Reacquisition of New Meristematic Sites Determines the Development of a New Organ, the Cecidomyiidae Gall on Copaifera langsdorffii Desf. (Fabaceae)
The development of gall shapes has been attributed to the feeding behavior of the galling insects and how the host tissues react to galling stimuli, which ultimately culminate in a variable set of structural responses. A superhost of galling herbivores, , hosts a bizarre "horn-shaped" leaf...
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| Published in | Frontiers in plant science Vol. 8; p. 1622 |
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| Main Authors | , , , |
| Format | Journal Article |
| Language | English |
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27.09.2017
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| Abstract | The development of gall shapes has been attributed to the feeding behavior of the galling insects and how the host tissues react to galling stimuli, which ultimately culminate in a variable set of structural responses. A superhost of galling herbivores,
, hosts a bizarre "horn-shaped" leaflet gall morphotype induced by an unidentified species of Diptera: Cecidomyiidae. By studying the development of this gall morphotype under the anatomical and physiological perspectives, we demonstrate the symptoms of the Cecidomyiidae manipulation over plant tissues, toward the cell redifferentiation and tissue neoformation. The most prominent feature of this gall is the shifting in shape from growth and development phase toward maturation, which imply in metabolites accumulation detected by histochemical tests in meristem-like group of cells within gall structure. We hypothesize that the development of complex galls, such as the horn-shaped demands the reacquisition of cell meristematic competence. Also, as mature galls are green, their photosynthetic activity should be sufficient for their oxygenation, thus compensating the low gas diffusion through the compacted gall parenchyma. We currently conclude that the galling Cecidomyiidae triggers the establishment of new sites of meristematic tissues, which are ultimately responsible for shifting from the young conical to the mature horn-shaped gall morphotype. Accordingly, the conservative photosynthesis activity in gall site maintains tissue homeostasis by avoiding hypoxia and hipercarbia in the highly compacted gall tissues. |
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| AbstractList | The development of gall shapes has been attributed to the feeding behavior of the galling insects and how the host tissues react to galling stimuli, which ultimately culminate in a variable set of structural responses. A superhost of galling herbivores,
, hosts a bizarre "horn-shaped" leaflet gall morphotype induced by an unidentified species of Diptera: Cecidomyiidae. By studying the development of this gall morphotype under the anatomical and physiological perspectives, we demonstrate the symptoms of the Cecidomyiidae manipulation over plant tissues, toward the cell redifferentiation and tissue neoformation. The most prominent feature of this gall is the shifting in shape from growth and development phase toward maturation, which imply in metabolites accumulation detected by histochemical tests in meristem-like group of cells within gall structure. We hypothesize that the development of complex galls, such as the horn-shaped demands the reacquisition of cell meristematic competence. Also, as mature galls are green, their photosynthetic activity should be sufficient for their oxygenation, thus compensating the low gas diffusion through the compacted gall parenchyma. We currently conclude that the galling Cecidomyiidae triggers the establishment of new sites of meristematic tissues, which are ultimately responsible for shifting from the young conical to the mature horn-shaped gall morphotype. Accordingly, the conservative photosynthesis activity in gall site maintains tissue homeostasis by avoiding hypoxia and hipercarbia in the highly compacted gall tissues. The development of gall shapes has been attributed to the feeding behavior of the galling insects and how the host tissues react to galling stimuli, which ultimately culminate in a variable set of structural responses. A superhost of galling herbivores, Copaifera langsdorffii, hosts a bizarre "horn-shaped" leaflet gall morphotype induced by an unidentified species of Diptera: Cecidomyiidae. By studying the development of this gall morphotype under the anatomical and physiological perspectives, we demonstrate the symptoms of the Cecidomyiidae manipulation over plant