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1.
PLoS Biol ; 13(6): e1002169, 2015 Jun.
Article in English | MEDLINE | ID: mdl-26042786

ABSTRACT

Reciprocal coevolution between host and pathogen is widely seen as a major driver of evolution and biological innovation. Yet, to date, the underlying genetic mechanisms and associated trait functions that are unique to rapid coevolutionary change are generally unknown. We here combined experimental evolution of the bacterial biocontrol agent Bacillus thuringiensis and its nematode host Caenorhabditis elegans with large-scale phenotyping, whole genome analysis, and functional genetics to demonstrate the selective benefit of pathogen virulence and the underlying toxin genes during the adaptation process. We show that: (i) high virulence was specifically favoured during pathogen-host coevolution rather than pathogen one-sided adaptation to a nonchanging host or to an environment without host; (ii) the pathogen genotype BT-679 with known nematocidal toxin genes and high virulence specifically swept to fixation in all of the independent replicate populations under coevolution but only some under one-sided adaptation; (iii) high virulence in the BT-679-dominated populations correlated with elevated copy numbers of the plasmid containing the nematocidal toxin genes; (iv) loss of virulence in a toxin-plasmid lacking BT-679 isolate was reconstituted by genetic reintroduction or external addition of the toxins. We conclude that sustained coevolution is distinct from unidirectional selection in shaping the pathogen's genome and life history characteristics. To our knowledge, this study is the first to characterize the pathogen genes involved in coevolutionary adaptation in an animal host-pathogen interaction system.


Subject(s)
Bacillus thuringiensis/genetics , Bacterial Proteins/genetics , Biological Evolution , Host-Pathogen Interactions/genetics , Receptors, Cell Surface/genetics , Selection, Genetic , Animals , Bacillus thuringiensis/pathogenicity , Caenorhabditis elegans/microbiology , Genome, Bacterial , Genomics , Genotype , Insect Proteins , Phenotype , Virulence
2.
PLoS One ; 6(9): e24619, 2011.
Article in English | MEDLINE | ID: mdl-21931778

ABSTRACT

Pathogens represent a universal threat to other living organisms. Most organisms express antimicrobial proteins and peptides, such as lysozymes, as a protection against these challenges. The nematode Caenorhabditis elegans harbours 15 phylogenetically diverse lysozyme genes, belonging to two distinct types, the protist- or Entamoeba-type (lys genes) and the invertebrate-type (ilys genes) lysozymes. In the present study we characterized the role of several protist-type lysozyme genes in defence against a nematocidal strain of the Gram-positive bacterium Bacillus thuringiensis. Based on microarray and subsequent qRT-PCR gene expression analysis, we identified protist-type lysozyme genes as one of the differentially transcribed gene classes after infection. A functional genetic analysis was performed for three of these genes, each belonging to a distinct evolutionary lineage within the protist-type lysozymes (lys-2, lys-5, and lys-7). Their knock-out led to decreased pathogen resistance in all three cases, while an increase in resistance was observed when two out of three tested genes were overexpressed in transgenic lines (lys-5, lys-7, but not lys-2). We conclude that the lysozyme genes lys-5, lys-7, and possibly lys-2 contribute to resistance against B. thuringiensis, thus highlighting the particular role of lysozymes in the nematode's defence against pathogens.


Subject(s)
Bacillus thuringiensis/pathogenicity , Caenorhabditis elegans Proteins/metabolism , Caenorhabditis elegans/metabolism , Caenorhabditis elegans/microbiology , Muramidase/metabolism , Animals , Caenorhabditis elegans Proteins/genetics , Muramidase/genetics
3.
Proc Biol Sci ; 271(1543): 1001-7, 2004 May 22.
Article in English | MEDLINE | ID: mdl-15293852

ABSTRACT

Asexual populations are usually considered evolutionary dead-ends because they lack the mechanisms to generate and maintain sufficient genetic diversity. Yet, some asexual forms are remarkably widespread and genetically diverse. This raises the question whether asexual systems are always truly clonal or whether they have cryptic forms of sexuality that enhance their viability. In the planarian flatworm Schmidtea polychroa parthenogens are functional hermaphrodites (as are their sexual conspecifics), copulate and exchange sperm. Sperm is required for initiation of embryogenesis but usually does not contribute genetically to the offspring (sperm-dependent parthenogenesis). Using karyology and genotyping of parents and offspring, we show that in a purely parthenogenetic population an estimated 12% of all offspring are the result of partial genetic exchange. Several processes of chromosome addition and loss are involved. Some of these result in an alternation between a common triploid and a rare tetraploid state. We conclude that genetic recombination does not necessarily require segregation and fusion within the same generation, as is the case in most sexual species. These occasional sexual processes help to explain the geographical dominance of parthenogens in our study species.


