Nitrification, a key process in the global nitrogen cycle that generates nitrate through microbial activity, may enhance losses of fertilizer nitrogen by leaching and denitrification. Certain plants can suppress soil-nitrification by releasing inhibitors from roots, a phenomenon termed biological nitrification inhibition (BNI). Here, we report the discovery of an effective nitrification inhibitor in the root-exudates of the tropical forage grass Brachiaria humidicola (Rendle) Schweick. Named ''brachialactone,'' this inhibitor is a recently discovered cyclic diterpene with a unique 5-8-5-membered ring system and a ␥-lactone ring. It contributed 60 -90% of the inhibitory activity released from the roots of this tropical grass. Unlike nitrapyrin (a synthetic nitrification inhibitor), which affects only the ammonia monooxygenase (AMO) pathway, brachialactone appears to block both AMO and hydroxylamine oxidoreductase enzymatic pathways in Nitrosomonas. global warming ͉ nitrogen pollution ͉ nitrous oxide emissions ͉ root exudation ͉ climate change M ost modern agricultural systems are based on large inputs of inorganic nitrogen (N), with ammonium (NH 4 ϩ ) being the primary N source (1, 2). Also, current crop management practices result in the development of highly nitrifying soil environments (3, 4). Nitrification results in the transformation of the relatively immobile NH 4 ϩ to highly mobile nitrate (NO 3 Ϫ ), making inorganic N susceptible to losses through leaching of NO 3 Ϫ and/or gaseous N emissions, potentially initiating a cascade of environmental and health problems (1, 2, 5, 6). Nitrous oxide (N 2 O) is one of the three major biogenic greenhouse gases contributing to global warming, produced primarily from denitrification processes in agricultural systems (5, 7). Also, assimilation of NO 3 Ϫ by plants can result in further N 2 O emissions directly from plant canopies (8). The low agronomic N-use efficiency (NUE) found in many agricultural systems is largely the result of N losses associated with nitrification (i.e., N losses from NO 3 Ϫ leaching and denitrification) (9-11). Most plants have the ability to assimilate both NH 4 ϩ and NO 3 Ϫ (12); therefore, nitrification does not need to be a dominant process in the N cycle for efficient N use.Nitrification is low in some forest and grassland soils (13-17). Since the early 1960s, some tropical grasses have been suspected of having the capacity to inhibit nitrification (18-21). However, this concept remained controversial due to the lack of direct evidence showing such inhibitory effects or the identification of specific inhibitors (22).We adopted a very sensitive bioassay using a recombinant luminescent Nitrosomonas europaea to detect biological nitrification inhibition (BNI) in plant-soil systems with the inhibitory activity of roots expressed in allylthiourea units (ATU) (23). Using this methodology, we were able to show that certain plants release nitrification inhibitors from their roots (23-26). Such BNI capacity appears to be relatively widespread among...

Wheat stem rust, caused by Puccinia graminis f. sp. tritici (Pgt), is a devastating disease that can cause severe yield losses. A previously uncharacterized Pgt race, designated Ug99, has overcome most of the widely used resistance genes and is threatening major wheat production areas. Here, we demonstrate that the Sr35 gene from Triticum monococcum is a coiled-coil, nucleotide-binding, leucine-rich repeat gene that confers near immunity to Ug99 and related races. This gene is absent in the A-genome diploid donor and in polyploid wheat but is effective when transferred from T. monococcum to polyploid wheat. The cloning of Sr35 opens the door to the use of biotechnological approaches to control this devastating disease and to analyses of the molecular interactions that define the wheat-rust pathosystem.

f. sp. () causes wheat stem rust, a devastating fungal disease. The resistance gene confers immunity against this pathogen's most virulent races, including Ug99. We used comparative whole-genome sequencing of chemically mutagenized and natural isolates to identify a fungal gene named that is required for avirulence. The gene encodes a secreted protein capable of interacting with Sr35 and triggering the immune response. We show that the origin of isolates virulent on is associated with the nonfunctionalization of the gene by the insertion of a mobile element. The discovery of provides a new tool for surveillance, identification of host susceptibility targets, and characterization of the molecular determinants of immunity in wheat.

