membrane transporter proteins, channels and pumps play a crucial role in maintaining cellular physiology under changing environments. A systematic loss-of-function screen of the L. mexicana transporter deletion mutants in macrophage and mouse infections previously identified transporter genes important for the amastigote stage. To test which transporters are important for the promastigote stage in the insect vector, we measured the fitness of gene deletion mutants in Lu. longipalpis sand flies. Pooled libraries of different complexities, consisting of 71–317 barcoded parasite lines allowed for an estimation of the bottleneck size in experimental infections, providing a foundation for similar experimental bar-seq studies. The fitness of each mutant parasite line was measured by tracking population composition over a course of 9 days in the sand flies and compared with the growth fitness of promastigotes over 7 days in laboratory cultures. There was a high correlation of fitness scores in vitro and in vivo, but 34 mutants showed a loss of fitness only in vivo, including deletion mutants of vacuolar H + ATPase (V-ATPase) subunits. V-ATPase deletion mutants expressed low levels of the metacyclic-specific transcript sherp in vitro and failed to generate metacyclic promastigotes in sand flies, indicating that V-ATPase function is required for parasite differentiation and progression through the Leishmania life cycle.
Publication status:
Published
Peer review status:
Peer reviewed

Actions

Access Document

Publisher copy:
10.1371/journal.ppat.1014049

Authors

More by this author
Role:
Author
ORCID:
0000-0002-0432-2707
More by this author
Institution:
University of Oxford
Role:
Author
ORCID:
0000-0001-9363-654X
More by this author
Role:
Author
ORCID:
0000-0002-7961-291X
More by this author
Role:
Author
ORCID:
0000-0002-6967-2484


More from this funder
Funder identifier:
10.13039/501100001871
Grant:
UID/04413/2025
More from this funder
Funder identifier:
https://ror.org/00yjd3n13
Grant:
310030_220011
More from this funder
Funder identifier:
https://ror.org/029chgv08
Grant:
211075/Z/18/Z
More from this funder
Funder identifier:
https://ror.org/00snfqn58


Publisher:
Public Library of Science
Journal:
PLoS Pathogens More from this journal
Volume:
22
Issue:
3
Pages:
e1014049
Article number:
e1014049
Publication date:
2026-03-16
Acceptance date:
2026-02-28
DOI:
EISSN:
1553-7374
ISSN:
1553-7366


Language:
English
Keywords:
Pubs id:
2391738
Local pid:
pubs:2391738
Source identifiers:
3872823
Deposit date:
2026-03-20
ARK identifier:
This ORA record was generated from metadata provided by an external service. It has not been edited by the ORA Team.

Terms of use


Views and Downloads






If you are the owner of this record, you can report an update to it here: Report update to this record

TO TOP