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Joachim Kurtz

Publications and source records attributed to Joachim Kurtz.

9 recordsLinked to original sources
PubMed2025

Experimental evolution of a pathogen confronted with innate immune memory increases variation in virulence.

Understanding the drivers and mechanisms of virulence evolution is still a major goal of evolutionary biologists and epidemiologists. Theory predicts that the way virulence evolves depends on the balance between the benefits and costs it provides to pathogen fitness. Additionally, host responses to infections, such as resistance or tolerance, play a critical role in shaping virulence evolution. But, while the evolution of pathogens has been traditionally studied under the selection pressure of host adaptive immunity, less is known about their evolution when confronted to simpler and less effective forms of immunity such as immune priming. In this study, we used a well-established insect model for immune priming - red flour beetles and their bacterial pathogen Bacillus thuringiensis tenebrionis - to test how this form of innate immune memory drives the pathogen evolution. Through controlled experimental evolution of the pathogen in primed versus non-primed hosts, we found no change in average virulence after eight selection cycles in primed host. Nonetheless, we observed a notable rise in the variability of virulence, defined as the ability to kill hosts, among independent pathogen lines that evolved in primed hosts, and the bacteria were unable to develop resistance to host priming. Whole genome sequencing revealed increased activity in the bacterial mobilome (prophages and plasmids). Expression of the Cry toxin - a well-known virulence factor - was linked to evolved differences in copy number variation of the cry-carrying plasmid, though this did not correlate directly with virulence. These findings highlight that innate immune memory can drive variability in pathogen traits, which may favor adaptation to variable environments. This underscores the need to consider pathogen evolution in response to innate immune memory when applying these mechanisms in medicine, aquaculture, pest control, and insect mass production.

Animals↗
PubMed2025

Multiomics Reveal Associations Between CpG Methylation, Histone Modifications and Transcription in a Species That has Lost DNMT3, the Colorado Potato Beetle.

Insects display exceptional phenotypic plasticity, which can be mediated by epigenetic modifications, including CpG methylation and histone modifications. In vertebrates, both are interlinked and CpG methylation is associated with gene repression. However, little is known about these regulatory systems in invertebrates, where CpG methylation is mainly restricted to gene bodies of transcriptionally active genes. A widely conserved mechanism involves the co-transcriptional deposition of H3K36 trimethylation and the targeted methylation of unmethylated CpGs by the de novo DNA methyltransferase DNMT3. However, DNMT3 has been lost multiple times in invertebrate lineages raising the question of how the links between CpG methylation, histone modifications and gene expression are affected by its loss. Here, we report the epigenetic landscape of Leptinotarsa decemlineata, a beetle species that has lost DNMT3 but retained CpG methylation. We combine RNA-seq, enzymatic methyl-seq and CUT&Tag to study gene expression, CpG methylation and patterns of H3K36me3 and H3K27ac histone modifications on a genome-wide scale. Despite the loss of DNMT3, H3K36me3 mirrors CpG methylation patterns. Together, they give rise to signature profiles for expressed and not expressed genes. H3K27ac patterns show a prominent peak at the transcription start site that is predictive of expressed genes irrespective of their methylation status. Our study provides new insights into the evolutionary flexibility of epigenetic modification systems that urge caution when generalizing across species.

Animals↗
PubMed2004

Major histocompatibility complex diversity influences parasite resistance and innate immunity in sticklebacks.

Proteins of the major histocompatibility complex (MHC) play a central role in the presentation of antigens to the adaptive immune system. The MHC also influences the odour-based choice of mates in humans and several animal taxa. It has recently been shown that female three-spined sticklebacks (Gasterosteus aculeatus) aim at a moderately high MHC diversity in their offspring when choosing a mate. Do they optimize the immune systems of their offspring? Using three-spined sticklebacks that varied in their individual numbers of MHC class IIB molecules, we tested, experimentally, whether allelic diversity at the MHC influences parasite resistance and immune parameters. We found that sticklebacks with low MHC diversity suffered more from parasite infection after experimental exposure to Schistocephalus solidus tapeworms and Glugea anomala microsporidians. They also showed the highest proportion of granulocytes and the strongest respiratory burst reaction, which are correlates of innate immunity. This indicates a strong activity of the innate immune system after challenge by parasites when MHC diversity is suboptimal. Individuals with very high allelic diversity at the MHC seemed inferior to those with moderately high diversity. Such a pattern is consistent with theoretical expectations of an optimal balance between the number of recognizable antigens and self-tolerance.

Alleles↗
PubMed2003

Innate defence: evidence for memory in invertebrate immunity.

Acquired immunity in vertebrates is characterized by immunological memory and specificity, whereas the innate defence systems of invertebrates are assumed to have no specific memory. Here we use a model system of a copepod, which is a minute crustacean, and a parasitic tapeworm to show that the success of reinfection depends on the antigenic resemblance between the consecutively encountered parasites. This finding indicates that an invertebrate defence system may be capable of specific memory.