Background: Cassava, an allotetraploid known for its remarkable tolerance to abiotic stresses is an important source of energy for humans and animals and a raw material for many industrial processes. A full-length cDNA library of cassava plants under normal, heat, drought, aluminum and post harvest physiological deterioration conditions was built; 19968 clones were sequencecharacterized using expressed sequence tags (ESTs).

Due to its favorable agronomic traits, tolerance to abiotic stresses and adverse environments, cassava is the most important source of dietary carbohydrates for 750 million people around the world, and is produced mainly by subsistence farmers in marginally agricultural land. Physiological postharvest deterioration (PPD) of cassava roots is an endogenous and complex process that restricts their storage potential to only a few days after harvest. This physiological phenomenon is one of the main constraints in cassava agriculture with an enormous impact on the cassava market chain. It is estimated that losses due to PPD in cassava production in Latin America and the Caribbean and in Asia reach 10% and 8%, respectively, whereas in Africa they reach 29%. Several years of research have been accumulating evidence to consider PPD as a wounding stress deficient process involving changes in enzymatic activity and oxidative stress. The primary symptoms, the development of dark bluish or brownish radial veins or streaks near xylem vessels of the root pith tissue, appear within 2-3 days after harvest and spread to the neighboring parenchyma tissues producing a more general browning discoloration throughout the root. Secondary post-harvest deterioration, often appears when the roots suffer moderate to severe damage at harvest and is mediated by a wide range of pathogenic microorganisms, Several strategies have been proposed to overcome the problem, but each alternative has its limitations due to the variable results, lack of objective and systematic methodology for PPD evaluation, applications not conducive for use at farmer-level, limited genetic variability or absence of genetic and biochemical information. The present review examines the socioeconomic impact of PPD, the physiological, biochemical and molecular processes occurring in the root during PPD, as well as the current and future alternatives to overcome the problem.

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BackgroundTwo opposing evolutionary constraints exert pressure on plant pathogens: one to diversify virulence factors in order to evade plant defenses, and the other to retain virulence factors critical for maintaining a compatible interaction with the plant host. To better understand how the diversified arsenals of fungal genes promote interaction with the same compatible wheat line, we performed a comparative genomic analysis of two North American isolates of Puccinia graminis f. sp. tritici (Pgt).ResultsThe patterns of inter-isolate divergence in the secreted candidate effector genes were compared with the levels of conservation and divergence of plant-pathogen gene co-expression networks (GCN) developed for each isolate. Comprative genomic analyses revealed substantial level of interisolate divergence in effector gene complement and sequence divergence. Gene Ontology (GO) analyses of the conserved and unique parts of the isolate-specific GCNs identified a number of conserved host pathways targeted by both isolates. Interestingly, the degree of inter-isolate sub-network conservation varied widely for the different host pathways and was positively associated with the proportion of conserved effector candidates associated with each sub-network. While different Pgt isolates tended to exploit similar wheat pathways for infection, the mode of plant-pathogen interaction varied for different pathways with some pathways being associated with the conserved set of effectors and others being linked with the diverged or isolate-specific effectors.ConclusionsOur data suggest that at the intra-species level pathogen populations likely maintain divergent sets of effectors capable of targeting the same plant host pathways. This functional redundancy may play an important role in the dynamic of the “arms-race” between host and pathogen serving as the basis for diverse virulence strategies and creating conditions where mutations in certain effector groups will not have a major effect on the pathogen’s ability to infect the host.Electronic supplementary materialThe online version of this article (doi:10.1186/s12864-017-3678-6) contains supplementary material, which is available to authorized users.

Downy mildews affect important crops and cause severe losses in production worldwide. Accurate identification and monitoring of these plant pathogens, especially at early stages of the disease, is fundamental in achieving effective disease control. The rapid development of molecular methods for diagnosis has provided more specific, fast, reliable, sensitive, and portable alternatives for plant pathogen detection and quantification than traditional approaches. In this review, we provide information on the use of molecular markers, serological techniques, and nucleic acid amplification technologies for downy mildew diagnosis, highlighting the benefits and disadvantages of the technologies and target selection. We emphasize the importance of incorporating information on pathogen variability in virulence and fungicide resistance for disease management and how the development and application of diagnostic assays based on standard and promising technologies, including high-throughput sequencing and genomics, are revolutionizing the development of species-specific assays suitable for in-field diagnosis. Our review provides an overview of molecular detection technologies and a practical guide for selecting the best approaches for diagnosis.