Biology subjects

Enriquez, S.

Publications and source records attributed to Enriquez, S..

5 recordsLinked to original sources

bioRxiv2026

The SoxC transcription factors regulate multiple early retinal lineages and function in parallel with Atoh7 to promote retinal ganglion cell genesis

Retinal development is orchestrated by a network of transcription factors that guide multipotent retinal progenitor cells (RPCs) to fate-committed lineages, ultimately producing seven major retinal cell classes. Among these, retinal ganglion cells (RGCs) serve as the sole output neurons of the retina, relaying visual and non-visual information to the brain. RGC specification requires a cascade of transcriptional regulators, including the basic helix-loop-helix (bHLH) factor Atoh7, which confers competence to RPCs, and Pou4f2 and Isl1, which drive terminal differentiation and subtype diversification. Previous studies demonstrate that the SoxC group transcription factors (Sox4, Sox11, and Sox12) are also involved in RGC genesis, but their precise integration into the Atoh7-driven regulatory hierarchy remains undefined. To address this question, we used the retina-specific Vsx2-Cre line to generate Sox4/Sox11 double conditional knockout (dcKO) and Sox4/Sox11/Atoh7 triple knockout (tKO) mice. Immunohistochemistry revealed profound lineage disruption and reduced progenitor proliferation and survival in both dcKO and tKO retinas; not only RGC genesis but also that of horizontal and amacrine (H&As) cells were severely compromised, whereas photoreceptor cells (PHCs) production increased. These results indicate that Sox4 and Sox11 are involved in the coordinated generation of the different early retinal lineages. Like the Atoh7-null retina, RGC precursors still formed in the SoxC dcKO retina, but their genesis was almost completely abolished in the tKO retina. Our findings indicate that the SoxC factors act in parallel with Atoh7 as a major upstream regulatory input to initiate RGC fate. Bulk RNA-seq revealed the SoxC-dependent transcriptional programs and signaling pathways and confirmed the lineage changes demonstrated by marker analysis. CUT&Tag analysis identified the genome-wide binding sites and thereby the target genes of Sox11, further illuminating the mechanisms underlying functions of the SoxC factors in multiple retinal cell states/types during development.

developmental biology↗

bioRxiv2026

Uncovering parasite diversity in Ecuadorian wildlife: new trypanosomatid species and novel reservoir hosts for Leishmania amazonensis

Wildlife hosts play important roles in the ecology and transmission of vector-borne parasites, yet information on host associations remains scarce in many biodiverse tropical regions. Within a One Health framework, characterizing parasite diversity in wildlife can improve understanding of ecosystem health and disease emergence. Road-killed animals provide a non-invasive opportunity to investigate host-parasite interactions while minimizing disturbance to natural habitats. We screened 127 liver and intestinal tissue samples obtained from 76 road-killed vertebrates collected near protected areas in two Ecuadorian biodiversity hotspots, the Tropical Andes and Choco-Darien, for trypanosomatids and other vector-borne microorganisms. Molecular analyses targeted the 18S rRNA and cytochrome b genes of trypanosomatids and included additional screening for Trypanosoma cruzi, Trypanosoma rangeli, Rickettsia spp., and piroplasmids. Twenty-nine samples were positive for kinetoplastids. We detected diverse trypanosomatids representing the genera Leishmania, Porcisia, Trypanosoma, Phytomonas, Blastocrithidia, and Obscuromonas, as well as free-living kinetoplastids of the order Neobodonida. The most frequently detected species was Leishmania amazonensis, identified in 17 samples from at least 13 species of birds, reptiles, and caecilians, predominantly in liver tissue, suggesting previously unrecognized host associations. We also identified a putatively novel species of Porcisia and three potentially undescribed avian trypanosomes belonging to the subgenus Ornithotrypanum. No evidence of T. cruzi, T. rangeli, Rickettsia spp., or piroplasmids was found. Our findings identify birds, reptiles, and caecilians as potential reservoir hosts of L. amazonensis. In addition, we substantially expanded current knowledge of kinetoplastid diversity in Ecuadorian wildlife. This study demonstrates the value of road-killed animals as a practical, non-invasive resource for wildlife pathogen surveillance and highlights the importance of integrating biodiversity research into One Health approaches to better understand parasite transmission dynamics in rapidly changing tropical ecosystems. Author summaryMany parasites that affect humans circulate naturally in wildlife, but identifying their animal hosts is often difficult in remote, biodiverse regions. We used road-killed animals as a non-invasive source of biological material to investigate parasites in wildlife from two biodiversity hotspots in Ecuador. By analyzing tissues from birds, reptiles, amphibians, and mammals, we found a remarkable diversity of kinetoplastid flagellates, a group that includes the agents of Chagas disease and leishmaniasis. Although we did not detect human-infective trypanosomes, we repeatedly identified Leishmania amazonensis (a species causing human disease) in birds, reptiles, and caecilians. These vertebrate groups have not previously been recognized as potential hosts of this parasite. We also discovered several undescribed trypanosomatid species, emphasizing how little is known about parasite diversity in tropical wildlife. Our results show that road-killed animals can provide valuable information on host-parasite interactions without disturbing living populations. Such surveillance contributes to One Health efforts by improving our understanding of how environmental change, wildlife, and human health are interconnected.

