Evidence map›Paper›PMID 37032389›Full record

ArticleBMC biology2023

Phylogenomics revealed migration routes and adaptive radiation timing of Holarctic malaria mosquito species of the Maculipennis Group.

Andrey A Yurchenko, Anastasia N Naumenko, Gleb N Artemov, Dmitry A Karagodin, James M Hodge, Alena I Velichevskaya, Alina A Kokhanenko, Semen M Bondarenko, Mohammad R Abai, Maryam Kamali and 8 more

Open access · goldAbstract read
In one paragraph

Article in BMC biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.2field-weighted citation impact, top 22% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors at 8 institutions in 6 countries.

Andrey A YurchenkoDepartment of Entomology, the Fralin Life Sciences Institute, Virginia Polytechnic Institute and State University, Blacksburg, VA, USA.
Anastasia N NaumenkoDepartment of Entomology, the Fralin Life Sciences Institute, Virginia Polytechnic Institute and State University, Blacksburg, VA, USA.
Gleb N ArtemovDepartment of Genetics and Cell Biology and the Laboratory of Ecology, Genetics and Environmental Protection, Tomsk State University, Tomsk, Russia.
Dmitry A KaragodinLaboratory of Cell Differentiation Mechanisms, the Federal Research Center, Institute of Cytology and Genetics, Novosibirsk, Russia.
James M HodgeDepartment of Entomology, the Fralin Life Sciences Institute, Virginia Polytechnic Institute and State University, Blacksburg, VA, USA.
Alena I VelichevskayaDepartment of Genetics and Cell Biology and the Laboratory of Ecology, Genetics and Environmental Protection, Tomsk State University, Tomsk, Russia.
Alina A KokhanenkoDepartment of Genetics and Cell Biology and the Laboratory of Ecology, Genetics and Environmental Protection, Tomsk State University, Tomsk, Russia.
Semen M BondarenkoDepartment of Entomology, the Fralin Life Sciences Institute, Virginia Polytechnic Institute and State University, Blacksburg, VA, USA.
Mohammad R AbaiDepartment of Medical Entomology and Vector Control, Tehran University of Medical Sciences, Tehran, Iran.
Maryam KamaliDepartment of Medical Entomology and Parasitology, Tarbiat Modares University, Tehran, Iran.
Mikhail I GordeevDepartment of General Biology and Ecology, State University of Education, Mytishchi, Russia.
Anton V MoskaevDepartment of General Biology and Ecology, State University of Education, Mytishchi, Russia.
Beniamino CaputoDipartimento Di Sanità Pubblica E Malattie Infettive, Università Sapienza, Rome, Italy.
Sargis A AghayanScientific Center of Zoology and Hydroecology, National Academy of Sciences of the Republic of Armenia, Yerevan, Armenia.
Elina M BarichevaLaboratory of Cell Differentiation Mechanisms, the Federal Research Center, Institute of Cytology and Genetics, Novosibirsk, Russia.
Vladimir N StegniyDepartment of Genetics and Cell Biology and the Laboratory of Ecology, Genetics and Environmental Protection, Tomsk State University, Tomsk, Russia.
Maria V SharakhovaDepartment of Entomology, the Fralin Life Sciences Institute, Virginia Polytechnic Institute and State University, Blacksburg, VA, USA. msharakh@vt.edu.
Igor V SharakhovDepartment of Entomology, the Fralin Life Sciences Institute, Virginia Polytechnic Institute and State University, Blacksburg, VA, USA. igor@vt.edu.ORCID 0000-0003-0752-3747
National Research Tomsk State University · RUInstitute of Cytology and Genetics · RUVirginia Tech · USInserm · FRSapienza University of Rome · ITTarbiat Modares University · IRTehran University of Medical Sciences · IRYerevan State University · AM

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPhylogenetic analyses of closely related species of mosquitoes are important for better understanding the evolution of traits contributing to transmission of vector-borne diseases. Six out of 41 dominant malaria vectors of the genus Anopheles in the world belong to the Maculipennis Group, which is subdivided into two Nearctic subgroups (Freeborni and Quadrimaculatus) and one Palearctic (Maculipennis) subgroup. Although previous studies considered the Nearctic subgroups as ancestral, details about their relationship with the Palearctic subgroup, and their migration times and routes from North America to Eurasia remain controversial. The Palearctic species An. beklemishevi is currently included in the Nearctic Quadrimaculatus subgroup adding to the uncertainties in mosquito systematics.

resultsTo reconstruct historic relationships in the Maculipennis Group, we conducted a phylogenomic analysis of 11 Palearctic and 2 Nearctic species based on sequences of 1271 orthologous genes. The analysis indicated that the Palearctic species An. beklemishevi clusters together with other Eurasian species and represents a basal lineage among them. Also, An. beklemishevi is related more closely to An. freeborni, which inhabits the Western United States, rather than to An. quadrimaculatus, a species from the Eastern United States. The time-calibrated tree suggests a migration of mosquitoes in the Maculipennis Group from North America to Eurasia about 20-25 million years ago through the Bering Land Bridge. A Hybridcheck analysis demonstrated highly significant signatures of introgression events between allopatric species An. labranchiae and An. beklemishevi. The analysis also identified ancestral introgression events between An. sacharovi and its Nearctic relative An. freeborni despite their current geographic isolation. The reconstructed phylogeny suggests that vector competence and the ability to enter complete diapause during winter evolved independently in different lineages of the Maculipennis Group.

conclusionsOur phylogenomic analyses reveal migration routes and adaptive radiation timing of Holarctic malaria vectors and strongly support the inclusion of An. beklemishevi into the Maculipennis Subgroup. Detailed knowledge of the evolutionary history of the Maculipennis Subgroup provides a framework for examining the genomic changes related to ecological adaptation and susceptibility to human pathogens. These genomic variations may inform researchers about similar changes in the future providing insights into the patterns of disease transmission in Eurasia.

Indexed as

AnophelesMalariaAnimalsHumansMosquito VectorsPhylogenyAnophelesChromosomesIntrogressionMaculipennis SubgroupMalaria vectorsMigrationMosquitoesPhylogenomicsSpecies radiation

Identifiers

PMID37032389
PMCPMC10084679
OpenAlexW4362731297

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.