Polyplax praomydis

Bothma, Johannes C, Matthee, Sonja & Matthee, Conrad A, 2021, Comparative phylogeography between parasitic sucking lice and their host the Namaqua rock mouse, Micaelamys namaquensis (Rodentia: Muridae), Zoological Journal of the Linnean Society 192 (3), pp. 1017-1028 : 1023-1024

publication ID

https://doi.org/ 10.1093/zoolinnean/zlaa122

persistent identifier

https://treatment.plazi.org/id/03CB8794-FFB9-034C-6299-F979BE56FD31

treatment provided by

Felipe

scientific name

Polyplax praomydis
status

 

POLYPLAX PRAOMYDIS View in CoL PHYLOGEOGRAPHIC STRUCTURE

The mtDNA TCS network for P. praomydis reveals two haplogroups that could not be connected with 95% confidence ( Fig. 2C View Figure 2 ). All P. praomydis individuals from all nine localities sampled in the central and western parts of the country form part of the same haplogroup (central/SW; Fig. 2C View Figure 2 ). This pattern is consistent to what has been found in the host and for H. patersoni . The second P. praomydis haplogroup (NE 1) only includes individuals from Mogalakwena (MO; Fig. 2C View Figure 2 ) and correspond to the host NE1 clade ( Fig. 2A View Figure 2 ). These two haplogroups are separated by a mtDNA sequence divergence of 14.6% (± 2.3%; 40 mutational steps). Although all P.praomydis individuals could be connected with 95% confidence in the nuDNA TCS network, the two haplogroups (retrieved in the mtDNA data) differ by two mutational steps ( Fig. 3C View Figure 3 ). The TrNef+G model (nst = 6; rates = gamma) of sequence evolution was assigned for the first and third codons, whilst the K81 model (nst = 6; rates = equal) was assigned to the second codon. The concatenated mtDNA and nuDNA analysis reveals significant posterior probability and high bootstrap support for both the monophyly of the NE 1 lineage and the central/SW lineage (Supporting Information, Appendix S1). Analyses of molecular variance support significant differentiation among the haplogroups of P. praomydis with 93.6% (P <0.05) of the mtDNA variation assigned to this category and a further 5.5% (P <0.05) assigned to variation among localities within haplogroups ( Table 2). A similar picture is obtained for the nuclear DNA analyses where 92.9% (P <0.05) of the variation is confined to variation between haplogroups ( Table 2). Polyplax praomydis populations show a near absence of gene flow among sampling sites [mtDNA Фst of 0.99 (P <0.05); nuclear Фst of 0.97 (P <0.05); Table 2]. Significant mtDNA pairwise Фst values also support the differentiation among almost all sampling localities (Supporting Information, Appendix S2). Nonsignificant pairwise Фst values are confined to pairwise comparisons between Tswalu (TS), Postmasburg (PB) and Rooipoort (RP) sampling localities (Supporting Information, Appendix S2).

Co-divergence

CO- PHYLOGENY

All parasite and host individuals belonging to the CSW clade form a strongly supported monophyletic group (96% bootstrap support; 1.00 posterior probability; Supporting Information, Appendix S1). Conflicts between the parasite and host trees are all confined to the four localities found in the NE1 and NE2 clades (Supporting Information, Appendix S1). The JANE co-phylogenetic reconstruction between M. namaquensis and H. patersoni reveals that the most parsimonious solution with a total cost of three, includes three co-divergences, one host switch and one loss ( Fig. 4 View Figure 4 ). Both of the statistical analyses indicated non-significant co-phylogeny between the M. namaquensis and H. patersoni , with P = 0.39 and P = 0.27 for random tip mapping and random parasite tree, respectively.

Kingdom

Animalia

Phylum

Arthropoda

Class

Insecta

Order

Psocodea

Family

Polyplacidae

Genus

Polyplax

Kingdom

Animalia

Phylum

Arthropoda

Class

Insecta

Order

Psocodea

Family

Polyplacidae

Genus

Polyplax

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