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1.
Plant Cell ; 29(12): 3198-3213, 2017 12.
Artículo en Inglés | MEDLINE | ID: mdl-29114015

RESUMEN

Salinity of the soil is highly detrimental to plant growth. Plants respond by a redistribution of root mass between main and lateral roots, yet the genetic machinery underlying this process is still largely unknown. Here, we describe the natural variation among 347 Arabidopsis thaliana accessions in root system architecture (RSA) and identify the traits with highest natural variation in their response to salt. Salt-induced changes in RSA were associated with 100 genetic loci using genome-wide association studies. Two candidate loci associated with lateral root development were validated and further investigated. Changes in CYP79B2 expression in salt stress positively correlated with lateral root development in accessions, and cyp79b2 cyp79b3 double mutants developed fewer and shorter lateral roots under salt stress, but not in control conditions. By contrast, high HKT1 expression in the root repressed lateral root development, which could be partially rescued by addition of potassium. The collected data and multivariate analysis of multiple RSA traits, available through the Salt_NV_Root App, capture root responses to salinity. Together, our results provide a better understanding of effective RSA remodeling responses, and the genetic components involved, for plant performance in stress conditions.


Asunto(s)
Arabidopsis/genética , Arabidopsis/fisiología , Raíces de Plantas/anatomía & histología , Raíces de Plantas/genética , Estrés Salino/genética , Adaptación Fisiológica/efectos de los fármacos , Alelos , Arabidopsis/efectos de los fármacos , Proteínas de Arabidopsis/genética , Proteínas de Arabidopsis/metabolismo , Proteínas de Transporte de Catión/genética , Proteínas de Transporte de Catión/metabolismo , Sistema Enzimático del Citocromo P-450/metabolismo , Ecotipo , Regulación de la Expresión Génica de las Plantas/efectos de los fármacos , Variación Genética , Estudio de Asociación del Genoma Completo , Raíces de Plantas/efectos de los fármacos , Raíces de Plantas/crecimiento & desarrollo , Plantas Modificadas Genéticamente , Estrés Salino/efectos de los fármacos , Cloruro de Sodio/farmacología , Simportadores/genética , Simportadores/metabolismo
2.
Plant Cell Physiol ; 60(5): 1011-1024, 2019 May 01.
Artículo en Inglés | MEDLINE | ID: mdl-30715458

RESUMEN

Western flower thrips (WFT) are a major pest on many crops, including tomato. Thrips cause yield losses, not only through feeding damage, but also by the transmission of viruses of which the Tomato Spotted Wilt Virus is the most important one. In cultivated tomato, genetic diversity is extremely low, and all commercial lines are susceptible to WFT. Several wild relatives are WFT resistant and these resistances are based on glandular trichome-derived traits. Introgression of these traits in cultivated lines did not lead to WFT resistant commercial varieties so far. In this study, we investigated WFT resistance in cultivated tomato using a F2 population derived from a cross between a WFT susceptible and a WFT resistant cultivated tomato line. We discovered that this WFT resistance is independent of glandular trichome density or trichome-derived volatile profiles and is associated with three QTLs on chromosomes 4, 5 and 10. Foliar metabolic profiles of F3 families with low and high WFT feeding damage were clearly different. We identified α-tomatine and a phenolic compound as potential defensive compounds. Their causality and interaction need further investigation. Because this study is based on cultivated tomato lines, our findings can directly be used in nowadays breeding programs.


Asunto(s)
Flores/metabolismo , Flores/parasitología , Solanum lycopersicum/metabolismo , Solanum lycopersicum/parasitología , Thysanoptera/patogenicidad , Tricomas/metabolismo , Animales , Flores/genética , Solanum lycopersicum/genética , Sitios de Carácter Cuantitativo/genética , Tricomas/genética
3.
Plant Physiol ; 166(3): 1387-402, 2014 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-25271266

RESUMEN

The plant root is the first organ to encounter salinity stress, but the effect of salinity on root system architecture (RSA) remains elusive. Both the reduction in main root (MR) elongation and the redistribution of the root mass between MRs and lateral roots (LRs) are likely to play crucial roles in water extraction efficiency and ion exclusion. To establish which RSA parameters are responsive to salt stress, we performed a detailed time course experiment in which Arabidopsis (Arabidopsis thaliana) seedlings were grown on agar plates under different salt stress conditions. We captured RSA dynamics with quadratic growth functions (root-fit) and summarized the salt-induced differences in RSA dynamics in three growth parameters: MR elongation, average LR elongation, and increase in number of LRs. In the ecotype Columbia-0 accession of Arabidopsis, salt stress affected MR elongation more severely than LR elongation and an increase in LRs, leading to a significantly altered RSA. By quantifying RSA dynamics of 31 different Arabidopsis accessions in control and mild salt stress conditions, different strategies for regulation of MR and LR meristems and root branching were revealed. Different RSA strategies partially correlated with natural variation in abscisic acid sensitivity and different Na(+)/K(+) ratios in shoots of seedlings grown under mild salt stress. Applying root-fit to describe the dynamics of RSA allowed us to uncover the natural diversity in root morphology and cluster it into four response types that otherwise would have been overlooked.


