» Articles » PMID: 30165810

Integrating Coalescent Species Delimitation with Analysis of Host Specificity Reveals Extensive Cryptic Diversity Despite Minimal Mitochondrial Divergence in the Malaria Parasite Genus Leucocytozoon

Overview
Journal BMC Evol Biol
Publisher Biomed Central
Specialty Biology
Date 2018 Sep 1
PMID 30165810
Citations 19
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Coalescent methods that use multi-locus sequence data are powerful tools for identifying putatively reproductively isolated lineages, though this approach has rarely been used for the study of microbial groups that are likely to harbor many unrecognized species. Among microbial symbionts, integrating genetic species delimitation methods with trait data that could indicate reproductive isolation, such as host specificity data, has rarely been used despite its potential to inform species limits. Here we test the ability of an integrative approach combining genetic and host specificity data to delimit species within the avian malaria parasite genus Leucocytozoon in central Alaska.

Results: We sequenced seven nuclear loci for 69 Leucocytozoon samples and used multiple species delimitation methods (GMYC and BPP models), tested for differences in host infection patterns among putative species based on 406 individual infections, and characterized parasite morphology. We found that cryptic morphology has masked a highly diverse Leucocytozoon assemblage, with most species delimitation methods recovering support for at least 21 separate species that occur sympatrically and have divergent host infection patterns. Reproductive isolation among putative species appears to have evolved despite low mtDNA divergence, and in one instance two Leucocytozoon cytb haplotypes that differed by a single base pair (~ 0.2% divergence) were supported as separate species. However, there was no consistent association between mtDNA divergence and species limits. Among cytb haplotypes that differed by one to three base pairs we observed idiosyncratic patterns of nuclear and ecological divergence, with cytb haplotype pairs found to be either conspecific, reproductively isolated with no divergence in host specificity, or reproductively isolated with divergent patterns of host specialization.

Conclusion: Integrating multi-locus genetic species delimitation methods and non-traditional ecological data types such as host specificity provide a novel view of the diversity of avian malaria parasites that has been missed previously using morphology and mtDNA barcodes. Species delimitation methods show that Leucocytozoon is highly species-rich in Alaska, and the genus is likely to harbor extraordinary species-level diversity worldwide. Integrating genetic and ecological data will be an important approach for understanding the diversity and evolutionary history of microbial symbionts moving forward.

Citing Articles

Leucocytozoon infections in tits (Aves, Paridae): blood and tissue stages investigated using an integrative approach.

Gutierrez-Liberato G, Duc M, Eigirdas V, Chagas C Parasite. 2025; 32:13.

PMID: 39982000 PMC: 11843983. DOI: 10.1051/parasite/2025007.


Migratory birds have a distinct haemosporidian community and are temporally decoupled from vector abundance at a stopover site.

Galen S, Ostrow E, Ray S, Henry M, Dispoto J, Fetterman A Parasitology. 2024; 151(12):1326-1335.

PMID: 39523650 PMC: 11893997. DOI: 10.1017/S0031182024001239.


First microscopic, pathological, epidemiological, and molecular investigation of (Apicomplexa: ) parasites in Egyptian pigeons.

Elshahawy I, Mohammed E, Mawas A, Shibat El Hamd D, Ali E, Alghamdi A Front Vet Sci. 2024; 11:1434627.

PMID: 39170633 PMC: 11335660. DOI: 10.3389/fvets.2024.1434627.


Mitochondrial genome amplification of avian haemosporidian parasites from single-infected wildlife samples using a novel nested PCR approach.

Musa S Parasitol Res. 2023; 122(12):2967-2975.

PMID: 37787788 PMC: 10667411. DOI: 10.1007/s00436-023-07986-1.


Exo-erythrocytic development of parasites (Haemosporida, Leucocytozoidae) in song thrushes .

Chagas C, Duc M, Himmel T, Eigirdas V, Weissenbock H, Valkiunas G Int J Parasitol Parasites Wildl. 2023; 22:60-68.

PMID: 37692054 PMC: 10485597. DOI: 10.1016/j.ijppaw.2023.08.008.


References
1.
Reeves A, Smith M, Meixell B, Fleskes J, Ramey A . Genetic diversity and host specificity varies across three genera of blood parasites in ducks of the Pacific Americas Flyway. PLoS One. 2015; 10(2):e0116661. PMC: 4339737. DOI: 10.1371/journal.pone.0116661. View

2.
Charlesworth B . Fundamental concepts in genetics: effective population size and patterns of molecular evolution and variation. Nat Rev Genet. 2009; 10(3):195-205. DOI: 10.1038/nrg2526. View

3.
Puillandre N, Lambert A, Brouillet S, Achaz G . ABGD, Automatic Barcode Gap Discovery for primary species delimitation. Mol Ecol. 2011; 21(8):1864-77. DOI: 10.1111/j.1365-294X.2011.05239.x. View

4.
Woodford L, Bianco G, Ivanova Y, Dale M, Elmer K, Rae F . Vector species-specific association between natural Wolbachia infections and avian malaria in black fly populations. Sci Rep. 2018; 8(1):4188. PMC: 5843599. DOI: 10.1038/s41598-018-22550-z. View

5.
Blair C, Bryson Jr R . Cryptic diversity and discordance in single-locus species delimitation methods within horned lizards (Phrynosomatidae: Phrynosoma). Mol Ecol Resour. 2017; 17(6):1168-1182. DOI: 10.1111/1755-0998.12658. View