Registration of ‘Purple Bounty’ and ‘Purple Prosperity’ hairy vetch

The hairy vetch (Vicia villosa Roth) cultivars ‘Purple Bounty’ (Reg. no. CV-12, PI 648342) and ‘Purple Prosperity’ (Reg. no. CV-11, PI 654047) were released in 2007 and 2008, respectively, by the USDA–ARS in collaboration with the Rodale Institute and the agricultural experiment stations of Pennsylvania State University and Cornell University. Hairy vetch is a commonly used annual legume cover crop grown for its cold tolerance, fast growth, large biomass production, and ability to fix N2. However, this species has not been selected for the traits needed to optimize its use as a cover crop. Our breeding program focused on developing a cultivar that was both early flowering and had adequate winter survival and therefore adapted to mechanical termination in organic no-till production in the U.S. Northeast and Mid-Atlantic. Purple Bounty and Purple Prosperity were developed between 1998 and 2005 using recurrent selection at nurseries in Beltsville and Keedysville, MD. In 2005–2006, selections were evaluated against commercial checks for flowering time in Maryland and Pennsylvania, and in the 2006–2007 and 2007–2008 seasons they were evaluated in 10 locations (12 total site-years) across the United States for winter survival. Purple Bounty and Purple Prosperity both flowered earlier than the commercial material against which they were tested (significance depended on the date and site); Purple Bounty was the earlier flowering of the two cultivars. Purple Bounty and Purple Prosperity also had equivalent or improved winter survival compared with ‘AU Early Cover’, an early-maturing cultivar developed in the southern United States, at all test locations. Purple Prosperity is no longer commercially available, but Purple Bounty is currently licensed and distributed by Allied Seed (Nampa, ID)

Complete genome sequence of the biocontrol agent Serratia marcescens strain N4–5 uncovers an assembly artefact

Serratia marcescens are gram-negative bacteria found in several environmental niches, including the plant rhizosphere and patients in hospitals. Here, we present the genome of Serratia marcescens strain N4–5 (=NRRL B-65519), which has a size of 5,074,473 bp (664-fold coverage) and contains 4840 protein coding genes, 21 RNA genes, and an average G + C content of 59.7%. N4–5 harbours a plasmid of 11,089 bp and 43.5% G + C content that encodes six unique CDS repeated 2.5× times totalling 13 CDS. Our genome assembly and manual curation uncovered the insertion of two extra copies of the 5S rRNA gene in the assembled sequence, which was confirmed by PCR and Sanger sequencing to be a misassembly. This artefact was subsequently removed from the final assembly. The occurrence of extra copies of the 5S rRNA gene was also observed in most complete genomes of Serratia spp. deposited in public databases in our comparative analysis. These elements, which also occur naturally, can easily be confused with true genetic variation. Efforts to discover and correct assembly artefacts should be made in order to generate genome sequences that represent the biological truth underlying the studied organism. We present the genome of N4–5 and discuss genes potentially involved in biological control activity against plant pathogens and also the possible mechanisms responsible for the artefact we observed in our initial assembly. This report raises awareness about the extra copies of the 5S rRNA gene in sequenced bacterial genomes as they may represent misassemblies and therefore should be verified experimentally. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s42770-020-00382-2) contains supplementary material, which is available to authorized users

Understanding and Enhancing Soil Biological Health: The Solution for Reversing Soil Degradation

Our objective is to provide an optimistic strategy for reversing soil degradation by increasing public and private research efforts to understand the role of soil biology, particularly microbiology, on the health of our world’s soils. We begin by defining soil quality/soil health (which we consider to be interchangeable terms), characterizing healthy soil resources, and relating the significance of soil health to agroecosystems and their functions. We examine how soil biology influences soil health and how biological properties and processes contribute to sustainability of agriculture and ecosystem services. We continue by examining what can be done to manipulate soil biology to: (i) increase nutrient availability for production of high yielding, high quality crops; (ii) protect crops from pests, pathogens, weeds; and (iii) manage other factors limiting production, provision of ecosystem services, and resilience to stresses like droughts. Next we look to the future by asking what needs to be known about soil biology that is not currently recognized or fully understood and how these needs could be addressed using emerging research tools. We conclude, based on our perceptions of how new knowledge regarding soil biology will help make agriculture more sustainable and productive, by recommending research emphases that should receive first priority through enhanced public and private research in order to reverse the trajectory toward global soil degradation

The Chlamydomonas reinhardtii Organellar Genomes Respond Transcriptionally and Post-Transcriptionally to Abiotic Stimuli

The Chlamydomonas reinhardtii plastid and mitochondrial transcriptomes were surveyed for changes in RNA profiles resulting from growth in 12 culture conditions representing 8 abiotic stimuli. Organellar RNA abundance exhibited marked changes during nutrient stress and exposure to UV light, as revealed by both RNA gel blot and DNA microarray analyses. Of particular note were large increases in tufA and clpP transcript abundance during nutrient limitation. Phosphate and sulfur limitation resulted in the most global, yet opposite, effects on organellar RNA abundance, changes that were dissected further using run-on transcription assays. Removal of sulfate from the culture medium, which is known to reduce photosynthesis, resulted in 2-fold to 10-fold decreases in transcription rates, which were reflected in lower RNA abundance. The decrease in transcriptional activity was completely reversible and recovered to twice the control level after sulfate replenishment. Conversely, phosphate limitation resulted in a twofold to threefold increase in RNA abundance that was found to be a post-transcriptional effect, because it could be accounted for by increased RNA stability. This finding is consistent with the known metabolic slowdown under phosphate stress. Additionally, inhibitor studies suggested that unlike those in higher plants, Chlamydomonas chloroplasts lack a nucleus-encoded plastid RNA polymerase. The apparently single type of polymerase could contribute to the rapid and genome-wide transcriptional responses observed within the chloroplast

