Identification of a conserved gene family with an essential role in <i>Leishmania</i> parasite–insect vector adhesion

B Barrack O. Owino (Department of Biological and Medical Sciences, Oxford Brookes University) R Ryuji Yanase (Department of Biological and Medical Sciences, Oxford Brookes University) K Katerina Pruzinova (Department of Parasitology, Charles University, Faculty of Science) H Helen Farr (Sir William Dunn School of Pathology, University of Oxford) Y Yaimie Lopez (Department of Biological and Medical Sciences, Oxford Brookes University) A Alan O. Marron (Department of Biological and Medical Sciences, Oxford Brookes University) S Sue Vaughan (Department of Biological and Medical Sciences, Oxford Brookes University) P Petr Volf (Department of Parasitology, Charles University, Faculty of Science) J Jack D. Sunter (Department of Biological and Medical Sciences, Oxford Brookes University)

Abstract

Adhesion to tissues and surfaces is used by pathogens to avoid clearance, maintain infections, and facilitate transmission. An important example is the adhesion of the Leishmania parasite to the stomodeal valve of its insect vector, the sand fly, which is important for life cycle progression, and occurs through its flagellum via a cytoskeletal adhesion complex. While three essential kinetoplastid-insect adhesion proteins (KIAPs) are known, the overall proteome of the adhesion complex is obscure. Using TurboID-tagged KIAP3 combined with proteomics and light microscopy, we have identified additional proteins associated with the adhered flagellum, including multiple members of the Adhesion Related NTPase-like Domain (ARND) family, of which the canonical member is KIAP4, described here. Phylogenetic analysis of the ARND family showed it is conserved across the kinetoplastids, and we demonstrate that Trypanosoma congolense paralogs localize to the adhered flagellum in that parasite. Deletion of KIAP4 severely impaired haptomonad adhesion, with the mutant parasites unable to colonize the sand fly stomodeal valve. Our work provides details of the molecular machinery essential for vector colonization and shows that these proteins have a conserved function in other kinetoplastid parasites.

Article Details

Volume / Issue Vol. 123, Issue 30
Published July 28, 2026
ISSN 0027-8424
Publisher National Academy of Sciences

Authors (9)

B

Barrack O. Owino

Department of Biological and Medical Sciences, Oxford Brookes University

R

Ryuji Yanase

Department of Biological and Medical Sciences, Oxford Brookes University

K

Katerina Pruzinova

Department of Parasitology, Charles University, Faculty of Science

H

Helen Farr

Sir William Dunn School of Pathology, University of Oxford

Y

Yaimie Lopez

Department of Biological and Medical Sciences, Oxford Brookes University

A

Alan O. Marron

Department of Biological and Medical Sciences, Oxford Brookes University

S

Sue Vaughan

Department of Biological and Medical Sciences, Oxford Brookes University

P

Petr Volf

Department of Parasitology, Charles University, Faculty of Science

J

Jack D. Sunter

Department of Biological and Medical Sciences, Oxford Brookes University