Biology subjects

Balogh, E.

Publications and source records attributed to Balogh, E..

5 recordsLinked to original sources

bioRxiv2024

Do pyrethroid insecticides influence sex ratios in agile frogs (Rana dalmatina)?

Environmental pollutants have the potential to alter sex ratios in wildlife through sex-biased mortality. Furthermore, endocrine disruptors may cause sex reversal during early ontogeny in ectothermic vertebrates, resulting in a phenotypic sex that is not concordant with the genotypic sex encoded by the sex chromosomes. Despite the wide-ranging implications of these sex-ratio biasing effects, they are rarely studied in ecotoxicology, especially in a way that allows for disentangling the two mechanisms. We investigated these effects of two synthetic pyrethroids, deltamethrin and etofenprox, that are commonly used insecticides and have been linked to adverse effects on fish and amphibian biodiversity. We assessed the effects of environmentally relevant concentrations of these two pyrethroids on phenotypic sex ratio, sex-dependent mortality, and sex reversal in agile frogs (Rana dalmatina). Tadpoles from field-collected eggs were reared in mesocosm until metamorphosis by adding 0.03 or 0.3 g/L of deltamethrin or etofenprox three times to the water. We observed no effect in three of the four treatment groups. However, in the lower-concentration etofenprox treatment, phenotypic sex ratio was male-biased two months post-metamorphosis, and genotypic sexing revealed that this was due to female-biased mortality during metamorphosis and not to sex reversal. Although the estimation certainty of these effects was somewhat limited, they highlight that not all sex-ratio distorting effects are caused by sex reversal. Therefore, ecotoxicological studies aiming to understand the endocrine distruptor effects of environmental contaminants should strive to separate the effects on sex determination and sex-dependent mortality.

ecology↗

bioRxiv2023

Infection with the chytrid fungus (Batrachochytrium dendrobatidis) may distort sex ratio via sex reversal but not sex-dependent mortality in a common Eurasian amphibian

One of the major factors driving the currently ongoing biodiversity crisis is the anthropogenic spread of infectious diseases. Diseases can have conspicuous consequences, such as mass mortality events, but may also exert covert but similarly severe effects, such as sex ratio distortion via sex-biased mortality or sex reversal. Chytridiomycosis, caused by the fungal pathogen Batrachochytrium dendrobatidis (Bd) is among the most important threats to amphibian biodiversity. Yet, whether Bd infection can skew sex ratios in amphibians is currently unknown, although such a hidden effect may cause the already dwindling amphibian populations to collapse. To investigate this possibility, we collected common toad (Bufo bufo) tadpoles from a natural habitat in Hungary, and continuously treated them until metamorphosis with sterile Bd culture medium (control), or a liquid culture of a Hungarian or a Spanish Bd isolate. Three months after metamorphosis we dissected the individuals and diagnosed their phenotypic and genetic sex. Bd prevalence was high in animals that died during the experiment but was almost zero at sexing. Survival was generally low in the control group, but it was further lowered by the Bd treatments. We did not observe sex-dependent mortality in either treatment. However, treatment with the Spanish Bd isolate significantly increased the frequency of sex reversal: 3 out of 9 genetic females developed into phenotypic males. Based on our results, Bd infection may have the potential to affect sex ratio in common toads through female-to-male sex reversal, but future research is needed to ascertain the generality of these findings.

developmental biology↗

bioRxiv2023

Tadpoles develop elevated heat tolerance in urban heat islands regardless of sex

The ability of wildlife to endure the effects of high temperatures is increasingly important for biodiversity conservation under climate change and spreading urbanization. Organisms living in urban heat islands can have elevated heat tolerance via both phenotypic plasticity and microevolution. However, the prevalence and mechanisms of such thermal adaptations are barely known in aquatic organisms. Furthermore, males and females can differ in heat tolerance, which may lead to sex-biased mortality, yet it is unknown how sex differences in thermal biology influence urban adaptations. To address these knowledge gaps, we measured critical thermal maxima (CTmax) in male and female agile frog (Rana dalmatina) tadpoles captured from warm urban ponds and cool woodland ponds, and in a common-garden experiment where embryos collected from both habitat types were raised in the laboratory. We found higher CTmax in urban-dwelling tadpoles compared to their counterparts living in woodland ponds. This difference was reversed in the common-garden experiment: tadpoles originating from urban ponds had lower CTmax than tadpoles originating from woodland ponds. We found no effect of sex on CTmax or its difference between habitats. These results demonstrate that aquatic amphibian larvae can respond to the urban heat island effect with increased heat tolerance similarly to the other, mostly terrestrial taxa studied so far, and that phenotypic plasticity may be the main driver of this response. Our findings also suggest that heat-induced mortality may be independent of sex in tadpoles, but research is needed in many more taxa to explore potentially sex-dependent urban thermal responses.

