Experience shapes chandelier cell function and structure in the visual cortex

Detailed characterization of interneuron types in primary visual cortex (V1) has greatly contributed to understanding visual perception, yet the role of chandelier cells (ChCs) in visual processing remains poorly characterized. Using viral tracing we found that V1 ChCs predominantly receive monosynaptic input from local layer 5 pyramidal cells and higher-order cortical regions. Two-photon calcium imaging and convolutional neural network modeling revealed that ChCs are visually responsive but weakly selective for stimulus content. In mice running in a virtual tunnel, ChCs respond strongly to events known to elicit arousal, including locomotion and visuomotor mismatch. Repeated exposure of the mice to the virtual tunnel was accompanied by reduced visual responses of ChCs and structural plasticity of ChC boutons and axon initial segment length. Finally, ChCs only weakly inhibited pyramidal cells. These findings suggest that ChCs provide an arousal-related signal to layer 2/3 pyramidal cells that may modulate their activity and/or gate plasticity of their axon initial segments during behaviorally relevant events.</p

Identification of quantitative trait loci associated with maize resistance to bacterial leaf streak

Bacterial leaf streak (BLS), a foliar disease of maize (Zea mays L.) caused by Xanthomonas vasicola pv. vasculorum, recently emerged in the Americas as a disease of major importance. Little is known about the disease cycle, and consequently, management is difficult. No chemical control is available. Host resistance will likely play a major role in controlling the disease, but to date, no data regarding the resistance of maize germplasm to X. vasicola pv. vasculorum have been published. The objective of this study was to examine the genetic architecture of resistance to BLS. We conducted quantitative trait locus (QTL) mapping for BLS resistance in three maize populations: the Z022 (B73 × Oh43 recombinant inbred line) nested association mapping (NAM) population, the Z023 (B73 × Oh7B recombinant inbred line) NAM population, and the DRIL78 (NC344 × Oh7B chromosome segment substitution line) population. A total of five QTL were detected across two of the mapping populations. Of the QTL detected, one conferred a moderate effect, whereas the others conferred small effects. We also examined the relationship between resistance to BLS and resistance to three foliar diseases of maize, which had been mapped previously. The only significant correlation we found for BLS was with northern corn leaf blight [caused by Exserohilum turcicum (Pass.) K. J. Leonard & Suggs] in one of the populations, although two of the five BLS regions were involved in resistance to other diseases. These data will be useful for developing maize varieties resistant to BLS to mitigate the impact of bacterial leaf streak on maize production.This is a manuscript of an article published as Qiu, Yuting, Christopher Kaiser, Clarice Schmidt, Kirk Broders, Alison E. Robertson, and Tiffany M. Jamann. "Identification of quantitative trait loci associated with maize resistance to bacterial leaf streak." Crop Science 60, no. 1 (2020): 226-237. doi:10.1002/csc2.20099. Posted with permission.</p

Tar Spot: An Understudied Disease Threatening Corn Production in the Americas

Tar spot of corn has been a major foliar disease in several Latin American countries since 1904. In 2015, tar spot was first documented in the United States and has led to yield losses of approximately 4.5 million t annually. Tar spot is caused by an obligate pathogen, Phyllachora maydis, and thus requires a living host to grow and reproduce. Due to its obligate nature, biological and epidemiological studies are limited and impact of disease in corn production has been understudied. Here we present the current literature and gaps in knowledge of tar spot of corn in the Americas, its etiology, distribution, impact and management strategies as a resource for understanding the pathosystem. This review is intended to guide current and future research and aid in the development of more effective management strategies for this disease.This is a manuscript of an article published as Valle-Torres, J., T. J. Ross, D. Plewa, M. C. Avellaneda, J. Check, M. I. Chilvers, A. P. Cruz et al. "Tar spot: An understudied disease threatening corn production in the Americas." Plant disease 104, no. 10 (2020): 2541-2550. doi:10.1094/PDIS-02-20-0449-FE. Posted with permission

SNP markers tightly linked to root knot nematode resistance in grapevine (<i>Vitis cinerea</i>) identified by a genotyping-by-sequencing approach followed by Sequenom MassARRAY validation

<div><p>Plant parasitic nematodes, including root knot nematode <i>Meloidogyne</i> species, cause extensive damage to agriculture and horticultural crops. As <i>Vitis vinifera</i> cultivars are susceptible to root knot nematode parasitism, rootstocks resistant to these soil pests provide a sustainable approach to maintain grapevine production. Currently, most of the commercially available root knot nematode resistant rootstocks are highly vigorous and take up excess potassium, which reduces wine quality. As a result, there is a pressing need to breed new root knot nematode resistant rootstocks, which have no impact on wine quality. To develop molecular markers that predict root knot nematode resistance for marker assisted breeding, a genetic approach was employed to identify a root knot nematode resistance locus in grapevine. To this end, a <i>Meloidogyne javanica</i> resistant <i>Vitis cinerea</i> accession was crossed to a susceptible <i>Vitis vinifera</i> cultivar Riesling and results from screening the F₁ individuals support a model that root knot nematode resistance, is conferred by a single dominant allele, referred as <i>MELOIDOGYNE JAVANICA RESISTANCE1 (MJR1)</i>. Further, <i>MJR1</i> resistance appears to be mediated by a hypersensitive response that occurs in the root apical meristem. Single nucleotide polymorphisms (SNPs) were identified using genotyping-by-sequencing and results from association and genetic mapping identified the <i>MJR1</i> locus, which is located on chromosome 18 in the <i>Vitis cinerea</i> accession. Validation of the SNPs linked to the <i>MJR1</i> locus using a Sequenom MassARRAY platform found that only 50% could be validated. The validated SNPs that flank and co-segregate with the <i>MJR1</i> locus can be used for marker-assisted selection for <i>Meloidogyne javanica</i> resistance in grapevine.</p></div