Subject(s)
Chromosomes/genetics , Disorders of Sex Development , Models, Biological , Parthenogenesis/physiology , Planarians/physiology , Sexual Behavior, Animal/physiology , Animals , DNA Primers , Fresh Water , Gene Frequency , Genotype , Germany , Karyotyping , Male , Microsatellite Repeats/genetics , Polyploidy , Recombination, Genetic/genetics , Sequence Analysis, DNA , Spermatozoa/physiology
4.
Mol Ecol ; 13(7): 2101-6, 2004 Jul.
Article in English | MEDLINE | ID: mdl-15189230

ABSTRACT

Abstract Microsatellites are powerful molecular markers, used commonly to estimate intraspecific genetic distances. With the exception of band sharing similarity index, available distance measures were developed specifically for diploid organisms and are unsuited for comparisons of polyploids. Here, we present a simple method for calculation of microsatellite genotype distances, which takes into account mutation processes and permits comparison of individuals with different ploidy levels. This method should provide a valuable tool for intraspecific analyses of polyploid organisms, which are widespread among plants and some animal taxa. An illustration is given using data from the planarian flatworm Schmidtea polychroa (Platyhelminthes).


Subject(s)
Evolution, Molecular , Genetic Variation , Microsatellite Repeats/genetics , Models, Genetic , Ploidies , Animals , DNA Primers , Genotype , Italy , Mutation/genetics , Planarians/genetics
5.
BMC Evol Biol ; 3: 23, 2003 Nov 17.
Article in English | MEDLINE | ID: mdl-14622447

ABSTRACT

BACKGROUND: Models of the maintenance of sex predict that one reproductive strategy, sexual or parthenogenetic, should outcompete the other. Distribution patterns may reflect the outcome of this competition as well as the effect of chance and historical events. We review the distribution data of sexual and parthenogenetic biotypes of the planarian Schmidtea polychroa. RESULTS: S. polychroa lives in allopatry or sympatry across Europe except for Central and North-Western Europe, where sexual individuals have never been reported. A phylogenetic relationship between 36 populations based on a 385 bp fragment of the mitochondrial cytochrome oxidase I gene revealed that haplotypes were often similar over large geographic distances. In North Italian lakes, however, diversity was extreme, with sequence differences of up to 5% within the same lake in both sexuals and parthenogens. Mixed populations showed "endemic" parthenogenetic lineages that presumably originated from coexisting sexuals, and distantly related ones that probably result from colonization by parthenogens independent from sexuals. CONCLUSIONS: Parthenogens originated repeatedly from sexuals, mainly in Italy, but the same may apply to other Mediterranean regions (Spain, Greece). The degree of divergence between populations suggests that S. polychroa survived the ice ages in separate ice-free areas in Central, Eastern and Southern Europe and re-colonised Europe after the retreat of the major glaciers. Combining these results with those based on nuclear markers, the data suggest that repeated hybridisation between sexuals and parthenogenetic lineages in mixed populations maintains high levels of genetic diversity in parthenogens. This can explain why parthenogens persist in populations that were originally sexual. Exclusive parthenogenesis in central and western populations suggests better colonisation capacity, possibly because of inbreeding costs as well as hybridisation of sexuals with parthenogens.


Subject(s)
Hybridization, Genetic , Parthenogenesis , Phylogeny , Planarians/classification , Animals , Biological Evolution , Competitive Behavior , Europe , Fresh Water , Haplotypes , Molecular Sequence Data , Planarians/genetics , Reproduction
6.
Evolution ; 52(1): 109-115, 1998 Feb.
Article in English | MEDLINE | ID: mdl-28568155

ABSTRACT

Parthenogenetic lineages that arise in a hermaphroditic, sexual population will inherit the male function from their sexual progenitors. Natural selection then acts to reduce male allocation of the parthenogens, freeing resources presumably for the female function. Depending on age and the available genetic variation, one therefore expects to find reduced male allocation in naturally occurring parthenogenetic lineages. We investigated the allocation to sperm production in the hermaphroditic flatworm Dugesia polychroa in three lakes containing a sexual (S), a (pseudogamous) parthenogenetic (P), and a mixed sexual-parthenogenetic population (M). Parthenogenetic lineages from M were assumed to be relatively young due to recurrent origins from the coexisting sexuals, whereas those from P were assumed to be older on biogeographical grounds. As predicted, we found drastically reduced sperm production in parthenogens compared to sexuals, even in the parthenogenetic lineages from M, which may be younger. M parthenogens did not have more testes, but produced more sperm than individuals from the purely parthenogenetic population (P). However, the latter result could not be reproduced with laboratory-raised animals and therefore may be a consequence of different ecological conditions in the different lakes, for example, differences in mating rates. To study the behavioral component of male allocation, copulation frequencies were recorded for sexuals from M and for parthenogens from P. Compared to the drastic reduction in sperm production, copulation frequency was less reduced in parthenogens. This may be a consequence of allosperm limitation in pseudogamous parthenogenetic populations.

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