Periplasmic bacterial biomineralization of copper sulfide nanoparticles

Metal sulfides are a common group of extracellular bacterial biominerals. Only few cases of intracellular biomineralization have been reported in this group, mostly limited to greigite (Fe3S4) in magnetotactic bacteria. Here, we report the intracellular but periplasmic biomineralization of copper sulfide by the magnetotactic bacterium Desulfamplus magnetovallimortis (strain BW-1) that is known to mineralize greigite and magnetite (Fe3O4) in the cytoplasm. BW-1 produces hundreds of spherical nanoparticles, composed of 1-2 nm substructures of a poorly crystalline hexagonal copper sulfide that remains in a thermodynamically unstable state. Differential proteomics suggests that periplasmic proteins, such as a DegP-like protein and a heavy metal-binding protein, could be involved in this process. The unexpected periplasmic formation of copper sulfide nanoparticles in BW-1 reveals previously unknown possibilities for intracellular biomineralization.

Risk factors and prediction model of severe pertussis in infants < 12 months of age in Tianjin, China

Background To identify risk factors associated with the prognosis of pertussis in infants (< 12 months). Methods A retrospective study on infants hospitalized with pertussis January 2017 to June 2019. The infants were divided into two groups according to the severity of disease: severe pertussis and non-severe pertussis groups. We collected all case data from medical records including socio-demographics, clinical manifestations, and auxiliary examinations. Univariate analysis and Logistic regression were used. Results Finally, a total of 84 infants with severe pertussis and 586 infants with non-severe pertussis were admitted. The data of 75% of the cases (severe pertussis group, n = 63; non-severe pertussis group, n = 189) were randomly selected for univariate and multivariate logistic regression analysis. The results showed rural area [P = 0.002, OR = 6.831, 95% CI (2.013–23.175)], hospital stay (days) [P = 0.002, OR = 1.304, 95% CI (1.107–1.536)], fever [P = 0.040, OR = 2.965, 95% CI (1.050–8.375)], cyanosis [P = 0.008, OR = 3.799, 95% CI (1.419–10.174)], pulmonary rales [P = 0.021, OR = 4.022, 95% CI (1.228–13.168)], breathing heavily [P = 0.001, OR = 58.811, 95% CI (5.503–628.507)] and abnormal liver function [P < 0.001, OR = 9.164, 95% CI (2.840–29.565)] were independent risk factors, and higher birth weight [P = 0.006, OR = 0.380, 95% CI (0.191–0.755)] was protective factor for severe pertussis in infants. The sensitivity and specificity of logistic regression model for remaining 25% data of severe group and common group were 76.2% and 81.0%, respectively, and the consistency rate was 79.8%. Conclusions The findings indicated risk factor prediction models may be useful for the early identification of severe pertussis in infants.

Calcatedessa gen.n. a new genus sister to Grammedessa Correia & Fernandes (Heteroptera, Pentatomidae, Edessinae) based on a cladistic analysis

Grammedessa Correia & Fernandes, 2016 is a genus raised to include some species of Edessa Fabricius, 1803 that is a very common group of stink bugs inhabiting only the Neotropical region. Grammedessa was proposed excluding a few species that were morphologically similar but not completely fitting in the diagnostic requirements of the genus. Grammedessa was also proposed without considering a phylogenetic context. In this work, the monophyly of Grammedessa was tested using a cladistic analysis, including all species that were originally excluded, under both Maximum Parsimony and Bayesian methods. As a result, six new species are now included in Grammedessa, which will be described in a forthcoming paper; Edessa botocudo Kirkaldy, 1909 was considered an unnecessary new name for Edessa hamata Walker, 1868 that was transferred to Grammedessa, resulting in G. hamata (Walker, 1868) comb.n. Calcatedessa gen.n., a new genus sister to Grammedessa, is here proposed to include four new species: C. anthomorpha sp.n., C. clarimarginata sp.n., C. germana sp.n. and C. temnomarginata sp.n. The Calcatedessa–Grammedessa clade and both genera were recovered as monophyletic by Maximum Parsimony and Bayesian methods. An identification key to the species of Calcatedessa gen.n. is provided. The new genus is distributed in Guyana, Suriname, French Guyana, and Brazil.

Riboceine Rescues Auranofin-Induced Craniofacial Defects in Zebrafish

Craniofacial abnormalities are a common group of congenital developmental disorders that can require intensive oral surgery as part of their treatment. Neural crest cells (NCCs) contribute to the facial structures; however, they are extremely sensitive to high levels of oxidative stress, which result in craniofacial abnormalities under perturbed developmental environments. The oxidative stress-inducing compound auranofin (AFN) disrupts craniofacial development in wildtype zebrafish embryos. Here, we tested whether the antioxidant Riboceine (RBC) rescues craniofacial defects arising from exposure to AFN. RBC rescued AFN-induced cellular apoptosis and distinct defects of the cranial cartilage in zebrafish larvae. Zebrafish embryos exposed to AFN have higher expression of antioxidant genes gstp1 and prxd1, with RBC treatment partially rescuing these gene expression profiles. Our data suggest that antioxidants may have utility in preventing defects in the craniofacial cartilage owing to environmental or genetic risk, perhaps by enhancing cell survival.