tissues, toward the cell redifferentiation and tissue neoformation. The most prominent feature of this gall is the shifting in shape from growth and development phase toward maturation, which imply in metabolites accumulation detected by histochemical tests in meristem-like group of cells within gall structure. We hypothesize that the development of complex galls, such as the horn-shaped demands the reacquisition of cell meristematic competence. Also, as mature galls are green, their photosynthetic activity should be sufficient for their oxygenation, thus compensating the low gas diffusion through the compacted gall parenchyma. We currently conclude that the galling Cecidomyiidae triggers the establishment of new sites of meristematic tissues, which are ultimately responsible for shifting from the young conical to the mature horn-shaped gall morphotype. Accordingly, the conservative photosynthesis activity in gall site maintains tissue homeostasis by avoiding hypoxia and hipercarbia in the highly compacted gall tissues.The development of gall shapes has been attributed to the feeding behavior of the galling insects and how the host tissues react to galling stimuli, which ultimately culminate in a variable set of structural responses. A superhost of galling herbivores, Copaifera langsdorffii, hosts a bizarre "horn-shaped" leaflet gall morphotype induced by an unidentified species of Diptera: Cecidomyiidae. By studying the development of this gall morphotype under the anatomical and physiological perspectives, we demonstrate the symptoms of the Cecidomyiidae manipulation over plant tissues, toward the cell redifferentiation and tissue neoformation. The most prominent feature of this gall is the shifting in shape from growth and development phase toward maturation, which imply in metabolites accumulation detected by histochemical tests in meristem-like group of cells within gall structure. We hypothesize that the development of complex galls, such as the horn-shaped demands the reacquisition of cell meristematic competence. Also, as mature galls are green, their photosynthetic activity should be sufficient for their oxygenation, thus compensating the low gas diffusion through the compacted gall parenchyma. We currently conclude that the galling Cecidomyiidae triggers the establishment of new sites of meristematic tissues, which are ultimately responsible for shifting from the young conical to the mature horn-shaped gall morphotype. Accordingly, the conservative photosynthesis activity in gall site maintains tissue homeostasis by avoiding hypoxia and hipercarbia in the highly compacted gall tissues. The development of gall shapes has been attributed to the feeding behavior of the galling insects and how the host tissues react to galling stimuli, which ultimately culminate in a variable set of structural responses. A superhost of galling herbivores, Copaifera langsdorffii, hosts a bizarre “horn-shaped” leaflet gall morphotype induced by an unidentified species of Diptera: Cecidomyiidae. By studying the development of this gall morphotype under the anatomical and physiological perspectives, we demonstrate the symptoms of the Cecidomyiidae manipulation over plant tissues, toward the cell redifferentiation and tissue neoformation. The most prominent feature of this gall is the shifting in shape from growth and development phase toward maturation, which imply in metabolites accumulation detected by histochemical tests in meristem-like group of cells within gall structure. We hypothesize that the development of complex galls, such as the horn-shaped demands the reacquisition of cell meristematic competence. Also, as mature galls are green, their photosynthetic activity should be sufficient for their oxygenation, thus compensating the low gas diffusion through the compacted gall parenchyma. We currently conclude that the galling Cecidomyiidae triggers the establishment of new sites of meristematic tissues, which are ultimately responsible for shifting from the young conical to the mature horn-shaped gall morphotype. Accordingly, the conservative photosynthesis activity in gall site maintains tissue homeostasis by avoiding hypoxia and hipercarbia in the highly compacted gall tissues. The development of gall shapes has been attributed to the feeding behavior of the galling insects and how the host tissues react to galling stimuli, which ultimately culminate in a variable set of structural responses. A superhost of galling herbivores, Copaifera langsdorffii , hosts a bizarre “horn-shaped” leaflet gall morphotype induced by an unidentified species of Diptera: