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Cowell, E.

Publications and source records attributed to Cowell, E..

2 recordsLinked to original sources

Widespread symbiosis of ciliate epibionts colonizing gills of shrimps inhabiting vents and seeps across the Pacific Ocean

Although bacterial symbiosis is well-documented in chemosynthetic-based ecosystems, associations with microeukaryotes remain overlooked. In this study, using scanning electron microscopy and 18S rDNA barcoding, we investigate the presence, diversity, and biogeographic patterns of ciliate epibionts associated with two deep-sea caridean shrimp families: Alvinocarididae, and Thoridae. We identified a widespread lineage of ciliates colonizing the gills of different alvinocaridid species, extending their previously known distribution in freshwater and coastal habitats to deep-sea areas down to 3388 m. These ciliates form a distinct clade related to coastal Chonotrichia, but showing clear genetic divergence from the previously-described species. Geographic divergence of these ciliate populations was observed across the Pacific Ocean, with no evident structure related to their host species. These chonotrichian ciliates exhibited variation occurrence across host species, individuals, and regions, indicating a facultative association with their hosts. In contrast, the thorid shrimps harbored rare and phylogenetically diverse ciliates. More rarely, we found ciliates related to known parasitic lineages hosted by both shrimp families, with signs of immune response - black gills - in some individuals colonized by these ciliates. Our results reveal previously overlooked protist-crustacean associations in chemosynthetic ecosystems and highlight the ecological and biogeographic importance of this group in the deep ocean.

microbiology↗

Monocrotaline treatment of the rat predisposes to altered lipopolysaccharide-induced lung responses.

There is a need to understand pathogen driven lung disease and the rat is a laboratory model, widely used to study acute lung injury (ALI). Here the monocrotaline (MCT) rat has been investigated as a model of an inflammatory lung with developing pulmonary hypertension (PH) on which an ALI is superimposed. 14 days following a single systemic dose of MCT, the lung is functionally normal, but stimulation with lipopolysaccharide (LPS) results in an altered response. The MCT/LPS lung is morphologically similar to LPS alone, with respiratory mechanics showing increased elastance, reduced compliance and increased tissue resistance. Bronchioalveolar lavage (BAL) fluid demonstrated a cellular infiltrate, with large macrophage-like cells, increased secreted angiotensin converting enzyme-2 (ACE2) and total protein. The lung transcriptome is pushed towards a pro-inflammatory M1 phenotype, (interferon (IFN)-{Upsilon}, interleukin 6 (IL6), CD68 and CD80) compared to LPS alone. Additionally, the MCT/LPS lung has gene transcription signatures for enhanced cell death and DNA damage responses, higher levels of multiple complement components, dysregulation of the renin-angiotensin pathway with reduced ACE2 and increased AGTR1, increased factors such as Erythroferrone that would increase iron levels, and increased fibrinogen and A2M, that would promote thrombosis. Thus, the MCT-treated rat represents an animal with no overt clinical distinction but following LPS stimulation elicits an exacerbated pathogenic lung response. The MCT-treated rat is a simple model that might be beneficial for understanding an M1 lung pathology with activated complement, low ACE2, high iron, and a propensity to clot in the context of developing cardiovascular disease.

physiology↗