Arbuscular Mycorrhizal Fungi Alleviate Drought Stress in Trifoliate Orange by Regulating H+-ATPase Activity and Gene Expression
Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic-ecollection
Typ dokumentu časopisecké články
PubMed
33841484
PubMed Central
PMC8027329
DOI
10.3389/fpls.2021.659694
Knihovny.cz E-zdroje
- Klíčová slova
- H+-ATPase, citrus, mycorrhiza, proton pump, water deficit,
- Publikační typ
- časopisecké články MeSH
A feature of arbuscular mycorrhiza is enhanced drought tolerance of host plants, although it is unclear whether host H+-ATPase activity and gene expression are involved in the physiological process. The present study aimed to investigate the effects of an arbuscular mycorrhizal fungus (AMF), Funneliformis mosseae, on H+-ATPase activity, and gene expression of trifoliate orange (Poncirus trifoliata) seedlings subjected to well-watered (WW) and drought stress (DS), together with the changes in leaf gas exchange, root morphology, soil pH value, and ammonium content. Soil drought treatment dramatically increased H+-ATPase activity of leaf and root, and AMF inoculation further strengthened the increased effect. A plasma membrane (PM) H+-ATPase gene of trifoliate orange, PtAHA2 (MW239123), was cloned. The PtAHA2 expression was induced by mycorrhization in leaves and roots and also up-regulated by drought treatment in leaves of AMF-inoculated seedlings and in roots of AMF- and non-AMF-inoculated seedlings. And, the induced expression of PtAHA2 under mycorrhization was more prominent under DS than under WW. Mycorrhizal plants also showed greater photosynthetic rate, stomatal conductance, intercellular CO2 concentration, and transpiration rate and better root volume and diameter than non-mycorrhizal plants under DS. AMF inoculation significantly increased leaf and root ammonium content, especially under DS, whereas it dramatically reduced soil pH value. In addition, H+-ATPase activity was significantly positively correlated with ammonium contents in leaves and roots, and root H+-ATPase activity was significantly negatively correlated with soil pH value. Our results concluded that AMF stimulated H+-ATPase activity and PtAHA2 gene expression in response to DS, which resulted in great nutrient (e.g., ammonium) uptake and root growth, as well as low soil pH microenvironment.
College of Horticulture and Gardening Yangtze University Jingzhou China
Department of Chemistry Faculty of Science University of Hradec Kralove Hradec Kralove Czechia
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Aggarwal A., Kadian N., Tanwar A., Yadav A., Gupta K. (2011). Role of arbuscular mycorrhizal fungi (AMF) in global sustainable development. DOI
Augé R. M., Toler H. D., Saxton A. M. (2015). Arbuscular mycorrhizal symbiosis alters stomatal conductance of host plants more under drought than under amply watered conditions: a meta-analysis. PubMed DOI
Chen H., Zhang Q., Cai H., Xu F. (2017). Ethylene mediates alkaline-induced rice growth inhibition by negatively regulating plasma membrane H PubMed DOI PMC
Cheng H. Q., Giri B., Wu Q. S., Zou Y. N., Kuča K. (2021). Arbuscular mycorrhizal fungi mitigate drought stress in citrus by modulating root microenvironment. DOI
Chu G., Chen T. T., Wang Z. Q., Yang J. C., Zhang J. H. (2014). Morphological and physiological traits of roots and their relationships with water productivity in water-saving and drought-resistant rice. DOI
Fernández-Lizarazo J. C., Moreno-Fonseca L. P. (2016). Mechanisms for tolerance to water-deficit stress in plants inoculated with arbuscular mycorrhizal fungi. A review. DOI
Ferrol N., Barea J. M., Azcón-Aguilar C. (2000). The plasma membrane H+-ATPase gene family in the arbuscular mycorrhizal fungus PubMed DOI
Franco J. A., Bañón S., Vicente M. M. J., Miralles J., Martínez-Sánchez J. J. (2011). Review article:root development in horticultural plants grown under abiotic stress conditions-a review. DOI
Fuglsang A. T., Guo Y., Cuin T. A., Qiu Q., Song C., Kristiansen K. A., et al. (2007). PubMed DOI PMC
Garry M., Rosewarne F., Andrew Smith D. P., Schachtman S. E. (2007). Localization of proton-atpase genes expressed in arbuscular mycorrhizal tomato plants. PubMed DOI
Gaxiola R. A., Palmgren M. G., Schumacher K. (2007). Plant proton pumps. PubMed DOI
Gianinazzi-Pearson V., Arnould C., Oufattole M., Arango M., Gianinazzi S. (2000). Differential activation of H PubMed DOI
Hadian-Deljou M., Esna-Ashari M., Mirzaie-asl A. (2020). Alleviation of salt stress and expression of stress-responsive gene through the symbiosis of arbuscular mycorrhizal fungi with sour orange seedlings. DOI
Haruta M., Burch H. L., Nelson R. B., Barrett-Wilt G., Kline K. G., Mohsin S. B., et al. (2010). Molecular characterization of mutant PubMed DOI PMC
Haruta M., Sussman M. R. (2012). The effect of a genetically reduced plasma membrane protonmotive force on vegetative growth of PubMed DOI PMC
He J. D., Zou Y. N., Wu Q. S., Kuča K. (2020). Mycorrhizas enhance drought tolerance of trifoliate orange by enhancing activities and gene expression of antioxidant enzymes. DOI
Ingrain E. A., Malamy J. E. (2010). Root system architecture in avoiding chilling-induced water stress.
