Development of alpha-cypermethrin resistance and its effect on biological parameters of yellow fever mosquito, Aedes aegypti (L.) (Diptera: Culicidae).

Alpha-cypermethrin interacts with the sodium channel and causes nerve blockage in insects. It is used to manage Aedes aegypti (Linnaeus) (Diptera: Culicidae), a primary vector of dengue worldwide. It not only affects both target and non-target organisms, but overuse of this insecticide increases the chances of resistance development in insect pests. In this study, resistance development, biological parameters, and stability of alpha-cypermethrin resistance were studied in a laboratory-selected strain of Ae. aegypti. The alpha-cypermethrin selected strain (Alpha Sel) developed an 11.86-fold resistance level after 12 rounds of alpha-cypermethrin selection compared to the unselected strain (Unsel). In biological parameters, Alpha Sel and Cross1 (Unsel ♂ and Alpha Sel♀) had shorter larval durations compared to Unsel and Cross2 (Unsel ♀ and Alpha Sel ♂) populations. The pupal duration of Alpha Sel and both crosses was shorter than that in the Unsel strain. The relative fitness of Alpha Sel, Cross1, and Cross2 was significantly less than that of the Unsel strain. These results indicate that alpha-cypermethrin resistance comes with fitness costs. Moreover, the frequency of alpha-cypermethrin resistance decreased when the Alpha Sel population was reared without further selection pressure for four generations. So, resistance was unstable and reversed when insecticide pressure ceased. We concluded that the judicious and rotational use of different insecticides with different modes of action and the adoption of other IPM-recommended practices would suppress resistance development for more extended periods in Ae. aegypti.

Synthesis and characterization of an α-Fe2O3/ZnTe heterostructure for photocatalytic degradation of Congo red, methyl orange and methylene blue.

The leading challenge towards environmental protection is untreated textile dyes. Tailoring photocatalytic materials is one of the sustainable remediation strategies for dye treatment. Hematite (α-Fe2O3), due to its favorable visible light active band gap (i.e. 2.1 eV), has turned out to be a robust material of interest. However, impoverished photocatalytic efficiency of α-Fe2O3 is ascribable to the short life span of the charge carriers. Consequently, the former synthesized heterostructures possess low degradation efficiency. The aim of the proposed endeavor is the synthesis of a novel zinc telluride-modified hematite (α-Fe2O3/ZnTe) heterostructure, its characterization and demonstration of its enhanced photocatalytic response. The promising heterostructure as well as bare photocatalysts were synthesized via a hydrothermal approach. All photocatalysts were characterized by the X-ray diffraction technique (XRD), scanning electron microscopy (SEM), and electron diffraction spectroscopy (EDX). Moreover, the selectivity and activity of the photocatalyst are closely related to the alignment of its band energy levels, which were estimated by UV-Vis diffuse reflectance spectroscopy (DRS) and X-ray photoelectron spectroscopy (XPS). Nanomaterials, specifically α-Fe2O3 and α-Fe2O3/ZnTe, were used for the degradation of Congo red (97.9%), methyl orange (84%) and methylene blue (73%) under light irradiation (>200 nm) for 60 min. The results suggested that with the aforementioned optimized fabricated heterostructure, the degradation efficiency was improved in comparison to bare hematite (α-Fe2O3). The key rationale towards such improved photocatalytic response is the establishment of a type-II configuration in the α-Fe2O3/ZnTe heterostructure.

Decellularized human cornea for reconstructing the corneal epithelium and anterior stroma.

In this project, we strived to develop a decellularized human cornea to use as a scaffold for reconstructing the corneal epithelium and anterior stroma. Human cadaver corneas were decellularized by five different methods, including detergent- and nondetergent-based approaches. The success of each method on the removal of cells from the cornea was investigated. The structural integrity of decellularized corneas was compared with the native cornea by electron microscopy. The integrity of the basement membrane of the epithelium was analyzed by histology and by the expression of collagen type IV, laminin, and fibronectin. Finally, the ability of the decellularized corneas to support the growth of human corneal epithelial cells and fibroblasts was assessed in vitro. Corneas processed using Triton X-100, liquid nitrogen, and poly(ethylene glycol) resulted in incomplete removal of cellular material. Corneas processed with the use of sodium dodecyl sulfate (SDS) or with sodium chloride (NaCl) plus nucleases successfully removed all cellular material; however, only the NaCl plus nuclease treatment kept the epithelial basement membrane completely intact. Corneas processed with NaCl plus nuclease supported both fibroblast and epithelial cell growth in vitro, while corneas treated with SDS supported the growth of only fibroblasts and not epithelial cells. Decellularized human corneas provide a scaffold that can support the growth of corneal epithelial cells and stromal fibroblasts. This approach may be useful for reconstructing the anterior cornea and limbus using autologous cells.