microbiology↗

bioRxiv2026

Maintenance cost of photosynthesis sets key ecological constraints on zooxanthellate corals

Ecological models using light limitation to explain coral depth distribution have largely disregarded the energetic cost of sustaining photosynthetic activity. Here, we quantified photosystem II (PSII) turnover across a depth-simulated light gradient in a zooxanthellate coral, measuring PSII half-life, D1 protein abundance, and PSII-complex gene expression. Maximum photosynthetic capacity remained stable across irradiance levels while respiration rose and PSII turnover accelerated as a power law, imposing increasing ATP demand at the shallowest depths. Declining D1 protein abundance alongside stable transcript levels demonstrated that this escalating maintenance cost operates through post-transcriptional regulation. Consequently, a decreasing fraction of photosynthetic usable energy is available for translocation to the coral host at high irradiance, as the energy required for PSII repair increases. Integrating these physiological constraints into a bio-optical model revealed that the balance between photosynthetic capacity and its maintenance cost defines an optimal depth, the Photosynthetic Usable Energy Supply (PUES) maximum, where host energetic returns are maximized. This framework provides a mechanistic basis for understanding depth distributions in symbiotic corals and extends as a predictive tool for any photosynthetic organism operating under variable irradiance, including forecasting how environmental degradation contracts viable depth ranges.

ecology↗

bioRxiv2025

Adaptation to heat and ocean fertilization, two keys for understanding the massive Sargassum growth in the Atlantic

O_LIA floating ecosystem constituted by three genetic variants of holopelagic Sargassum has extended since 2011 throughout the tropical North Atlantic without spatial restrictions. C_LIO_LIWe characterized the differential capacity and efficiency of each variant to collect light and fix this energy in photosynthesis under variable light and temperature regimes, focusing on the description of key physiological and optical traits the differential response to light and temperature. C_LIO_LIOur results revealed metabolic adaptations of two genetic variants to the warmer conditions of the tropical Atlantic and contrasting efficiencies in light absorption and use in photosynthesis, indicative of distinct competitive abilities under growth limitations. C_LIO_LIWe concluded that the increased fertility of a warmer ocean is the most plausible explanation for the massive presence of holopelagic Sargassum in the tropical Atlantic, which also may explain the current ecological success of the opportunistic strategy of a previously rare variant. The optical and physiological descriptors documented can assist in developing quantitative models for predicting Sargassum biomass in the Atlantic. C_LI

ecology↗

bioRxiv2023

Effects of surface geometry on light exposure, photoacclimation and photosynthetic energy acquisition in zooxanthellate corals

Symbiotic corals display a great array of morphologies, each of which has unique effects on light interception and the photosynthetic performance of in hospite zooxanthellae. Changes in light availability elicit photoacclimation responses to optimize the energy balances in primary producers, extensively documented for corals exposed to contrasting light regimes along depth gradients. Yet, response variation driven by coral colony geometry and its energetic implications on colonies with contrasting morphologies remain largely unknown. In this study, we assessed the effect of the inclination angle of coral surface on light availability, short- and long-term photoacclimation responses, and potential photosynthetic usable energy. Increasing surface inclination angle resulted in an order of magnitude reduction of light availability, following a linear relationship explained by the cosine law and relative changes in the direct and diffuse components of irradiance. The light gradient induced by surface geometry triggered photoacclimation responses comparable to those observed along depth gradients: changes in the quantum yield of photosystem II, photosynthetic parameters, and optical properties and pigmentation of the coral tissue. Differences in light availability and photoacclimation driven by surface inclination led to contrasting energetic performance. Horizontally and vertically oriented coral surfaces experienced the largest reductions in photosynthetic usable energy as a result of excessive irradiance and light-limiting conditions, respectively. This pattern is predicted to change with depth or local water optical properties. Our study concludes that colony geometry plays an essential role in shaping the energy balance and determining the light niche of zooxanthellate corals.

physiology↗