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Verticillium dahliae is a soilborne fungal pathogen that causes disease on many economically important crops. Based on the resistance or susceptibility of differential cultivars in tomato, isolates of V. dahliae are divided into three races. Avirulence (avr) genes within the genomes of the three races have also been identified. However, the functional role of the avr gene in race 3 isolates of V. dahliae has not been characterized. In this study, bioinformatics analysis showed that VdR3e, a cysteine-rich secreted protein encoded by the gene characterizing race 3 in V. dahliae, was likely obtained by horizontal gene transfer from the fungal genus Bipolaris. We demonstrate that VdR3e causes cell death by triggering multiple defense responses. In addition, VdR3e localized at the periphery of the plant cell and triggered immunity depending on its subcellular localization and the cell membrane receptor BAK1. Furthermore, VdR3e is a virulence factor and shows differential pathogenicity in race 3-resistant and -susceptible hosts. These results suggest that VdR3e is a virulence factor that can also interact with BAK1 as a pathogen-associated molecular pattern (PAMP) to trigger immune responses. IMPORTANCE Based on the gene-for-gene model, research on the function of avirulence genes and resistance genes has had an unparalleled impact on breeding for resistance in most crops against individual pathogens. The soilborne fungal pathogen, Verticillium dahliae, is a major pathogen on many economically important crops. Currently, avr genes of the three races in V. dahliae have been identified, but the function of avr gene representing race 3 has not been described. We investigated the characteristics of VdR3e-mediated immunity and demonstrated that VdR3e acts as a PAMP to activate a variety of plant defense responses and induce plant cell death. We also demonstrated that the role of VdR3e in pathogenicity was host dependent. This is the first study to describe the immune and virulence functions of the avr gene from race 3 in V. dahliae, and we provide support for the identification of genes mediating resistance against race 3.

Endolysosomal defects in neurons are central to the pathogenesis of prion and other neurodegenerative disorders. In prion disease, prion oligomers traffic through the multivesicular body (MVB) and are routed for degradation in lysosomes or for release in exosomes, yet how prions impact proteostatic pathways is unclear. We found that prion-affected human and mouse brain showed a marked reduction in Hrs and STAM1 (ESCRT-0), which route ubiquitinated membrane proteins from early endosomes into MVBs. To determine how the reduction in ESCRT-0 impacts prion conversion and cellular toxicity in vivo, we prion-challenged conditional knockout mice (male and female) having Hrs deleted from neurons, astrocytes, or microglia. The neuronal, but not astrocytic or microglial, Hrs-depleted mice showed a shortened survival and an acceleration in synaptic derangements, including an accumulation of ubiquitinated proteins, deregulation of phosphorylated AMPA and metabotropic glutamate receptors, and profoundly altered synaptic structure, all of which occurred later in the prion-infected control mice. Finally, we found that neuronal Hrs (nHrs) depletion increased surface levels of the cellular prion protein, PrPC, which may contribute to the rapidly advancing disease through neurotoxic signaling. Taken together, the reduced Hrs in the prion-affected brain hampers ubiquitinated protein clearance at the synapse, exacerbates postsynaptic glutamate receptor deregulation, and accelerates neurodegeneration.SIGNIFICANCE STATEMENT Prion diseases are rapidly progressive neurodegenerative disorders characterized by prion aggregate spread through the central nervous system. Early disease features include ubiquitinated protein accumulation and synapse loss. Here, we investigate how prion aggregates alter ubiquitinated protein clearance pathways (ESCRT) in mouse and human prion-infected brain, discovering a marked reduction in Hrs. Using a prion-infection mouse model with neuronal Hrs (nHrs) depleted, we show that low neuronal Hrs is detrimental and markedly shortens survival time while accelerating synaptic derangements, including ubiquitinated protein accumulation, indicating that Hrs loss exacerbates prion disease progression. Additionally, Hrs depletion increases the surface distribution of prion protein (PrPC), linked to aggregate-induced neurotoxic signaling, suggesting that Hrs loss in prion disease accelerates disease through enhancing PrPC-mediated neurotoxic signaling.

Artificial vision systems pervade our daily lives as a foremost sensing apparatus in various digital technologies, from smartphones to autonomous cars and robotics. The broad range of applications for conventional vision systems requires facile adaptation under extreme and dynamic visual environments. However, these current needs have complicated individual visual components for high-quality image acquisition and processing, which indeed leads to a decline in efficiency in the overall system. Here, we review recent advancements in visual components for high-performance visual processing based on strategies of biological eyes that execute diverse imaging functionalities and sophisticated visual processes with simple and concise ocular structures. This review first covers the structures and functions of biological eyes (i.e., single-lens eyes and compound eyes), which contain micro-optic components and nanophotonic structures. After that, we focus on their inspirations in imaging optics/photonics, light-trapping and filtering components, and retinomorphic devices. We discuss the remaining challenges and notable biological structures waiting to be implemented.

Advances in nanophotonics have created numerous pathways for light–matter interactions in nanometer scale, enriched by physical and chemical mechanisms. Over the avenue, electrically tunable photonic response is highly desired for optical encryption, optical switch, and structural color display. However, the perceived obstacle, which lies in the energy-efficient tuning mechanism and/or its weak light–matter interaction, is treated as a barrier. Here, we introduce electrochromic nanopixels made of hybrid nanowires integrated with polyaniline (PANI). The device shows optical duality between two resonators: (i) surface plasmon polariton (SPP)-induced waveguide (wavelength-selective absorber) and (ii) ultrathin resonator (broadband absorber). With switching effect of between resonant modes, we achieve enhanced chromatic variation spanning from red to green and blue while operating at a sub-1-volt level, ensuring compatibility with the CMOS voltage range. This modulation is achieved by improving the light–matter interaction, effectively harnessing the intrinsic optical property transition of PANI from lossy to dielectric in response to the redox states. In our experimental approach, we successfully scaled up device fabrication to an 8-inch wafer, tailoring the nanowire array to different dimensions for optical information encryption. Demonstrating distinct chromaticity modulation, we achieve optical encryption of multiple data bits, up to 8 bits per unit cell. By capitalizing on the remarkable sensitivity to the angular dependence of the waveguiding mode, we further enhance the information capacity to an impressive 10 bits per unit cell.

Passive radiative cooling has emerged as a sustainable energy-saving solution, characterized by its energy-free operation and absence of carbon emissions. Conventional radiative coolers are designed with a skyward orientation, allowing for efficient heat dissipation to the cold heat sink. However, this design feature presents challenges when installed on vertical surfaces, as nearby objects obstruct heat release by blocking the cooler’s skyward view. Here, we introduce a directional radiative cooling glass (DRCG) designed to facilitate efficient heat dissipation through angular selective emission. The DRCG is constructed as a multilayer structure incorporating epsilon-near-zero materials, specifically Si3N4 and Al2O3, layered on an indium-tin-oxide thermal reflector. This innovative design restricts thermal emission to specific angular ranges, known as the Berreman mode. Additionally, the transparent layers enable a visible transmittance exceeding 84 %. Theoretical simulations validate the enhanced cooling performance of the DRCG, exhibiting a temperature reduction of over 1.5 °C compared with conventional glass in hot urban environments characterized by a nearby object temperature exceeding 60 °C and a sky view factor of 0.25. Furthermore, outdoor experiments demonstrate that employing the DRCG as a window enhances space-cooling performance by ∼1.5 °C. These findings underscore the potential of transparent energy-saving windows in mitigating the urban heat island effect.