Stomata-mediated interactions between plants, herbivores, and the environment
Stomata play a central role in plant responses to abiotic and biotic stresses. Existing knowledge regarding the roles of stomata in plant stress is centered on abiotic stresses and plant–pathogen interactions, but how stomata influence plant–herbivore interactions remains largely unclear. Here, we s...
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Published in | Trends in plant science Vol. 27; no. 3; pp. 287 - 300 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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England
Elsevier Ltd
01.03.2022
Elsevier BV |
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Abstract | Stomata play a central role in plant responses to abiotic and biotic stresses. Existing knowledge regarding the roles of stomata in plant stress is centered on abiotic stresses and plant–pathogen interactions, but how stomata influence plant–herbivore interactions remains largely unclear. Here, we summarize the functions of stomata in plant–insect interactions and highlight recent discoveries of how herbivores manipulate plant stomata. Because stomata are linked to interrelated physiological processes in plants, herbivory-induced changes in stomatal dynamics might have cellular, organismic, and/or even community-level impacts. We summarize our current understanding of how stomata mediate plant responses to herbivory and environmental stimuli, propose how herbivores may influence these responses, and identify key knowledge gaps in plant–herbivore interactions.
Plant stomata are emerging as important mediators of interactions between plants and herbivores.Several components in the oral secretions of herbivores, such as enzymes and phytohormones, that can trigger herbivory-induced stomatal closure have been identified.Recent evidence suggests that herbivory-induced stomatal changes play important roles in mediating interactions among plants, herbivores, pathogens, and the environment. |
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AbstractList | Stomata play a central role in plant responses to abiotic and biotic stresses. Existing knowledge regarding the roles of stomata in plant stress is centered on abiotic stresses and plant–pathogen interactions, but how stomata influence plant–herbivore interactions remains largely unclear. Here, we summarize the functions of stomata in plant–insect interactions and highlight recent discoveries of how herbivores manipulate plant stomata. Because stomata are linked to interrelated physiological processes in plants, herbivory-induced changes in stomatal dynamics might have cellular, organismic, and/or even community-level impacts. We summarize our current understanding of how stomata mediate plant responses to herbivory and environmental stimuli, propose how herbivores may influence these responses, and identify key knowledge gaps in plant–herbivore interactions. Stomata play a central role in plant responses to abiotic and biotic stresses. Existing knowledge regarding the roles of stomata in plant stress is centered on abiotic stresses and plant–pathogen interactions, but how stomata influence plant–herbivore interactions remains largely unclear. Here, we summarize the functions of stomata in plant–insect interactions and highlight recent discoveries of how herbivores manipulate plant stomata. Because stomata are linked to interrelated physiological processes in plants, herbivory-induced changes in stomatal dynamics might have cellular, organismic, and/or even community-level impacts. We summarize our current understanding of how stomata mediate plant responses to herbivory and environmental stimuli, propose how herbivores may influence these responses, and identify key knowledge gaps in plant–herbivore interactions. Plant stomata are emerging as important mediators of interactions between plants and herbivores.Several components in the oral secretions of herbivores, such as enzymes and phytohormones, that can trigger herbivory-induced stomatal closure have been identified.Recent evidence suggests that herbivory-induced stomatal changes play important roles in mediating interactions among plants, herbivores, pathogens, and the environment. Stomata play a central role in plant responses to abiotic and biotic stresses. Existing knowledge regarding the roles of stomata in plant stress is centered on abiotic stresses and plant-pathogen interactions, but how stomata influence plant-herbivore interactions remains largely unclear. Here, we summarize the functions of stomata in plant-insect interactions and highlight recent discoveries of how herbivores manipulate plant stomata. Because stomata are linked to interrelated physiological processes in plants, herbivory-induced changes in stomatal dynamics might have cellular, organismic, and/or even community-level impacts. We summarize our current understanding of how stomata mediate plant responses to herbivory and environmental stimuli, propose how herbivores may influence these responses, and identify key knowledge gaps in plant-herbivore interactions.Stomata play a central role in plant responses to abiotic and biotic stresses. Existing knowledge regarding the roles of stomata in plant stress is centered on abiotic stresses and plant-pathogen interactions, but how stomata influence plant-herbivore interactions remains largely unclear. Here, we summarize the functions of stomata in plant-insect interactions and highlight recent discoveries of how herbivores manipulate plant stomata. Because stomata are linked to interrelated physiological processes in plants, herbivory-induced changes in stomatal dynamics might have cellular, organismic, and/or even community-level impacts. We summarize our current understanding of how stomata mediate plant responses to herbivory and environmental stimuli, propose how herbivores may influence these responses, and identify key knowledge gaps in plant-herbivore interactions. |