Asunto(s)
Arabidopsis/fisiología , Raíces de Plantas/fisiología , Ácido Abscísico/farmacología , Arabidopsis/efectos de los fármacos , Arabidopsis/genética , Ecotipo , Etilenos/farmacología , Raíces de Plantas/efectos de los fármacos , Raíces de Plantas/crecimiento & desarrollo , Brotes de la Planta/metabolismo , Potasio/metabolismo , Salinidad , Tolerancia a la Sal , Sales (Química)/metabolismo , Plantones/efectos de los fármacos , Plantones/metabolismo , Sodio/metabolismo
4.
Antimicrob Agents Chemother ; 56(8): 4131-9, 2012 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-22615276

RESUMEN

Emergence of drug-resistant bacteria represents a high, unmet medical need, and discovery of new antibacterials acting on new bacterial targets is strongly needed. ATP synthase has been validated as an antibacterial target in Mycobacterium tuberculosis, where its activity can be specifically blocked by the diarylquinoline TMC207. However, potency of TMC207 is restricted to mycobacteria with little or no effect on the growth of other Gram-positive or Gram-negative bacteria. Here, we identify diarylquinolines with activity against key Gram-positive pathogens, significantly extending the antibacterial spectrum of the diarylquinoline class of drugs. These compounds inhibited growth of Staphylococcus aureus in planktonic state as well as in metabolically resting bacteria grown in a biofilm culture. Furthermore, time-kill experiments showed that the selected hits are rapidly bactericidal. Drug-resistant mutations were mapped to the ATP synthase enzyme, and biochemical analysis as well as drug-target interaction studies reveal ATP synthase as a target for these compounds. Moreover, knockdown of the ATP synthase expression strongly suppressed growth of S. aureus, revealing a crucial role of this target in bacterial growth and metabolism. Our data represent a proof of principle for using the diarylquinoline class of antibacterials in key Gram-positive pathogens. Our results suggest that broadening the antibacterial spectrum for this chemical class is possible without drifting off from the target. Development of the diarylquinolines class may represent a promising strategy for combating Gram-positive pathogens.


Asunto(s)
Complejos de ATP Sintetasa/antagonistas & inhibidores , Antibacterianos/farmacología , Bacterias Grampositivas/efectos de los fármacos , Mitocondrias/efectos de los fármacos , Quinolinas/farmacología , Staphylococcus aureus/efectos de los fármacos , Complejos de ATP Sintetasa/genética , Adenosina Trifosfato/biosíntesis , Secuencia de Aminoácidos , Biopelículas/efectos de los fármacos , Línea Celular Tumoral , Farmacorresistencia Bacteriana/genética , Bacterias Grampositivas/crecimiento & desarrollo , Células HeLa , Humanos , Pruebas de Sensibilidad Microbiana , Mycobacterium tuberculosis/efectos de los fármacos , Mycobacterium tuberculosis/crecimiento & desarrollo , Quinolinas/química , Quinolinas/toxicidad , Alineación de Secuencia , Staphylococcus aureus/crecimiento & desarrollo
5.
Antimicrob Agents Chemother ; 55(11): 5354-7, 2011 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-21876062

RESUMEN

Pyrazinoic acid, the active form of the first-line antituberculosis drug pyrazinamide, decreased the proton motive force and respiratory ATP synthesis rates in subcellular mycobacterial membrane assays. Pyrazinoic acid also significantly lowered cellular ATP levels in Mycobacterium bovis BCG. These results indicate that the predominant mechanism of killing by this drug may operate by depletion of cellular ATP reserves.


Asunto(s)
Adenosina Trifosfato/biosíntesis , Antituberculosos/farmacología , Membrana Celular/efectos de los fármacos , Membrana Celular/metabolismo , Fuerza Protón-Motriz/efectos de los fármacos , Pirazinamida/análogos & derivados , Adenosina Trifosfato/metabolismo , Mycobacterium bovis/efectos de los fármacos , Mycobacterium bovis/metabolismo , Pirazinamida/farmacología
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