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Is host specificity the cause or the consequence
           of parasite diversification:
   lessons from the population genetics of lice and
                     helminths

                            Štefka, Jan1,2



1Natural History Museum, Cromwell Road, London, UK
2Faculty of Science, University of South Bohemia and Biology Centre ASCR,

 České Budějovice, CZ
Evolution of novel taxa in parasites:
host specificity vs. geografic distribution.
 •   Host specificity and speciation in metazoan parasites
      – What is host specificity
      – Why bother
      – Established framework?
 •   Timescale: long vs. short evolutionary periods
Timescale: long vs. short evolutionary periods




 Estimate the amount of co-speciations vs. host switches
Evolution of novel taxa in parasites:
host specificity vs. geografic distribution.
 •   Speciation and host specificity

 •   Timescale: long vs. short evolutionary periods

 •   Careful choise of model taxa (complexity of life-cycles and
     population histories…)
The importance of geography




                              Štefka et al, in prep.
traditional taxonomy
mtDNA phylogeny




                                  N. parvulus



                                                   N. melanotis




                       N. trifasciatus          N. macdonaldi
traditional taxonomy
mtDNA phylogeny




                                  N. parvulus



                                                   N. melanotis




                       N. trifasciatus          N. macdonaldi
Myrsidea sp.
98 specimens, 37 haps



                 N. trifasciatus




                 N. parvulus


                            N. trifasciatus
            N. melanotis


          N. macdonaldi
Analges sp. (Acari, Astigmata)
87 specimens, 71 haps




           N. parvulus




                                 N. trifasciatus


                   N. melanotis


                  N. macdonaldi
7.000 YA

           approx. 2-3 MYA




                             approx. 5 MYA
                                             5-9 MYA
7.000 YA

           approx. 2-3 MYA




                             approx. 5 MYA
                                             5-9 MYA



           Progression rule
Polyplax serrata




                   genus Apodemus
Michaux et al., 2003, 2005




                               ?
A. sylvaticus
                     A. flavicollis
northern border of A. sylvaticus range
A. sylvaticus   A. flavicollis        A. agrarius           A. uralensis
A
                             A. flavicollis
                             A. sylvaticus


                                     colonization
COI                                      vs.
Haplotypes       B                  duplication ?
+
EF1α
                           A. flavicollis


             C       A. agrarius
                     A. uralensis
                                      Štefka and Hypša, 2008
                                      Martinů et al, in prep.
A


                   colonization


B
            molecular dating
            -Clade A/B 1.5 Mya (1.4-1.6)
            -Hosts Af/As 4 Mya


    A


                   duplication

    B   Host specificity arose in allopatry
Ligula intestinalis s.l.
A
                                                Tunisia




Sympatric lineages,
different host. spec.
                                                           B
Mutual def. hosts                                         Tunisia

 COI+COB
 haplotypes




       Bouzid et al, 2008, Int. J. Parasitol.
       Bouzid et al, in prep.
Structure 2.2; 338 tapeworms
               Europe Europe/Gobio TunisiaAlgeria/Barbus
                             X




Compatible with mtDNA                    Lake Tana
                                         (Ethiopia)




                                 B. humilis           B. tsanensis
                                                      B. intermedius
                                                      B. brevicephalus


                                                Štefka et al., 2009, Mol. Ecol.
Conclusions


•    Host specificity arose in allopatry in P. serrata

•    More complex picture in L. intestinalis: some lineages arising in
     allopatry vs. ongoing host-dependant speciation in others.

•    Host specificity is at least in some cases a product of speciation
     processes not the motor of speciation in parasites.
Václav Hypša
Thanks to:                                              Faculty of Science, USB, Č. Budějovice
                                                        Czech Rep.




             Jana Martinů
  Faculty of Science, USB, Č. Budějovice                                 Vince Smith
                 Czech Rep.                                       Entomology Dept., NHM, London
                                                                               UK

                                       Wafa Bouzid
                               Université P. Sebatier, Toulouse
                                            France



Acknowledgements:
This work was supported by Grant Agency of the Czech Republic (project
No. 206/08/1019) and by Marie Curie Fellowship (project Galápagos, no.
235123, FP7-PEOPLE-IEF-2008).