Author | Chen, Yintong Ponce, Gabriela Ali, Jared G. Felton, Gary W. Acevedo, Flor E. Lin, Po-An Lynch, Jonathan P. Anderson, Charles T. |
Author_xml | – sequence: 1 givenname: Po-An orcidid: 0000-0002-3290-1394 surname: Lin fullname: Lin, Po-An email: poanlin2@gmail.com organization: Department of Entomology, Pennsylvania State University, State College, PA, USA – sequence: 2 givenname: Yintong surname: Chen fullname: Chen, Yintong organization: Department of Biology, Pennsylvania State University, State College, PA, USA – sequence: 3 givenname: Gabriela orcidid: 0000-0001-8556-3686 surname: Ponce fullname: Ponce, Gabriela organization: Department of Entomology, Pennsylvania State University, State College, PA, USA – sequence: 4 givenname: Flor E. orcidid: 0000-0002-0946-9951 surname: Acevedo fullname: Acevedo, Flor E. organization: Department of Entomology, Pennsylvania State University, State College, PA, USA – sequence: 5 givenname: Jonathan P. orcidid: 0000-0002-7265-9790 surname: Lynch fullname: Lynch, Jonathan P. organization: Department of Plant Science, Pennsylvania State University, State College, PA, USA – sequence: 6 givenname: Charles T. surname: Anderson fullname: Anderson, Charles T. organization: Department of Biology, Pennsylvania State University, State College, PA, USA – sequence: 7 givenname: Jared G. surname: Ali fullname: Ali, Jared G. organization: Department of Entomology, Pennsylvania State University, State College, PA, USA – sequence: 8 givenname: Gary W. orcidid: 0000-0002-1076-1431 surname: Felton fullname: Felton, Gary W. organization: Department of Entomology, Pennsylvania State University, State College, PA, USA |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/34580024$$D View this record in MEDLINE/PubMed |
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37 Allegre (10.1016/j.tplants.2021.08.017_bb0035) 2007; 173 Sun (10.1016/j.tplants.2021.08.017_bb0080) 2015; 21 Paudel Timilsena (10.1016/j.tplants.2021.08.017_bb0215) 2020; 43 Detling (10.1016/j.tplants.2021.08.017_bb0540) 1979; 72 Lin (10.1016/j.tplants.2021.08.017_bb0515) 2020; 251 Fotopoulos (10.1016/j.tplants.2021.08.017_bb0685) 2008; 59 Louis (10.1016/j.tplants.2021.08.017_bb0735) 2013; 199 Hao (10.1016/j.tplants.2021.08.017_bb0460) 2012; 5 Seidl-Adams (10.1016/j.tplants.2021.08.017_bb0605) 2015; 38 Buntin (10.1016/j.tplants.2021.08.017_bb0105) 1996; 89 Scriber (10.1016/j.tplants.2021.08.017_bb0145) 1979; 60 Detling (10.1016/j.tplants.2021.08.017_bb0545) 1979; 41 Zangerl (10.1016/j.tplants.2021.08.017_bb0575) 1997; 109 Bernays (10.1016/j.tplants.2021.08.017_bb0280) 2003; 22 Mathen (10.1016/j.tplants.2021.08.017_bb0110) 1988; 97 Poston (10.1016/j.tplants.2021.08.017_bb0530) 1976; 69 DeClerck (10.1016/j.tplants.2021.08.017_bb0115) 1988; 120 Yu (10.1016/j.tplants.2021.08.017_bb0485) 2018; 43 Lim (10.1016/j.tplants.2021.08.017_bb0085) 2015; 16 Miao (10.1016/j.tplants.2021.08.017_bb0745) 2006; 18 Huot (10.1016/j.tplants.2021.08.017_bb0570) 2014; 7 Ochoa (10.1016/j.tplants.2021.08.017_bb0095) 2011; 57 Baldwin (10.1016/j.tplants.2021.08.017_bb0615) 2006; 311 Forster (10.1016/j.tplants.2021.08.017_bb0755) 2019; 48 Sances (10.1016/j.tplants.2021.08.017_bb0650) 1979; 8 Barton (10.1016/j.tplants.2021.08.017_bb0180) 2010; 91 Guimaraes (10.1016/j.tplants.2021.08.017_bb0025) 2004; 136 Sharifi (10.1016/j.tplants.2021.08.017_bb0205) 2018; 220 Afshar (10.1016/j.tplants.2021.08.017_bb0670) 2013; 59 Rivera-Vega (10.1016/j.tplants.2021.08.017_bb0665) 2018; 107 Sarker (10.1016/j.tplants.2021.08.017_bb0780) 2006; 8 Cooper (10.1016/j.tplants.2021.08.017_bb0490) 2013; 106 Niinemets (10.1016/j.tplants.2021.08.017_bb0240) 2002; 16 Merkx-Jacques (10.1016/j.tplants.2021.08.017_bb0725) 2005; 5 Afshar (10.1016/j.tplants.2021.08.017_bb0730) 2010; 56 Melotto (10.1016/j.tplants.2021.08.017_bb0030) 2006; 126 Wu (10.1016/j.tplants.2021.08.017_bb0390) 2020; 578 Showmaker (10.1016/j.tplants.2021.08.017_bb0320) 2016; 11 Hall (10.1016/j.tplants.2021.08.017_bb0525) 1976; 69 Dunn (10.1016/j.tplants.2021.08.017_bb0075) 1998; 122 |
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SubjectTerms | abiotic stress biotic stress Environmental effects guard cell Herbivores Herbivory host-pathogen relationships Insects oral secretions plant defense plant response Plant stress plant volatile plant-insect relations planting Stomata |
Title | Stomata-mediated interactions between plants, herbivores, and the environment |
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