Journal article icon

Journal article

<i>Leishmania mexicana</i> pathogenicity requires flagellar assembly but not motility

Abstract:
Protists of the order Trypanosomatida possess a single multifunctional flagellum, which powers cellular displacement and mediates attachment to tissues of the arthropod vector. The kinetoplastid flagellar cytoskeleton consists of a nine-microtubule doublet axoneme; further structural elaborations, which can vary between species and life cycle stages, include the assembly of axonemal dynein complexes, a pair of singlet microtubules and the extra-axonemal paraflagellar rod. The intracellular amastigote forms of Leishmania spp. build a short, non-motile cilium whose function has remained enigmatic. Here, we used a panel of 25 barcoded promastigote cell lines, including mutants lacking genes encoding flagellar assembly proteins, axonemal proteins required for normal motility, or flagellar membrane proteins to examine how these defects impact on their virulence in macrophages and mice. Mutants lacking the intraflagellar transport (IFT) protein 88 were avirulent indicating that assembly of a flagellum is necessary to allow for Leishmania survival in a mammalian host. A similarly severe loss of virulence was observed upon deletion of BBS2, a core component of the BBSome complex, which may act as a cargo adapter for IFT. By contrast, promastigotes that were unable to beat their flagella due to loss of core axonemal proteins could establish and sustain an infection and only showed a small reduction of parasite burden in vivo compared to the parental cell lines. These results confirm that flagellar motility is not necessary for mammalian infection, but flagellum assembly and the integrity of the BBSome are essential for pathogenicity.
Publication status:
Published
Peer review status:
Peer reviewed

Actions

Access Document

Publisher copy:
10.1080/21505594.2025.2521478

Authors

More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Pathology Dunn School
Sub department:
Pathology Dunn School
Role:
Author
ORCID:
0000-0001-9117-2649
More by this author
Role:
Author
ORCID:
0000-0001-9756-546X
More by this author
Role:
Author
ORCID:
0000-0001-8983-3487
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Pathology Dunn School
Sub department:
Pathology Dunn School
Role:
Author
ORCID:
0000-0002-2403-0859
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Pathology Dunn School
Sub department:
Pathology Dunn School
Role:
Author
ORCID:
0000-0003-4346-0317


More from this funder
Funder identifier:
https://ror.org/029chgv08


Publisher:
Taylor and Francis Group
Journal:
Virulence More from this journal
Volume:
16
Issue:
1
Pages:
2521478
Publication date:
2025-07-02
Acceptance date:
2025-06-07
DOI:
EISSN:
2150-5608
ISSN:
2150-5594
Pmid:
40602995


Language:
English
Keywords:
Pubs id:
2268895
Local pid:
pubs:2268895
Source identifiers:
3109148
Deposit date:
2025-07-12
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