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Carter, B. D.

Publications and source records attributed to Carter, B. D..

2 recordsLinked to original sources

Endospore integrity and viability of Bacillus subtilis on simulated Martian regolith in rotational UVC radiation exposures

Current understanding of Martian regolith has advanced due to various rover explorations. Due to this, there are now several variants of Martian regolith that are chemically known and commercially available. These simulants are vital for panspermia models that suggest a transfer of simple life throughout the solar system via ejecta containing life from Mars when its surface was more favourable to host life. Bacteria that produce endospores are suitable candidates for these models as they have adequate protection from the harsh conditions of space, particularly against solar radiation. To assess this, the simple endospore former, Bacillus subtilis, was assessed for growth on several Martian regolith that represented different locations and epochs of Mars. This consisted of a conventional Martian regolith, a sulphur rich regolith, and a simulant of the Jezero crater which was thought to have once been flooded with water. We found that the sulphur rich regolith inhibited endospore formation, while the other two variants favoured endospore production. Interestingly, we also identified that pulsing of UVC in a simulation of endospores on rotational ejecta show that endospores break down faster with lower rotational frequency despite receiving the same UVC dose. Moreover, and most strikingly is that viable endospores after surviving UVC dosage displayed elevated expression of the DNA damage SOS response gene, RecA. Importantly, this study suggests that astrobiological approaches that utilise endospore viability as a benchmark for survival require reassessment as genomic integrity may be compromised. ImportanceCurrent panspermia models that explore the potential interplanetary transfer of simple microbes, particularly those that focus on Mars, apply a combination of Martian topology and bacterial survival. This study assesses Bacillus subtilis endospore formation on different Martain regolith mediums and simulates their potential exposure on fast and slow rotations while being exposed to UV radiation to simulate space radiation. We outline what regions of Mars would be suitable for the formation of endospores, and moreover, we assess viable endospores post-exposure for the expression of the SOS DNA damage repair gene, RecA. Endospores that are viable after withstanding near lethal doses of UVC show elevated expression of RecA. While our study adds vital information to understanding Martian topography and microbial survival, our finding RecA expression analysis post-exposure adds important information to our understanding of endospores as a whole and should be factored into future astrobiological approaches.

microbiology↗

Jedi-1/MEGF12-mediated phagocytosis controls the pro-neurogenic properties of microglia in the ventricular-subventricular zone

Microglia are the primary phagocytes in the central nervous system and are responsible for clearing dead cells generated during development or disease. The phagocytic process shapes the phenotype of the microglia, which affects the local environment. A unique population of microglia reside in the ventricular-subventricular zone (V-SVZ) of neonatal mice, but how they influence this neurogenic niche is not well-understood. Here, we demonstrate that phagocytosis creates a pro-neurogenic microglial phenotype in the V-SVZ and that these microglia phagocytose apoptotic cells via the engulfment receptor Jedi-1. Deletion of Jedi-1 decreases apoptotic cell clearance, triggering the development of a neuroinflammatory phenotype, reminiscent of neurodegenerative and-age-associated microglia, that reduces neural precursor proliferation via elevated interleukin (IL)-1{beta} signaling; inhibition of IL-1 receptor rescues precursor proliferation in vivo. Together, these results reveal a critical role for Jedi-1 in connecting microglial phagocytic activity to a phenotype that promotes neurogenesis in the developing V-SVZ. Graphical Abstract. Jedi-1-dependent phagocytosis supports neurogenesis via suppression of microglial inflammatory pathway activationTop: Wild-type Proliferative-zone-Associated Microglia (PAMs) (cyan) use the engulfment receptor Jedi-1 ( Jedi) to engulf apoptotic cells (yellow) in the neurogenic ventricular-subventricular zone (V-SVZ) of the early postnatal brain. Jedi activation supports neural precursor cell (NPC) proliferation and the generation of new neurons. Bottom: Deletion of Jedi reduces microglial phagocytosis and transforms PAMs into Disease-associated Inflammatory Microglia (DIMs) characterized by the upregulation of canonical inflammatory genes and core DIM markers iden ified in the aging and neurodegenerative brain (Nlrp3, NLR family pyrin domain-containing 3; Tnf, tumor necrosis factor; Ccl4, C-C chemokine ligand 4 (also called macrophage inflammatory protein 1{beta}); Ccr5, C-C chemokine receptor type 5). Increased interleukin-1{beta} (IL-1{beta}) synthesis, release, and signaling in the Jedi-null V-SVZ reduces NPC proliferation and newborn neuron number. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=119 SRC="FIGDIR/small/531012v1_ufig1.gif" ALT="Figure 1"> View larger version (34K): org.highwire.dtl.DTLVardef@16b9785org.highwire.dtl.DTLVardef@a8be50org.highwire.dtl.DTLVardef@66b726org.highwire.dtl.DTLVardef@1825d8b_HPS_FORMAT_FIGEXP M_FIG C_FIG HighlightsO_LIThe engulfment receptor Jedi-1 is expressed by microglia in the neonatal ventricular-subventricular zone (V-SVZ) neurogenic niche. C_LIO_LIJedi-1 knockout microglia have decreased engulfment ability, resulting in accumulation of dead cells in the V-SVZ. C_LIO_LILoss of Jedi-1 leads to a neuroinflammatory phenotype in microglia that is characteristic of neurodegenerative and age-associated microglia. C_LIO_LIMicroglial-specific loss of Jedi-1 reduces neurogenesis, which is rescued in vivo by inhibition of interleukin-1{beta} signaling. C_LI

neuroscience↗