Cecidomyiidae. By studying the development of this gall morphotype under the anatomical and physiological perspectives, we demonstrate the symptoms of the Cecidomyiidae manipulation over plant tissues, toward the cell redifferentiation and tissue neoformation. The most prominent feature of this gall is the shifting in shape from growth and development phase toward maturation, which imply in metabolites accumulation detected by histochemical tests in meristem-like group of cells within gall structure. We hypothesize that the development of complex galls, such as the horn-shaped demands the reacquisition of cell meristematic competence. Also, as mature galls are green, their photosynthetic activity should be sufficient for their oxygenation, thus compensating the low gas diffusion through the compacted gall parenchyma. We currently conclude that the galling Cecidomyiidae triggers the establishment of new sites of meristematic tissues, which are ultimately responsible for shifting from the young conical to the mature horn-shaped gall morphotype. Accordingly, the conservative photosynthesis activity in gall site maintains tissue homeostasis by avoiding hypoxia and hipercarbia in the highly compacted gall tissues. |
| Author | Carneiro, Renê G. S. Isaias, Rosy M. S. Oliveira, Denis C. Moreira, Ana S. F. P. |
| AuthorAffiliation | 2 Laboratório de Anatomia Vegetal, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais , Belo Horizonte , Brazil 4 Laboratório de Anatomia e Desenvolvimento Vegetal e Interações, Instituto de Biologia, Universidade Federal de Uberlândia , Uberlândia , Brazil 1 Laboratório de Anatomia Vegetal, Instituto de Ciências Biológicas, Universidade Federal de Goiás , Goiânia , Brazil 3 Laboratório de Fisiologia Vegetal, Instituto de Biologia, Universidade Federal de Uberlândia , Uberlândia , Brazil |
| AuthorAffiliation_xml | – name: 1 Laboratório de Anatomia Vegetal, Instituto de Ciências Biológicas, Universidade Federal de Goiás , Goiânia , Brazil – name: 4 Laboratório de Anatomia e Desenvolvimento Vegetal e Interações, Instituto de Biologia, Universidade Federal de Uberlândia , Uberlândia , Brazil – name: 2 Laboratório de Anatomia Vegetal, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais , Belo Horizonte , Brazil – name: 3 Laboratório de Fisiologia Vegetal, Instituto de Biologia, Universidade Federal de Uberlândia , Uberlândia , Brazil |
| Author_xml | – sequence: 1 givenname: Renê G. S. surname: Carneiro fullname: Carneiro, Renê G. S. – sequence: 2 givenname: Rosy M. S. surname: Isaias fullname: Isaias, Rosy M. S. – sequence: 3 givenname: Ana S. F. P. surname: Moreira fullname: Moreira, Ana S. F. P. – sequence: 4 givenname: Denis C. surname: Oliveira fullname: Oliveira, Denis C. |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29033957$$D View this record in MEDLINE/PubMed |
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| Cites_doi | 10.1034/j.1600-0706.2001.950120.x 10.1007/978-3-642-73635-3 10.1016/j.sajb.2014.02.011 10.1007/s00442-012-2365-1 10.1073/pnas.0604722104 10.1093/pcp/pcn148 10.1016/j.jinsphys.2015.12.009 10.1007/s004420050503 10.1007/978-94-017-6230-4 10.3389/fpls.2017.01249 10.1016/j.bbagen.2015.03.007 10.9755/ejfa.v25i3.10970 10.5539/jps.v6n1p11 10.1139/b11-048 10.1016/j.sajb.2012.08.007 10.1016/j.sajb.2009.10.011 10.1016/j.jinsphys.2015.11.012 10.1016/j.baae.2005.07.001 10.1071/BT15106 10.1104/pp.36.5.589 10.1146/annurev.arplant.59.032607.092825 10.1080/17429145.2012.705339 10.1016/j.plantsci.2010.11.005 10.1111/j.1558-5646.1998.tb02248.x 10.1016/j.pbi.2010.08.012 10.1007/s13744-013-0115-7 10.1139/cjb-2015-0012 10.1007/978-94-017-8783-3 10.11646/zootaxa.3620.1.6 10.1371/journal.pone.0129331 10.1016/j.bse.2014.02.016 10.1093/jxb/erh145 10.1007/s00709-010-0128-6 10.1016/S0304-4165(89)80016-9 10.1146/annurev.en.33.010188.002343 10.1016/j.jinsphys.2015.07.006 10.1016/S0176-1617(86)80237-1 10.1093/jxb/23.1.152 10.1016/S1360-1385(97)89954-2 10.1007/s11103-006-0061-4 10.1007/s00709-013-0519-6 10.1016/B978-0-12-394380-4.50011-6 |
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| Copyright | Copyright © 2017 Carneiro, Isaias, Moreira and Oliveira. 2017 Carneiro, Isaias, Moreira and Oliveira |
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| Keywords | gall shape hystochemistry photosynthesis cell redifferentiation |
| Language | English |
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| Title | Reacquisition of New Meristematic Sites Determines the Development of a New Organ, the Cecidomyiidae Gall on Copaifera langsdorffii Desf. (Fabaceae) |
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