Assessing the antibacterial properties of eggshell-titanium powder

The global distribution of oral diseases caused by bacterial and the severity of their consequences constitute a pandemic condition.The present paper reports on the antibacterial properties of a modified eggshell and titanium dioxide using the mechanochemical method. EB@TiO2 was modified and characterized using X-raydiffraction (XRD) while the degradation condition was studied using Thermogravimetric analysis (TGA).The inhibitory properties of EB@TiO2at differentconcentrations (2:1; 3:1 and 4: 1) against both Grampositive (E. coli) and negative bacterial (B. Cereus)strain were studied the using disk diffusion method.The XRD result confirmed the presence of a thermodynamically stable calcite structure, which is indicative of calcium carbonate. The diffraction peak of the XRD at 2θ = 29.5o suggests the deposition of TiO2 on the surface of CaCo3. TGA curves shows the decomposition of anatase form of titanium dioxide and calcium carbonate. The study evidently shows the antibacterial activities of EB@TiO2 against Escherichia coli and B. Cereus. The salient feature of the study finding is that modifying eggshells with titanium dioxide improves the antibacterial properties, and thus offers a promising role for the development of potent

Intercolony variation in reproductive skipping in the African penguin

This is the final version. Available on open access from Wiley via the DOI in this recordData availability statement: The data underlying this article are available in the Dryad digital repository: https://doi.org/10.5061/dryad.0rxwdbs3z (Leith et al., 2022).In long-lived species, reproductive skipping is a common strategy whereby sexually mature animals skip a breeding season, potentially reducing population growth. This may be an adaptive decision to protect survival, or a non-adaptive decision driven by individual-specific constraints. Understanding the presence and drivers of reproductive skipping behavior can be important for effective population management, yet in many species such as the endangered African penguin (Spheniscus demersus), these factors remain unknown. This study uses multistate mark-recapture methods to estimate African penguin survival and breeding probabilities at two colonies between 2013 and 2020. Overall, survival (mean ± SE) was higher at Stony Point (0.82 ± 0.01) than at Robben Island (0.77 ± 0.02). Inter-colony differences were linked to food availability; under decreasing sardine (Sardinops sagax) abundance, survival decreased at Robben Island and increased at Stony Point. Additionally, reproductive skipping was evident across both colonies; at Robben Island the probability of a breeder becoming a nonbreeder was ~0.22, versus ~0.1 at Stony Point. Penguins skipping reproduction had a lower probability of future breeding than breeding individuals; this lack of adaptive benefit suggests reproductive skipping is driven by individual-specific constraints. Lower survival and breeding propensity at Robben Island places this colony in greater need of conservation action. However, further research on the drivers of inter-colony differences is needed.Association of Zoos and AquariumsBristol Zoological SocietyDepartment of Forestry, Fisheries, and the EnvironmentEarthwatch InstitutePew Charitable TrustsLeiden Conservation FoundationSANCCOBSan Diego Zoo Wildlife Allianc

Unravelling mechanism for detecting chromium on functionalized gold nanoparticles via a smartphone and spectrophotometric-based systems supported by CIEL*a*b* colour space and molecular dynamics

DATA AVAILABILITY : No data was used for the research described in the article.This paper demonstrates the application of smartphones as well as spectrophotometers as tools to demystify the mechanism leading to colour variation of 1,5-diphenylcarbazide functionalized gold nanoparticles (DPC-AuNPs) due to chromium addition. Colour Grab 3.6.1 app was used to capture and decode colours from samples containing DPC-AuNPs with different concentrations of hexavalent Chromium [Cr(VI)] standards. The presence of Cr(VI) aggregated DPC-AuNPs resulted in a colour change from pink to blue and a decrease in the peak intensity as accompanied by a red shift of the SPR peak to 670 nm. The R colour coordinates decreased as Cr(VI) concentration was increased to 16 µM then a rapid decrease was noted between 18–25 µM and G and B colour coordinates followed the same trend. Colour difference (∆E) increased significantly as the Cr(VI) concentration increased. A rapid decrease was noticed in the hue angle between 16–25 µM while chroma decreased significantly as the Cr(VI) concentration increased. Molecular dynamics calculation of a gold cluster was used to simulate the aggregation process. The calculated radial distribution [g(r)] from cluster models of the Cr-DPC complex was two-fold more than Cr-AuNPs. This was associated with the aggregation of gold nanoparticles leading to the appearance of the blue colour of AuNPs solution which was also supported by the intensity obtained from colour Grab. This study will potentially be applied in the future for the fabrication of a Lovibond photometer for the detection of metal ions in environmental samples.Mintek, the National Research Foundation (South Africa), ESKOM Tertiary Education Support Programme (South Africa) and Moses Kotane Institute as well as the Centre for Higher Computer Performance in Cape Town.http://www.elsevier.com/ locate/molstruchj2024PhysicsNon