Phenotypic and Nodule Microbial Diversity among Crimson Clover (Trifolium incarnatum L.) Accessions

Crimson clover (Trifolium incarnatum L.) is the most common legume cover crop in the United States. Previous research found limited genetic variation for crimson clover within the National Plant Germplasm System (NPGS) collection. The aim of this study was to assess the phenotypic and nodule microbial diversity within the NPGS crimson clover collection, focusing on traits important for cover crop performance. Experiments were conducted at the Beltsville Agricultural Research Center (Maryland, USA) across three growing seasons (2012–2013, 2013–2014, 2014–2015) to evaluate 37 crimson clover accessions for six phenotypic traits: fall emergence, winter survival, flowering time, biomass per plant, nitrogen (N) content in aboveground biomass, and proportion of plant N from biological nitrogen fixation (BNF). Accession effect was significant across all six traits. Fall emergence of plant introductions (PIs) ranged from 16.0% to 70.5%, winter survival ranged from 52.8% to 82.0%, and growing degree days (GDD) to 25% maturity ranged from 1470 GDD to 1910 GDD. Biomass per plant ranged from 1.52 to 6.51 g, N content ranged from 1.87% to 2.24%, and proportion of plant N from BNF ranged from 50.2% to 85.6%. Accessions showed particularly clear differences for fall emergence and flowering time, indicating greater diversity and potential for selection in cover crop breeding programs. Fall emergence and winter survival were positively correlated, and both were negatively correlated with biomass per plant and plant N from BNF. A few promising lines performed well across multiple key traits, and are of particular interest as parents in future breeding efforts, including PIs 369045, 418900, 561943, 561944, and 655006. In 2014–2015, accessions were also assessed for nodule microbiome diversity, and 11 genera were identified across the sampled nodules. There was large variation among accessions in terms of species diversity, but this diversity was not associated with observed plant traits, and the functional implications of nodule microbiome diversity remain unclear

The Chlamydomonas reinhardtii Plastid Chromosome: Islands of Genes in a Sea of Repeats

Chlamydomonas reinhardtii is a unicellular eukaryotic alga possessing a single chloroplast that is widely used as a model system for the study of photosynthetic processes. This report analyzes the surprising structural and evolutionary features of the completely sequenced 203,395-bp plastid chromosome. The genome is divided by 21.2-kb inverted repeats into two single-copy regions of ∼80 kb and contains only 99 genes, including a full complement of tRNAs and atypical genes encoding the RNA polymerase. A remarkable feature is that >20% of the genome is repetitive DNA: the majority of intergenic regions consist of numerous classes of short dispersed repeats (SDRs), which may have structural or evolutionary significance. Among other sequenced chlorophyte plastid genomes, only that of the green alga Chlorella vulgaris appears to share this feature. The program MultiPipMaker was used to compare the genic complement of Chlamydomonas with those of other chloroplast genomes and to scan the genomes for sequence similarities and repetitive DNAs. Among the results was evidence that the SDRs were not derived from extant coding sequences, although some SDRs may have arisen from other genomic fragments. Phylogenetic reconstruction of changes in plastid genome content revealed that an accelerated rate of gene loss also characterized the Chlamydomonas/Chlorella lineage, a phenomenon that might be independent of the proliferation of SDRs. Together, our results reveal a dynamic and unusual plastid genome whose existence in a model organism will allow its features to be tested functionally

Registration of ‘Purple Bounty’ and ‘Purple Prosperity’ hairy vetch

The hairy vetch (Vicia villosa Roth) cultivars ‘Purple Bounty’ (Reg. no. CV-12, PI 648342) and ‘Purple Prosperity’ (Reg. no. CV-11, PI 654047) were released in 2007 and 2008, respectively, by the USDA–ARS in collaboration with the Rodale Institute and the agricultural experiment stations of Pennsylvania State University and Cornell University. Hairy vetch is a commonly used annual legume cover crop grown for its cold tolerance, fast growth, large biomass production, and ability to fix N2. However, this species has not been selected for the traits needed to optimize its use as a cover crop. Our breeding program focused on developing a cultivar that was both early flowering and had adequate winter survival and therefore adapted to mechanical termination in organic no-till production in the U.S. Northeast and Mid-Atlantic. Purple Bounty and Purple Prosperity were developed between 1998 and 2005 using recurrent selection at nurseries in Beltsville and Keedysville, MD. In 2005–2006, selections were evaluated against commercial checks for flowering time in Maryland and Pennsylvania, and in the 2006–2007 and 2007–2008 seasons they were evaluated in 10 locations (12 total site-years) across the United States for winter survival. Purple Bounty and Purple Prosperity both flowered earlier than the commercial material against which they were tested (significance depended on the date and site); Purple Bounty was the earlier flowering of the two cultivars. Purple Bounty and Purple Prosperity also had equivalent or improved winter survival compared with ‘AU Early Cover’, an early-maturing cultivar developed in the southern United States, at all test locations. Purple Prosperity is no longer commercially available, but Purple Bounty is currently licensed and distributed by Allied Seed (Nampa, ID)