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Host Specificity and Parasite Diversification

  • 1. Is host specificity the cause or the consequence of parasite diversification: lessons from the population genetics of lice and helminths Štefka, Jan1,2 1Natural History Museum, Cromwell Road, London, UK 2Faculty of Science, University of South Bohemia and Biology Centre ASCR, České Budějovice, CZ
  • 2. Evolution of novel taxa in parasites: host specificity vs. geografic distribution. • Host specificity and speciation in metazoan parasites – What is host specificity – Why bother – Established framework? • Timescale: long vs. short evolutionary periods
  • 3. Timescale: long vs. short evolutionary periods Estimate the amount of co-speciations vs. host switches
  • 4. Evolution of novel taxa in parasites: host specificity vs. geografic distribution. • Speciation and host specificity • Timescale: long vs. short evolutionary periods • Careful choise of model taxa (complexity of life-cycles and population histories…)
  • 5. The importance of geography Štefka et al, in prep.
  • 6. traditional taxonomy mtDNA phylogeny N. parvulus N. melanotis N. trifasciatus N. macdonaldi
  • 7. traditional taxonomy mtDNA phylogeny N. parvulus N. melanotis N. trifasciatus N. macdonaldi
  • 8. Myrsidea sp. 98 specimens, 37 haps N. trifasciatus N. parvulus N. trifasciatus N. melanotis N. macdonaldi
  • 9. Analges sp. (Acari, Astigmata) 87 specimens, 71 haps N. parvulus N. trifasciatus N. melanotis N. macdonaldi
  • 10. 7.000 YA approx. 2-3 MYA approx. 5 MYA 5-9 MYA
  • 11. 7.000 YA approx. 2-3 MYA approx. 5 MYA 5-9 MYA Progression rule
  • 12. Polyplax serrata genus Apodemus
  • 13. Michaux et al., 2003, 2005 ? A. sylvaticus A. flavicollis
  • 14. northern border of A. sylvaticus range A. sylvaticus A. flavicollis A. agrarius A. uralensis
  • 15. A A. flavicollis A. sylvaticus colonization COI vs. Haplotypes B duplication ? + EF1α A. flavicollis C A. agrarius A. uralensis Štefka and Hypša, 2008 Martinů et al, in prep.
  • 16. A colonization B molecular dating -Clade A/B 1.5 Mya (1.4-1.6) -Hosts Af/As 4 Mya A duplication B Host specificity arose in allopatry
  • 18.
  • 19. A Tunisia Sympatric lineages, different host. spec. B Mutual def. hosts Tunisia COI+COB haplotypes Bouzid et al, 2008, Int. J. Parasitol. Bouzid et al, in prep.
  • 20. Structure 2.2; 338 tapeworms Europe Europe/Gobio TunisiaAlgeria/Barbus X Compatible with mtDNA Lake Tana (Ethiopia) B. humilis B. tsanensis B. intermedius B. brevicephalus Štefka et al., 2009, Mol. Ecol.
  • 21. Conclusions • Host specificity arose in allopatry in P. serrata • More complex picture in L. intestinalis: some lineages arising in allopatry vs. ongoing host-dependant speciation in others. • Host specificity is at least in some cases a product of speciation processes not the motor of speciation in parasites.
  • 22. Václav Hypša Thanks to: Faculty of Science, USB, Č. Budějovice Czech Rep. Jana Martinů Faculty of Science, USB, Č. Budějovice Vince Smith Czech Rep. Entomology Dept., NHM, London UK Wafa Bouzid Université P. Sebatier, Toulouse France Acknowledgements: This work was supported by Grant Agency of the Czech Republic (project No. 206/08/1019) and by Marie Curie Fellowship (project Galápagos, no. 235123, FP7-PEOPLE-IEF-2008).