Southern Africa's great escarpment as an amphitheater of climate-driven diversification and a buffer against future climate change in bats

DATA AVAILABILITY STATEMENT : Raw cyt-b sequence data (FASTA files; Datasets S1–S3) and craniometric and specimen data (Excel files; Datasets S4–S7) are openly available on Dryad at https://doi.org/10.5061/dryad.3bk3j9ksc.Hosting 1460 plant and 126 vertebrate endemic species, the Great Escarpment (hereafter, Escarpment) forms a semi-circular “amphitheater” of mountains girdling southern Africa from arid west to temperate east. Since arid and temperate biota are usually studied separately, earlier studies overlooked the biogeographical importance of the Escarpment as a whole. Bats disperse more widely than other mammalian taxa, with related species and intraspecific lineages occupying both arid and temperate highlands of the Escarpment, providing an excellent model to address this knowledge gap. We investigated patterns of speciation and micro-endemism from modeled past, present, and future distributions in six clades of southern African bats from three families (Rhinolophidae, Cistugidae, and Vespertilionidae) having different crown ages (Pleistocene to Miocene) and biome affiliations (temperate to arid). We estimated mtDNA relaxed clock dates of key divergence events across the six clades in relation both to biogeographical features and patterns of phenotypic variation in crania, bacula and echolocation calls. In horseshoe bats (Rhinolophidae), both the western and eastern “arms” of the Escarpment have facilitated dispersals from the Afrotropics into southern Africa. Pleistocene and pre-Pleistocene “species pumps” and temperate refugia explained observed patterns of speciation, intraspecific divergence and, in two cases, mtDNA introgression. The Maloti-Drakensberg is a center of micro-endemism for bats, housing three newly described or undescribed species. Vicariance across biogeographic barriers gave rise to 29 micro-endemic species and intraspecific lineages whose distributions were congruent with those identified in other phytogeographic and zoogeographic studies. Although Köppen–Geiger climate models predict a widespread replacement of current temperate ecosystems in southern Africa by tropical or arid ecosystems by 2070–2100, future climate Maxent models for 13 bat species (all but one of those analyzed above) showed minimal range changes in temperate species from the eastern Escarpment by 2070, possibly due to the buffering effect of mountains to climate change.National Research Foundation and Department of Science and Innovation of South Africa; Afromontane Research Unit, University of the Free State; National Research Foundation.http://www.wileyonlinelibrary.com/journal/gcbhj2024Medical VirologySDG-15:Life on lan

A distribution model for Glossina brevipalpis and Glossina austeni in southern Mozambique, Eswatini and South Africa for enhanced area-wide integrated pest management approaches

