Determination of symbiotic nodule occupancy in the model Vicia tetrasperma using a fluorescence scanner

. 2011 Apr ; 107 (4) : 709-15. [epub] 20110124

Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid21262794

BACKGROUND: Fluorescent tagging of nodule bacteria forming symbioses with legume host plants represents a tool for vital tracking of bacteria inside the symbiotic root nodules and monitoring changes in gene activity. The constitutive expression of heterologous fluorescent proteins, such as green fluorescent protein (GFP), also allows screening for nodule occupancy by a particular strain. Imaging of the fluorescence signal on a macro-scale is associated with technical problems due to the robustness of nodule tissues and a high level of autofluorescence. SCOPE: These limitations can be reduced by the use of a model species with a fine root system, such as Vicia tetrasperma. Further increases in the sensitivity and specificity of the detection and in image resolution can be attained by the use of a fluorescence scanner. Compared with the standard CCD-type cameras, the availability of a laser source of a specified excitation wavelength decreases non-specific autofluorescence while the photomultiplier tubes in emission detection significantly increase sensitivity. The large scanning area combined with a high resolution allow us to visualize individual nodules during the scan of whole root systems. Using a fluorescence scanner with excitation wavelength of 488 nm, a band-pass specific emission channel of 532 nm and a long-pass background channel of 555 nm, it was possible to distinguish nodules occupied by a rhizobial strain marked with one copy of cycle3 GFP from nodules colonized by the wild-type strain. CONCLUSIONS: The main limitation of the current plant model and GFP with the wild-type emission peak at 409 nm is a sharp increase in root autofluorescence below 550 nm. The selectivity of the technique can be enhanced by the use of red-shifted fluorophores and the contrasting labelling of the variants, provided that the excitation (482 nm) and emission (737 nm) maxima corresponding to root chlorophyll are respected.

Zobrazit více v PubMed

Auriac MC, Timmers ACJ. Nodulation studies in the model legume Medicago truncatula: advantages of using the constitutive EF1 alpha promoter and limitations in detecting fluorescent reporter proteins in nodule tissues. Molecular Plant–Microbe Interactions. 2007;20:1040–1047. PubMed

Bohlool BB, Ladha JK, Garrity DP, George T. Biological nitrogen fixation for sustainable agriculture: a perspective. Plant and Soil. 1992;141:1–11.

Buschmann C. Variability and application of the chlorophyll fluorescence emission ratio red/far-red of leaves. Photosynthesis Research. 2007;92:261–271. PubMed

Chory J, Peto C, Feinbaum R, Pratt L, Ausubel F. Arabidopsis thaliana mutant that develops as a light-grown plant in the absence of light. Cell. 1989;58:991–999. PubMed

Chovanec P, Novák K. Visualization of nodulation gene activity on the early stages of Rhizobium leguminosarum bv. viciae symbiosis. Folia Microbiologica. 2005;50:323–331. PubMed

Chovanec P, Hovorka O, Novák K. Visualization of symbiotic tissue in intact root nodules of Vicia tetrasperma using GFP-marked Rhizobium leguminosarum bv. viciae. Folia Microbiologica. 2008;53:139–146. PubMed

Crameri A, Whitehorn EA, Tate E, Stemmer WPC. Improved green fluorescent protein by molecular evolution using DNA shuffling. Nature Biotechnology. 1995;14:315–319. PubMed

Cubitt AB, Heim R, Adams SR, Boyd AE, Gross LA, Tsien RY. Understanding, improving and using green fluorescent proteins. Trends in Biochemical Sciences. 1995;20:448–455. PubMed

Cubukcu P, Kang SS, Palmer RG. Genetic analysis of a root fluorescence mutant from Yunnan province, China. Soybean Genetics Newsletter. 2000;2000:27. Archived at http://soybase.org:8083/

Delannay X, Palmer RG. Four genes controlling root fluorescence in soybean. Crop Science. 1982;22:278–281.

Dowling DN, Broughton WJ. Competition for nodulation of legumes. Annual Review of Microbiology. 1986;40:131–157. PubMed

Duodu S, Brophy C, Connolly J, Svenning MM. Competitiveness of a native Rhizobium leguminosarum biovar trifolii strain for nodule occupancy is manifested during infection. Plant and Soil. 2009;318:117–126.

Floyd DJ, Barker RE. Change of ryegrass seedling root fluorescence expression during three generations of seed increase. Crop Science. 2002;42:905–911.