Animals↗
PubMed2002

Phagocytosis by invertebrate hemocytes: causes of individual variation in Panorpa vulgaris scorpionflies.

An in vitro phagocytosis assay, adjusted to as little as 1 microL of insect hemolymph, enables the microscopic determination of phagocytosis for single individuals of small insects. Even repeated determination over the lifetime of individuals is possible. This method makes it feasible to study individual variation in invertebrate phagocytic capacity. Possible sources of such variation are reviewed in this article: genetic differences, development, aging, reproduction, presence of parasites, and diverse environmental influences are natural sources of individual variation in phagocytosis. However, the methods used for phagocytosis and microscopic evaluation are also (unwelcome) sources of variation. To optimize incubation time for in vitro phagocytosis, time courses were determined. Furthermore, the reliability of visual counting and image analysis for the microscopic quantification of phagocytosis are compared. The influences of larval development and adult aging on phagocytosis by Panorpa vulgaris hemocytes are subsequently demonstrated. During development, a decrease in hemocyte numbers but a simultaneous increase in the proportion of phagocytosing hemocytes was observed when larvae reached pupation. On the other hand, adults showed a dramatic decrease in phagocytic capacity with age, while cell numbers remained fairly constant. The results show that individual variation in phagocytosis can be determined accurately in small invertebrates and related to its causes. This might be especially interesting in the context of studies relating individual immunocompetence to ecology, life history variation, and behavior.

Aging↗
PubMed2002

Fluorescent vital labeling to track cestodes in a copepod intermediate host.

In experimental studies of host-parasite interactions, it is often important to track parasites in their hosts and to discriminate between individual parasites. We used the fluorescent tracer dyes 7-amino-4-chloromethylcoumarin (CMAC) and, 5-chloromethylfluorescein diacetate (CMFDA) for vital labeling of Schistocephalus solidus (Cestoda) coracidia larvae. Labeling was fast and easy to perform and enabled microscopic detection of parasites appearing as procercoids in the hemocoel of the copepod intermediate host at 3 h after exposure. The label was still visible after 14 days. Extensive controls showed that CMAC (20 microM) labeling did not harm tapeworms or copepods. CMFDA (2 microM) reduced host survival, but the dye concentration can be decreased to avoid this in future studies. The new labeling method presented here has been very useful to track S. solidus parasites. It can be valuable for other parasites also and may be particularly suitable for visualization of individual live macroparasites in invertebrate hosts, for which we are not aware of any other appropriate method.

Animals↗
PubMed2002

Outcrossing increases infection success and competitive ability: experimental evidence from a hermaphrodite parasite.

The maintenance of two genetically distinct reproductive modes such as outcrossing and selfing within a population of animals or plants is still a matter of considerable debate. Hermaphroditic parasites often reproduce either alone by selfing or in pairs by outcrossing. They can be used as a model to study potential benefits of outcrossing. Any advantage from outcrossing may be important, especially in host-parasite coevolution, but has not, to our knowledge, been studied yet in any parasite species. We studied the potential effect of outcrossing in a tapeworm, Schistocephalus solidus, on both infection success and growth in its first intermediate host, the copepod Macrocyclops albidus. Tapeworms that had been obtained from natural populations of three-spined sticklebacks (Gasterosteus aculeatus) were allowed to reproduce either alone or in pairs, in an in vitro system that replaced the final host's gut. This resulted in either selfed or outcrossed offspring, respectively. In one part of the experiment, copepods were exposed to either selfed or outcrossed parasites, in a second part to both types simultaneously, in order to study the effect of competition between them. To discriminate parasites of either origin within the same host, a novel method for fluorescent vital labeling was used. We show here for the first time that outcrossed parasites had a higher infection success and faster development in the host. This advantage of outcrossing became apparent only in the competitive situation, in which superior abilities of parasites to extract limiting resources from the host become crucial.

Animals↗
PubMedDate not supplied

Evaluation of an innate immune reaction to parasites in earthworms.

Encapsulation is an essential process of the invertebrate immune system and includes the prophenoloxidase (proPO) cascade. We present an assay for evaluating this immune response, now newly adapted to earthworms. Coelomic fluid is withdrawn and coelomocytes are stained with l-Dopa. We studied assay repeatability and the correlation between number of PO-active cells and infection level of the parasitic protozoan Monocystis sp. in the earthworm Lumbricus terrestris. Our study showed high assay repeatability although the expected negative relationship between PO-active coelomocytes and parasite load was not observed; yet a suggestion toward a positive relationship was detected. This finding is contrary to previous assumptions that presume coelomocyte concentrations to be the independent variable determining parasite load.

Animals↗