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dc.contributor.authorM. Markowitz, Lindsey
dc.contributor.authorNearman, Anthony
dc.contributor.authorZhao, Zexuan
dc.contributor.authorBoncristiani, Dawn
dc.contributor.authorButenko, Anzhelika
dc.contributor.authorPablos Torró, Luis Miguel de 
dc.contributor.authorMarin Alguacil, Arturo
dc.contributor.authorXu, Guang
dc.contributor.authorMachado, Carlos A.
dc.contributor.authorS. Schwarz, Ryan
dc.contributor.authorPalmer-Young, Evan C.
dc.contributor.authorEvans, Jay D.
dc.date.accessioned2025-01-07T10:11:09Z
dc.date.available2025-01-07T10:11:09Z
dc.date.issued2024-11-06
dc.identifier.citationM. Markowitz, L. et. al. G3, 2024, jkae258, [https://doi.org/10.1093/g3journal/jkae258]es_ES
dc.identifier.urihttps://hdl.handle.net/10481/98450
dc.description.abstractLotmaria 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.es_ES
dc.description.sponsorshipU.S. Department of Agriculture National Institute of Food and Agriculture Grant 2020-67013-31861es_ES
dc.description.sponsorshipDepartment of Agriculture National Institute of Food and Agriculture Postdoctoral Fellowship 2022-67012-37482es_ES
dc.description.sponsorshipDepartment of Agriculture Agricultural Research Service Beltsville Bee Research Laboratory in-house fundses_ES
dc.description.sponsorshipNational Science Foundation Grant DEB-2225083es_ES
dc.description.sponsorshipU.S. National Science Foundation Graduate Research Fellowship Program under Grant No. DGE-2236417es_ES
dc.language.isoenges_ES
dc.publisherOxford University Presses_ES
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectLotmaria passim strain BRLes_ES
dc.subjectATCC PRA-422es_ES
dc.subjectLeishmaniinaees_ES
dc.titleSomy evolution in the honey bee infecting trypanosomatid parasite Lotmaria passimes_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doi10.1093/g3journal/jkae258
dc.type.hasVersionVoRes_ES


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Atribución 4.0 Internacional
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