Biology subjects

Larsen, T. J.

Publications and source records attributed to Larsen, T. J..

3 recordsLinked to original sources

bioRxiv2026

A history of symbiosis impacts the host evolutionary trajectory in experimentally evolved amoebas

Biological diversity driven by endosymbiosis arises from the intertwined evolution of microbes and their hosts. Each partner affects the fitness and therefore the evolution of the other. Here, we tested a further question: does the history of symbiosis affect evolution even after the partnership is dissolved? We analyzed phenotypic data from experimentally evolved strains of Dictyostelium discoideum hosts, each of which had had its symbiont removed, to study how their traits evolved. We found that host trait evolution was affected by the prior history of infection, specifically by which of three Paraburkolderia bacterial symbionts had been removed. Thus, symbionts affect not only current evolution but also generate path dependence that affects the subsequent evolutionary trajectories even after the symbionts are lost. Impact statementThe evolution of partner dependence in host-microbial symbioses has fundamentally shaped biological diversity and ecosystem function. To examine variation in symbiont dependence in the social amoeba, we compared how different strains of Dictyostelium discoideum respond evolutionarily after the loss of their bacterial symbionts. We analyzed phenotypic data from experimentally evolved strains and found that the absence of different symbiont species leads to distinct changes in the subsequent evolution of key traits like cell proliferation, slug migration, and spore production. This research expands our current understanding of microbial symbiosis by revealing that symbiont species may impact the evolution of their hosts even after the symbiont is gone. Data summaryWe used phenotypic traits data from our previous experimental-evolution dataset from the open-access repository Dryad (https://doi.org/10.5061/dryad.kkwh70s97). Scripts for the statistical analyses are available in a GitHub repository (https://github.com/jahanisrat/SymbiontLoss). The accompanying R project includes code to reproduce the graphs in the results section.

evolutionary biology↗

bioRxiv2023

Symbiotic bacteria, immune-like sentinel cells, and the response to pathogens in a social amoeba

Some endosymbionts living within a host must modulate their hosts immune systems in order to infect and persist. We studied the effect of a bacterial endosymbiont on a facultatively multicellular social amoeba host. Aggregates of the amoeba Dictyostelium discoideum contain a subpopulation of sentinel cells that function akin to the immune systems of more conventional multicellular organisms. Sentinel cells sequester and discard toxins from D. discoideum aggregates and may play a central role in defense against pathogens. We measured the number and functionality of sentinel cells in aggregates of D. discoideum infected by bacterial endosymbionts in the genus Paraburkholderia. Infected D. discoideum produced fewer and less functional sentinel cells, suggesting that Paraburkholderia may interfere with its hosts immune system. Despite impaired sentinel cells, however, infected D. discoideum were less sensitive to ethidium bromide toxicity, suggesting that Paraburkholderia may also have a protective effect on its host. By contrast, D. discoideum infected by Paraburkholderia did not show differences in their sensitivity to two non-symbiotic pathogens. Our results expand previous work on yet another aspect of the complicated relationship between D. discoideum and Paraburkholderia, which has considerable potential as a model for the study of symbiosis.

ecology↗

bioRxiv2018

Proteomics-based comparative mapping of the human brown and white adipocyte secretome reveals EPDR1 as a novel batokine

Secreted proteins from adipose tissue play a role in metabolic cross-talk and homeostasis. We performed high sensitivity mass spectrometry-based proteomics on the cell media of in vitro differentiated, non-immortalized brown adipocytes derived from supraclavicular adipose of adult humans and white adipocytes derived from subcutaneous adipose of adult humans. We identified 471 potentially secreted proteins covering interesting protein categories such as hormones, growth factors, growth factor binding proteins, cytokines, extracellular matrix proteins, and proteins of the complement system, which were differentially regulated in brown and white adipocytes. A total of 101 proteins were exclusively quantified in brown adipocytes, among these ependymin-related protein 1 (EPDR1). Ablation of EPDR1 impaired the induction of thermogenic transcripts in response to norepinephrine in brown adipocytes, while EPDR1-treated mice increased their energy consumption, suggesting a role in brown fat commitment and activation. Our work reveals substantial differences between the secretomes of brown and white human adipocytes and identifies novel candidate batokines.

physiology↗