Showing 21 - 30 of 116 Items

Date: 2025-01-01
Creator: Aeri Ko
Access: Access restricted to the Bowdoin Community
Date: 2014-12-01
Creator: Anja Wartenberg, Jörg Linde, Ronny Martin, Maria Schreiner, Fabian, Horn, Ilse D. Jacobsen, Sabrina Jenull, Thomas Wolf, Karl Kuchler, Reinhard Guthke, Oliver Kurzai, Anja Forche, Christophe d'Enfert, Sascha Brunke, Bernhard Hube
Access: Open access
- Following antifungal treatment, Candida albicans, and other human pathogenic fungi can undergo microevolution, which leads to the emergence of drug resistance. However, the capacity for microevolutionary adaptation of fungi goes beyond the development of resistance against antifungals. Here we used an experimental microevolution approach to show that one of the central pathogenicity mechanisms of C. albicans, the yeast-to-hyphae transition, can be subject to experimental evolution. The C. albicans cph1Δ/efg1Δ mutant is nonfilamentous, as central signaling pathways linking environmental cues to hyphal formation are disrupted. We subjected this mutant to constant selection pressure in the hostile environment of the macrophage phagosome. In a comparatively short time-frame, the mutant evolved the ability to escape macrophages by filamentation. In addition, the evolved mutant exhibited hyper-virulence in a murine infection model and an altered cell wall composition compared to the cph1Δ/efg1Δ strain. Moreover, the transcriptional regulation of hyphae-associated, and other pathogenicity-related genes became re-responsive to environmental cues in the evolved strain. We went on to identify the causative missense mutation via whole genome- and transcriptome-sequencing: a single nucleotide exchange took place within SSN3 that encodes a component of the Cdk8 module of the Mediator complex, which links transcription factors with the general transcription machinery. This mutation was responsible for the reconnection of the hyphal growth program with environmental signals in the evolved strain and was sufficient to bypass Efg1/Cph1-dependent filamentation. These data demonstrate that even central transcriptional networks can be remodeled very quickly under appropriate selection pressure.

- Restriction End Date: 2025-06-01
Date: 2020-01-01
Creator: Rhianna J Patel
Access: Access restricted to the Bowdoin Community
Date: 2024-01-01
Creator: Karin van Hassel
Access: Open access
- The cardiac ganglion (CG) is a central pattern generator, a neural network that, when activated, produces patterned motor outputs such as breathing and walking. The CG induces the heart contractions of the American lobster, Homarus americanus, making the lobster heart neurogenic. In the American lobster, the CG is made up of nine neurons: four premotor pacemaker neurons that send signals to five motor neurons, causing bursts of action potentials from the motor neurons. These bursts cause cardiac muscle contractions that vary in strength based on the burst duration, frequency, and pattern. The activity of the CG is modulated by feedback pathways and neuromodulators, allowing for flexibility in the CG’s motor output and appropriate responses to changes in the animal’s environment. Two feedback pathways modulate the CG motor output, the excitatory cardiac muscle stretch and inhibitory nitric oxide feedback pathways. Despite our knowledge of the modulation of the CG by feedback pathways and neuromodulators separately, little is known about how neuromodulators influence the sensory feedback response to cardiac muscle stretch. I found one neuromodulator to modulate each phase of the stretch response differently, one neuromodulator to generally not affect the stretch response, and three neuromodulators to suppress the stretch response. These results suggest neuromodulators can act to produce flexibility in a CPG’s motor output, allowing the system to respond appropriately to changes in an organism’s environment, and allow for variation in CPG responses to different stimuli.
Date: 2023-01-01
Creator: Jackie Seddon
Access: Open access
- Neuromodulation, the process of altering the electrical outputs of a neuron or neural circuit, allows an organism to control its physiological processes to meet the needs of both its internal and external environments. Previous work shows that the pyloric pattern of the kelp crab (Pugettia producta) stomatogastric nervous system (STNS) neurons responded to fewer neuromodulators than the Jonah crab (Cancer borealis). Since the kelp crab diet primarily eats kelp, it is possible that the movements of the foregut that control digestion may require less flexibility in functional output compared to an opportunistic feeder. To determine whether a reduced flexibility is correlated with diet, this study compared the modulatory responses in Pugettia to two other species of majoid crabs: Chionoecetes opilio and Libinia emarginata, which are both opportunistic feeders. Pooled data for this study found that Libinia and Chionoecetes responded to all twelve modulators tested. When considering the effect of modulators on stomatogastric ganglion (STG) motor outputs, we must consider whether these modulators also alter the excitatory junction potentials (EJPs) at the neuromuscular junction (NMJ), and whether there are differences in responses across species. To test this, the dorsal gastric nerve (dgn) was stimulated while recording intracellularly from the muscle fibers of the associated gm4 muscles. The NMJ of the gm4 in Cancer borealis did not appear to be broadly modulated, as only RPCH and CabTRP showed increases in amplitude, and RPCH decreased facilitation at 5 Hz.

- Embargo End Date: 2026-05-18
Date: 2023-01-01
Creator: Violet Louise Rizzieri
Access: Embargoed

Date: 2024-01-01
Creator: Nuanxi (Sissi) Feng
Access: Access restricted to the Bowdoin Community

Date: 2016-05-01
Creator: Tess Lameyer
Access: Access restricted to the Bowdoin Community

Date: 2025-01-01
Creator: Emma F.B. Gibbens
Access: Access restricted to the Bowdoin Community
Date: 2010-07-01
Creator: Anna Selmecki, Anja Forche, Judith Berman
Access: Open access
- The genomic plasticity of Candida albicans, a commensal and common opportunistic fungal pathogen, continues to reveal unexpected surprises. Once thought to be asexual, we now know that the organism can generate genetic diversity through several mechanisms, including mating between cells of the opposite or of the same mating type and by a parasexual reduction in chromosome number that can be accompanied by recombination events (2, 12, 14, 53, 77, 115). In addition, dramatic genome changes can appear quite rapidly in mitotic cells propagated in vitro as well as in vivo. The detection of aneuploidy in other fungal pathogens isolated directly from patients (145) and from environmental samples (71) suggests that variations in chromosome organization and copy number are a common mechanism used by pathogenic fungi to rapidly generate diversity in response to stressful growth conditions, including, but not limited to, antifungal drug exposure. Since cancer cells often become polyploid and/or aneuploid, some of the lessons learned from studies of genome plasticity in C. albicans may provide important insights into how these processes occur in higher-eukaryotic cells exposed to stresses such as anticancer drugs. © 2010, American Society for Microbiology.