Involvement of Arbuscular Mycorrhizal Symbiosis in the Distribution of Sawgrass and Cattail in Florida Everglades

被引:6
|
作者
Lin, Li [1 ]
Webb, James [1 ]
Zhang, Xing-Hai [1 ]
机构
[1] Florida Atlantic Univ, Dept Biol Sci, Boca Raton, FL 33431 USA
关键词
Cladium jamaicense; Fungi; Gene expression; Phosphate (Pi); Phosphate transporters; Typha domingensis; PHOSPHATE TRANSPORTERS; MEDICAGO-TRUNCATULA; TYPHA-DOMINGENSIS; CLADIUM-JAMAICENSE; GROWTH; FUNGI; PHOSPHORUS; MECHANISMS; EXPRESSION; DIVERSITY;
D O I
10.1007/s13157-011-0162-y
中图分类号
Q14 [生态学(生物生态学)];
学科分类号
071012 ; 0713 ;
摘要
In areas of the Florida Everglades, USA, a massive replacement of the historically predominant sawgrass by native cattail is occurring. Phosphorus enrichment due to runoff and hydrological engineering is considered a major environmental cause. As part of our investigation into the genetic and molecular mechanisms underlying this habitat shift, we examined the possible involvement of arbuscular mycorrhizal (AM) symbiosis in sawgrass and cattail. Laboratory experiments determined that sawgrass, but not cattail, was susceptible to fungal inoculation and formed AM under low phosphate (Pi) conditions. Collection of plants from four representative sites in the Everglades revealed that while all sawgrass plants formed root AM associations, no AM was detected in cattail. We identified a phosphate transporter gene of sawgrass, CjPT4, that was preferentially expressed in roots of fungal inoculated and AM plants. In contrast, cattail PT genes were steadily expressed regardless of Pi levels. Our studies demonstrate a strong possibility that ability to form AM symbiosis is a key genetic distinction between sawgrass and cattail in their adaptive response to the changing phosphorus environment. We propose a mechanistic explanation based on AM symbiosis for the distribution and competition of these two plants in the pre-industrial Pi-deficient and modern Pi-enriched Florida Everglades ecosystems.
引用
收藏
页码:263 / 272
页数:10
相关论文
共 50 条
  • [41] The importance of integration and scale in the arbuscular mycorrhizal symbiosis
    R.M. Miller
    M. Kling
    Plant and Soil, 2000, 226 : 295 - 309
  • [42] Molecular phylogeny, morphology, mycorrhizal symbiosis, and putative distribution of the arbuscular mycorrhizal fungus Epigeocarpum japonicum (Glomeraceae)
    Yamato, Masahide
    Ohmae, Muneyuki
    Orihara, Takamichi
    Kusakabe, Ryota
    Goto, Bruno Tomio
    Blaszkowski, Janusz
    MYCOSCIENCE, 2024, 65 (06) : 270 - 277
  • [43] Molecular and cellular aspects of the arbuscular mycorrhizal symbiosis
    Harrison, MJ
    ANNUAL REVIEW OF PLANT PHYSIOLOGY AND PLANT MOLECULAR BIOLOGY, 1999, 50 : 361 - 389
  • [44] Molecular and cell biology of arbuscular mycorrhizal symbiosis
    Hause, B
    Fester, T
    PLANTA, 2005, 221 (02) : 184 - 196
  • [45] ON HOST REGULATION OF THE VESICULAR ARBUSCULAR MYCORRHIZAL SYMBIOSIS
    KOIDE, RT
    LI, MG
    NEW PHYTOLOGIST, 1990, 114 (01) : 59 - 64
  • [46] Regulation of resource exchange in the arbuscular mycorrhizal symbiosis
    Walder, Florian
    van der Heijden, Marcel G. A.
    NATURE PLANTS, 2015, 1 (11)
  • [47] Arbuscular mycorrhizal symbiosis and plant aquaporin expression
    Uehlein, Norbert
    Fileschi, Kerstin
    Eckert, Martin
    Bienert, Gerd Patrick
    Bertl, Adam
    Kaldenhoff, Ralf
    PHYTOCHEMISTRY, 2007, 68 (01) : 122 - 129
  • [48] Investigating the role of arbuscular mycorrhizal effectors in the symbiosis
    Betz, R.
    Heidt, S.
    Figueira-Galan, D.
    Requena, N.
    MOLECULAR PLANT-MICROBE INTERACTIONS, 2024, 37 (05) : 124 - 124
  • [49] VA (VESICULAR-ARBUSCULAR) MYCORRHIZAL SYMBIOSIS
    LINDERMAN, RG
    ISI ATLAS OF SCIENCE-ANIMAL & PLANT SCIENCES, 1988, 1 (02): : 183 - 188
  • [50] Preference, specificity and cheating in the arbuscular mycorrhizal symbiosis
    Sanders, IR
    TRENDS IN PLANT SCIENCE, 2003, 8 (04) : 143 - 145