Somy evolution in the honey bee infecting trypanosomatid parasite <i>Lotmaria passim</i>

Lotmaria passim is a ubiquitous trypanosomatid parasite of honey bees nestled within the medically important subfamily Leishmaniinae. Although this parasite is associated with honey bee colony losses, the original draft genome-which was completed before its differentiation from the closely related Crithidia mellificae-has remained the reference for this species despite lacking improvements from newer methodologies. Here, we report the updated sequencing, assembly, and annotation of the BRL-type (Bee Research Laboratory) strain (ATCC PRA-422) of Lotmaria passim. The nuclear genome assembly has been resolved into 31 complete chromosomes and is paired with an assembled kinetoplast genome consisting of a maxicircle and 30 minicircle sequences. The assembly spans 33.7 Mb and contains very little repetitive content, from which our annotation of both the nuclear assembly and kinetoplast predicted 10,288 protein-coding genes. Analyses of the assembly revealed evidence of a recent chromosomal duplication event within chromosomes 5 and 6 and provided evidence for a high level of aneuploidy in this species, mirroring the genomic flexibility employed by other trypanosomatids as a means of adaptation to different environments. This high-quality reference can therefore provide insights into adaptations of trypanosomatids to the thermally regulated, acidic, and phytochemically rich honey bee hindgut niche, which offers parallels to the challenges faced by other Leishmaniinae during the challenges they undergo within insect vectors, during infection of mammals, and exposure to antiparasitic drugs throughout their multi-host life cycles. This reference will also facilitate investigations of strain-specific genomic polymorphisms, their role in pathogenicity, and the development of treatments for pollinator infection.

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Publication Details

Journal
G3 Genes Genomes Genetics
Published
2024-11-06
DOI
https://doi.org/10.1093/g3journal/jkae258
Citations
2
Primary Topic
Insect and Pesticide Research
Type
article
Field-Weighted Citation Impact
1.08

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article

Somy evolution in the honey bee infecting trypanosomatid parasite Lotmaria passim

Jay D. Evans, Carlos A. Machado, Lindsey M. Markowitz, Dawn Boncristiani et al.
2 citations
G3 Genes Genomes Genetics
Insect and Pesticide Research
1.08
article

Somy evolution in the honey bee infecting trypanosomatid parasite Lotmaria passim

Jay D. Evans, Carlos A. Machado, Lindsey M. Markowitz, Dawn Boncristiani, Arturo Marín, Guang Xu, Ryan S. Schwarz, Anzhelika Butenko, Luis Miguel De Pablos, Anthony Nearman, Evan C. Palmer‐Young, Zexuan Zhao
article en
2 citations

Abstract

Lotmaria passim is a ubiquitous trypanosomatid parasite of honey bees nestled within the medically important subfamily Leishmaniinae. Although this parasite is associated with honey bee colony losses, the original draft genome-which was completed before its differentiation from the closely related Crithidia mellificae-has remained the reference for this species despite lacking improvements from newer methodologies. Here, we report the updated sequencing, assembly, and annotation of the BRL-type (Bee Research Laboratory) strain (ATCC PRA-422) of Lotmaria passim. The nuclear genome assembly has been resolved into 31 complete chromosomes and is paired with an assembled kinetoplast genome consisting of a maxicircle and 30 minicircle sequences. The assembly spans 33.7 Mb and contains very little repetitive content, from which our annotation of both the nuclear assembly and kinetoplast predicted 10,288 protein-coding genes. Analyses of the assembly revealed evidence of a recent chromosomal duplication event within chromosomes 5 and 6 and provided evidence for a high level of aneuploidy in this species, mirroring the genomic flexibility employed by other trypanosomatids as a means of adaptation to different environments. This high-quality reference can therefore provide insights into adaptations of trypanosomatids to the thermally regulated, acidic, and phytochemically rich honey bee hindgut niche, which offers parallels to the challenges faced by other Leishmaniinae during the challenges they undergo within insect vectors, during infection of mammals, and exposure to antiparasitic drugs throughout their multi-host life cycles. This reference will also facilitate investigations of strain-specific genomic polymorphisms, their role in pathogenicity, and the development of treatments for pollinator infection.

G3 Genes Genomes GeneticsVol. 15(1)
Agricultural Research Service (US), Fort Lewis College (US), Universidad de Granada (ES), University of Ostrava (CZ), University of Massachusetts Amherst (US), University of South Bohemia in České Budějovice (CZ), Institute of Parasitology of the Slovak Academy of Sciences (SK), Complejo Hospitalario Universitario de Granada (ES), University of Maryland, College Park (US)
U.S. Department of Agriculture
Responsible consumption and production
Openalex Percentile: Top 21%
Insect and Pesticide Research
1.08
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