evolutionary biology↗

bioRxiv2023

Hypoxia-inducible factor (HIF) activation promotes osteogenic transition of valve interstitial cells and accelerates heart valve calcification in chronic kidney disease (CKD)

AimsValve calcification (VC) is a widespread complication in chronic kidney disease (CKD) patients on hemodialysis. VC is an active process with the involvement of in situ osteogenic transition of valve interstitial cells (VICs). VC is accompanied by the activation of hypoxia inducible factor (HIF) pathway, but the role of HIF activation in the calcification process remains undiscovered. Methods and resultUsing in vitro and in vivo approaches we addressed the role of HIF activation in osteogenic transition of VICs and CKD-associated VC. Elevation of osteogenic (Runx2, Sox9) and HIF activation markers (HIF-1 and HIF-2) and VC occurred in adenine-induced CKD mice. High phosphate (Pi) induced upregulation of osteogenic (Runx2, alkaline-phosphatase, Sox9, osteocalcin) and hypoxia markers (HIF-1, HIF-2, Glut-1), and calcification in VICs. Down-regulation of HIF-1 and HIF-2 inhibited, whereas further activation of HIF pathway by hypoxic exposure (1% O2) or hypoxia mimetics (desferrioxamine, CoCl2, Daprodustat (DPD)) promoted Pi-induced calcification of VICs. Pi augmented the formation of reactive oxygen species (ROS) and decreased viability of VICs, whose effects were further exacerbated by hypoxia. N-acetyl cysteine inhibited Pi-induced ROS production, cell death and calcification under both normoxic and hypoxic conditions. DPD treatment corrected anemia but promoted VC in the CKD mice model. ConclusionsHIF activation plays a fundamental role in Pi-induced osteogenic transition of VICs and CKD-induced VC. The cellular mechanism involves stabilization of HIF-1 and HIF-2, increased ROS production and cell death. Targeting the HIF pathways may thus be investigated as a therapeutic approach to attenuate VC. Translational perspectiveOne in four hemodialysis-dependent CKD patients on DPD treatment experience a major cardiovascular event during a 2.5-year follow-up period. This work provides a possible explanation for this phenomenon and should initiate further studies to address whether DPD-mediated acceleration of valve calcification triggers the unbeneficial effect of DPD.

pathology↗

bioRxiv2021

Novel genetic sex markers reveal unexpected lack of, and similar susceptibility to, sex reversal in free-living common toads in both natural and anthropogenic habitats

Anthropogenic environmental changes are affecting biodiversity and microevolution worldwide. Ectothermic vertebrates are especially vulnerable, since their sexual development can be disrupted by environmental changes, which can cause sex reversal, a mismatch between genetic and phenotypic sex, potentially leading to sex-ratio distortion and population decline. Despite these implications, we have scarce empirical knowledge on the incidence of sex reversal in nature. Populations in anthropogenic environments may experience sex reversal more frequently, or alternatively, they may adapt to resist sex reversal. To test these alternative hypotheses, we developed PCR-based genetic sex markers for the common toad (Bufo bufo). We assessed the prevalence of sex reversal in wild populations living in natural, agricultural and urban habitats, and the susceptibility of the same populations to two ubiquitous estrogenic pollutants in a common-garden experiment. We found negligible sex-reversal frequency in free-living adults despite the presence of various endocrine-disrupting pollutants in their breeding ponds. Individuals from different habitat types showed similar susceptibility to sex reversal in the laboratory: all genetic males developed female phenotype when exposed to 1 {micro}g/L 17- ethinylestradiol (EE2) during larval development, whereas no sex reversal occurred in response to 1 ng/L EE2 and a glyphosate-based herbicide with 3 {micro}g/L or 3 mg/L glyphosate. The latter results do not support that populations in anthropogenic habitats would have either increased propensity for or higher tolerance to chemically induced sex reversal. Thus, the surprisingly low sex-reversal frequency in wild toads compared to other ectothermic vertebrates studied before might indicate idiosyncratic, potentially species-specific resistance to sex reversal.

ecology↗