BACKGROUND : Glossina austeni and Glossina brevipalpis (Diptera: Glossinidae) are the sole cyclical vectors of African trypanosomes in South Africa, Eswatini and southern Mozambique. These populations represent the southernmost distribution of tsetse flies on the African continent. Accurate knowledge of infested areas is a prerequisite to develop and implement efficient and cost-effective control strategies, and distribution models may reduce large-scale, extensive entomological surveys that are time consuming and expensive. The objective was to develop a MaxEnt species distribution model and habitat suitability maps for the southern tsetse belt of South Africa, Eswatini and southern Mozambique. METHODOLOGY/PRINCIPAL FINDINGS : The present study used existing entomological survey data of G. austeni and G. brevipalpis to develop a MaxEnt species distribution model and habitat suitability maps. Distribution models and a checkerboard analysis indicated an overlapping presence of the two species and the most suitable habitat for both species were protected areas and the coastal strip in KwaZulu-Natal Province, South Africa and Maputo Province, Mozambique. The predicted presence extents, to a small degree, into communal farming areas adjacent to the protected areas and coastline, especially in the Matutuíne District of Mozambique. The quality of the MaxEnt model was assessed using an independent data set and indicated good performance with high predictive power (AUC > 0.80 for both species). CONCLUSIONS/SIGNIFICANCE : The models indicated that cattle density, land surface temperature and protected areas, in relation with vegetation are the main factors contributing to the distribution of the two tsetse species in the area. Changes in the climate, agricultural practices and land-use have had a significant and rapid impact on tsetse abundance in the area. The model predicted low habitat suitability in the Gaza and Inhambane Provinces of Mozambique, i.e., the area north of the Matutuíne District. This might indicate that the southern tsetse population is isolated from the main tsetse belt in the north of Mozambique. The updated distribution models will be useful for planning tsetse and trypanosomosis interventions in the area.S1 Fig. Uncertainty grid for the habitat suitability index model for Glossina austeni and Glossina brevipalpis (https://dataverse.harvard.edu/dataset.xhtml?persistentId=doi:10. 7910/DVN/PA7U7L).The Joint Food and Agriculture Organization of the United Nations (FAO)/ International Atomic Energy Agency (IAEA) Centre of Nuclear Techniques in Food and Agriculture and the IAEA’s Department of Technical Cooperation; the IAEA’s Department of Technical Cooperation; the Department of Science and Technology and the GeosAf project.http://www.plosntds.orgam2022Veterinary Tropical Disease

Mycobacterial dihydrofolate reductase inhibitors identified using chemogenomic methods and in vitro validation.

The lack of success in target-based screening approaches to the discovery of antibacterial agents has led to reemergence of phenotypic screening as a successful approach of identifying bioactive, antibacterial compounds. A challenge though with this route is then to identify the molecular target(s) and mechanism of action of the hits. This target identification, or deorphanization step, is often essential in further optimization and validation studies. Direct experimental identification of the molecular target of a screening hit is often complex, precisely because the properties and specificity of the hit are not yet optimized against that target, and so many false positives are often obtained. An alternative is to use computational, predictive, approaches to hypothesize a mechanism of action, which can then be validated in a more directed and efficient manner. Specifically here we present experimental validation of an in silico prediction from a large-scale screen performed against Mycobacterium tuberculosis (Mtb), the causative agent of tuberculosis. The two potent anti-tubercular compounds studied in this case, belonging to the tetrahydro-1,3,5-triazin-2-amine (THT) family, were predicted and confirmed to be an inhibitor of dihydrofolate reductase (DHFR), a known essential Mtb gene, and already clinically validated as a drug target. Given the large number of similar screening data sets shared amongst the community, this in vitro validation of these target predictions gives weight to computational approaches to establish the mechanism of action (MoA) of novel screening hit

Structural Insights into the Quinolone Resistance Mechanism of Mycobacterium tuberculosis DNA Gyrase

Mycobacterium tuberculosis DNA gyrase, an indispensable nanomachine involved in the regulation of DNA topology, is the only type II topoisomerase present in this organism and is hence the sole target for quinolone action, a crucial drug active against multidrug-resistant tuberculosis. To understand at an atomic level the quinolone resistance mechanism, which emerges in extensively drug resistant tuberculosis, we performed combined functional, biophysical and structural studies of the two individual domains constituting the catalytic DNA gyrase reaction core, namely the Toprim and the breakage-reunion domains. This allowed us to produce a model of the catalytic reaction core in complex with DNA and a quinolone molecule, identifying original mechanistic properties of quinolone binding and clarifying the relationships between amino acid mutations and resistance phenotype of M. tuberculosis DNA gyrase. These results are compatible with our previous studies on quinolone resistance. Interestingly, the structure of the entire breakage-reunion domain revealed a new interaction, in which the Quinolone-Binding Pocket (QBP) is blocked by the N-terminal helix of a symmetry-related molecule. This interaction provides useful starting points for designing peptide based inhibitors that target DNA gyrase to prevent its binding to DNA