Johansen A., Finlay R. D., Olsson P. A. (2010). Nitrogen metabolism of external hyphae of the arbuscular mycorrhizal fungus DOI
Krajinski F., Courty P. E., Sieh D., Franken P., Zhang H. Q., Bucher M., et al. (2014). The H PubMed DOI PMC
Liu J. L., Chen J. D., Xie K., Tian Y., Yan A. N., Liu J. J., et al. (2020). A mycorrhiza-specific H PubMed DOI
Liu J. L., Liu J. J., Chen A. Q., Ji M. J., Chen J. D., Yang X. F., et al. (2016). Analysis of tomato plasma membrane H PubMed DOI
Livak K. J., Schmittgen T. D. (2001). Analysis of relative gene expression data using real-time quantitative PCR and the 2- PubMed DOI
Mak M., Babla M., Xu S. C., O’Carrigan A., Liu X. H., Gong Y. M., et al. (2014). Leaf mesophyll K DOI
Małgorzata J., Wdowikowska A., Grażyna K. (2018). Assay of plasma membrane H PubMed DOI
Młodziñska E., Kłobus G., Christensen M. D., Fuglsang A. T. (2014). The plasma membrane H PubMed DOI
Motte H., Beeckman T. (2020). A pH antastic ammonium response. PubMed
Palmgren M. G. (2001). Plant plasma membrane H PubMed DOI
Petrasek J., Friml J. (2009). Auxin transport routes in plant development. PubMed DOI
Phillips J. M., Hayman D. S. (1970). Improved procedures for clearing roots and staining parasitic and vesicular-arbuscular mycorrhizal fungi for rapid assessment of infection. DOI
Porcel R., Ruiz-Lozano J. M. (2004). Arbuscular mycorrhizal influence on leaf water potential, solute accumulation, and oxidative stress in soybean plants subjected to drought stress. PubMed DOI
Ramos A. C., Façanha A. R., José F. (2008a). “Ion dynamics during the polarized growth ofarbuscular mycorrhizal fungi: from presymbiosis to symbiosis,” in DOI
Ramos A. C., Façanha A. R., José F. (2008b). Proton (H PubMed DOI
Ramos A. C., Martins M. A., Okorokova-Façanha A. L., Fábio L. O., Okorokov L. A., Nuno S. (2009). Arbuscular mycorrhizal fungi induce differential activation of the plasma membrane and vacuolar H PubMed DOI
Requena N., Breuninger M., Franken P., Ocón A. (2003). Symbiotic status, phosphate, and sucrose regulate the expression of two plasma membrane H PubMed DOI PMC
Staal M., De-Cnodder T., Simon D., Vandenbussche F., Vander Straeten D., Verbelen J., et al. (2011). Apoplastic alkalinization is instrumental for the inhibition of cell elongation in the PubMed DOI PMC
Sun Y. P., Unestam T., Lucas S. D., Johanson K. J., Kenne L., Finlay R. (1999). Exudation-reabsorption in a mycorrhizal fungus, the dynamic interface for interaction with soil and soil microorganisms. DOI
Tang Z. C. (1999).
Ueno K., Kinoshita T., Inoue S., Emi T., Shimazaki K. (2005). Biochemical characterization of plasma membrane H PubMed DOI
Wang Y., Noguchi K., Ono N., Inoue S., Terashima I., Kinoshita T. (2014). Overexpression of plasma membrane H PubMed DOI PMC
Wu Q. S., He J. D., Srivastava A. K., Zou Y. N., Kuča K. (2019). Mycorrhizas enhance drought tolerance of citrus by altering root fatty acid compositions and their saturation levels. PubMed DOI
Wu Q. S., Srivastava A. K., Zou Y. N. (2013). AMF-induced tolerance to drought stress in citrus: a review. DOI
Xiong Y. C., Li F. M., Zhang T., Xia C. (2007). Evolution mechanism of non-hydraulic root-to-shoot signal during the anti-drought genetic breeding of spring wheat. DOI
Yoshida S. (1991). Chilling-induced inactivation and its recovery of tonoplast H PubMed DOI PMC
Zhang F., Zou Y. N., Wu Q. S., Kuča K. (2020). Arbuscular mycorrhizas modulate root polyamine metabolism to enhance drought tolerance of trifoliate orange.
Zou Y. N., Wang P., Li C. Y., Ni Q. D., Zhang D. J., Wu Q. S. (2017). Mycorrhizal trifoliate orange has greater root adaptation of morphology and phytohormones in response to drought stress. PubMed PMC
Zou Y. N., Wu Q. S., Kuča K. (2020). Unravelling the role of arbuscular mycorrhizal fungi in mitigating the oxidative burst of plants under drought stress. PubMed DOI