Comparative Analysis of Equivalence of Somatic Phraseological Units in German and Uzbek Languages

This article is devoted to a comparative analysis of somatic phraseological units in German and Uzbek. Somatic phraseological units are part of a common group of phrases in German and Uzbek. Many languages have equivalents of somatic phraseological units, however, each part of the body is associated with certain characteristics: head with mind, heart with feelings, mouth and tongue with speech, hands with practical activity. The work contains about 1500 somatic phrases based on explanatory phraseological dictionaries and multilingual phraseographic sources of German and Uzbek languages, which are studied in terms of lexic, syntax and semantics. The work explores somatic expressions in both languages from a lexical, syntactic and semantic point of view. In the somatic phraseological units, the human body participates as a nuclear word, and they have cultural signs of a certain mentality. From the point of view of structural-semantic and structural-syntactic interactions, somatisms in German and Uzbek were studied in such categories as absolute equivalence, partial equivalence, zero equivalence. In this work, phraseological units corresponding to all lexical, morphological and syntactic criteria of equivalence are interpreted as absolute, having almost the same meaning in both languages, as well as small morphological-syntactic and lexical-semantic differences - as partially equivalent, without alternative equivalents or lexical options in comparable languages according to internal and external linguistic factors, as zero equivalents. The results of the study are presented in tables as statistical data.

MOLECULAR GENETIC ANALYSIS OF RABIES VIRUS IN THE EAST KAZAKHSTAN REGION

Phylogenetic study of genomes of field isolates of lissavirus extracted from the territory of East Kazakhstan is presented in the article in order to carry out sequencing analysis. Ten samples purified PCR products containing rabies virus were examined. As a result of sequencing analysis, ten complete sequences of rabies virus nucleoprotein from East Kazakhstan region were grouped into 6 genotypes, which belong to two lyssavirus groups: Arctic-like group and the most common group - the Steppe group.

Religious identity cues increase vaccination intentions and trust in medical experts among American Christians

Containing the COVID-19 pandemic in the United States requires mobilizing a large majority of the mass public to vaccinate, but many Americans are hesitant or opposed to vaccination. A significant predictor of vaccine attitudes in the United States is religiosity, with more-religious individuals expressing more distrust in science and being less likely to get vaccinated. Here, we test whether explicit cues of common religious identity can help medical experts build trust and increase vaccination intentions. In a preregistered survey experiment conducted with a sample of unvaccinated American Christians (n = 1,765), we presented participants with a vaccine endorsement from a prominent medical expert (NIH Director Francis Collins) and a short essay about doctors’ and scientists’ endorsement of the vaccines. In the common religious identity condition, these materials also highlighted the religious identity of Collins and many medical experts. Unvaccinated Christians in the common identity condition expressed higher trust in medical experts, greater intentions to vaccinate, and greater intentions to promote vaccination to friends and family than those who did not see the common identity cue. These effects were moderated by religiosity, with the strongest effects observed among the most religious participants, and statistically mediated by heightened perceptions of shared values with the medical expert endorsing the vaccine. These findings demonstrate the efficacy of common identity cues for promoting vaccination in a vaccine-hesitant subpopulation. More generally, the results illustrate how trust in science can be built through the invocation of common group identities, even identities often assumed to be in tension with science.

Cone photoreceptor dysfunction in retinitis pigmentosa revealed by optoretinography

Retinitis pigmentosa (RP) is the most common group of inherited retinal degenerative diseases, whose most debilitating phase is cone photoreceptor death. Perimetric and electroretinographic methods are the gold standards for diagnosing and monitoring RP and assessing cone function. However, these methods lack the spatial resolution and sensitivity to assess disease progression at the level of individual photoreceptor cells, where the disease originates and whose degradation causes vision loss. High-resolution retinal imaging methods permit visualization of human cone cells in vivo but have only recently achieved sufficient sensitivity to observe their function as manifested in the cone optoretinogram. By imaging with phase-sensitive adaptive optics optical coherence tomography, we identify a biomarker in the cone optoretinogram that characterizes individual cone dysfunction by stimulating cone cells with flashes of light and measuring nanometer-scale changes in their outer segments. We find that cone optoretinographic responses decrease with increasing RP severity and that even in areas where cone density appears normal, cones can respond differently than those in controls. Unexpectedly, in the most severely diseased patches examined, we find isolated cones that respond normally. Short-wavelength–sensitive cones are found to be more vulnerable to RP than medium- and long-wavelength–sensitive cones. We find that decreases in cone response and cone outer-segment length arise earlier in RP than changes in cone density but that decreases in response and length are not necessarily correlated within single cones.

EZHIP: a new piece of the puzzle towards understanding pediatric posterior fossa ependymoma

Ependymomas (EPN) are tumors of the central nervous system (CNS) that can arise in the supratentorial brain (ST-EPN), hindbrain or posterior fossa (PF-EPN) or anywhere in the spinal cord (SP-EPN), both in children and adults. Molecular profiling studies have identified distinct groups and subtypes in each of these anatomical compartments. In this review, we give an overview on recent findings and new insights what is driving PFA ependymomas, which is the most common group. PFA ependymomas are characterized by a young median age at diagnosis, an overall balanced genome and a bad clinical outcome (56% 10-year overall survival). Sequencing studies revealed no fusion genes or other highly recurrently mutated genes, suggesting that the disease is epigenetically driven. Indeed, recent findings have shown that the characteristic global loss of the repressive histone 3 lysine 27 trimethylation (H3K27me3) mark in PFA ependymoma is caused by aberrant expression of the enhancer of zeste homolog inhibitory protein (EZHIP) or in rare cases by H3K27M mutations, which both inhibit EZH2 thereby preventing the polycomb repressive complex 2 (PRC2) from spreading H3K27me3. We present the current status of the ongoing work on EZHIP and its essential role in the epigenetic disturbance of PFA biology. Comparisons to the oncohistone H3K27M and its role in diffuse midline glioma (DMG) are drawn, highlighting similarities but also differences between the tumor entities and underlying mechanisms. A strong focus is to point out missing information and to present directions of further research that may result in new and improved therapies for PFA ependymoma patients.