Fournier J, Timmers ACJ, Sieberer BJ, Jauneau A, Chabaud M, Barker DG. Mechanism of infection thread elongation in root hairs of Medicago truncatula and dynamic interplay with associated rhizobial colonization. Plant Physiology. 2008;148:1985–1995. PubMed PMC

Franssen HJ, Vijn I, Yang WC, Bisseling T. Developmental aspects of the Rhizobium–legume symbiosis. Plant Molecular Biology. 1992;19:89–107. PubMed

Gage DJ. Analysis of infection thread development using Gfp- and DsRed-expressing Sinorhizobium meliloti. Journal of Bacteriology. 2002;84:7042–7046. PubMed PMC

Gage DJ, Bobo T, Long SR. Use of green fluorescent protein to visualize the early events of symbiosis between Rhizobium meliloti and alfalfa (Medicago sativa) Journal of Bacteriology. 1996;178:7159–7166. PubMed PMC

Guinel FC. Getting around the legume nodule: I. The structure of the peripheral zone in four nodule types. Botany. 2009;87:1117–1138.

Guinel FC, Geil RD. A model for the development of the rhizobial and arbuscular mycorrhizal symbioses in legumes and its use to understand the roles of ethylene in the establishment of these two symbioses. Canadian Journal of Botany. 2002;80:695–720.

Handberg K, Stougaard J. Lotus japonicus, an autogamous, diploid legume species for classical and molecular genetics. Plant Journal. 1992;2:487–496.

Haynes JG, Czymmek KJ, Carlson CA, Veereshlingam H, Dickstein R, Sherrier DJ. Rapid analysis of legume root nodule development using confocal microscopy. New Phytologist. 2004;163:661–668. PubMed

Herrero M, De Lorenzo V, Timmis KN. Transposon vectors containing non-antibiotic resistance selection markers for cloning and stable chromosomal insertion of foreign genes in gram-negative bacteria. Journal of Bacteriology. 1990;172:6557–6567. PubMed PMC

Jun HK, Sarath C, Moran JF, Becana M, KIucas RV, Wagner FW. Characteristics of modified leghemoglobins isolated from soybean (Glycine max Merr.) root nodules. Plant Physiology. 1994;104:1231–1236. PubMed PMC

Lee KH, LaRue TA. Ethylene as a possible mediator of light-induced and nitrate-induced inhibition of nodulation of Pisum sativum L. cv. Sparkle. Plant Physiology. 1992;100:1334–1338. PubMed PMC

Leyva A, Palacios JN, Ruiz-Argueso T. Conserved plasmid hydrogen-uptake (hup)-specific sequences within Hup+ Rhizobium leguminosarum strains. Applied and Environmental Microbiology. 1987;53:2539–2543. PubMed PMC

Lie TA. Non-photosynthetic effects of red and far-red light on root-nodule formation by leguminous plants. Plant and Soil. 1969;30:391–404.

Limpens E, Ramos J, Franken C, et al. RNA interference in Agrobacterium rhizogenes-transformed roots of Arabidopsis and Medicago truncatula. Journal of Experimental Botany. 2004;55:983–992. PubMed

McPhee K. Variation for seedling root architecture in the core collection of pea germplasm. Crop Science. 2005;45:1758–1763.

Miller WG, Leveau JHJ, Lindow SE. Improved gfp and inaZ broad-host-range promoter-probe vectors. Molecular Plant–Microbe Interactions. 2000;13:1243–1250. PubMed

Newcomb W. A correlated light and electron microscopic study of symbiotic growth and differentiation in Pisum sativum root nodules. Canadian Journal of Botany. 1976;54:2163–2186.

Novák K, Škrdleta V, Němcová M, Lisá L. Optimization of rhizobial nod gene-inducing activity assay in pea root exudate. Folia Microbiologica. 1994;39:208–214.

Ntziachristos V, Bremer C, Weissleder R. Fluorescence imaging with near-infrared light: new technological advances that enable in vivo molecular imaging. European Radiology. 2003;13:195–208. PubMed

Quandt HJ, Pühler A, Broer I. Transgenic root nodules of Vicia hirsuta – a fast and efficient system for the study of gene expression in indeterminate-type nodules. Molecular Plant–Microbe Interactions. 1993;6:699–706.

Redmond JW, Batley M, Djordjevic MA, Innes RW, Kuempel PL, Rolfe BG. Flavones induce expression of nodulation genes in Rhizobium. Nature. 1986;323:632–635.

Sawada S, Palmer RG. Genetic analyses of nonfluorescent root mutants induced by mutagenesis in soybean. Crop Science. 1987;27:62–65.

Sharma SB, Signer ER. Temporal and spatial regulation of the symbiotic genes of Rhizobium meliloti in planta revealed by transposon Tn5-gusA. Genes and Development. 1990;4:344–356. PubMed

Spaink HP. Root nodulation and infection factors produced by rhizobial bacteria. Annual Review of Microbiology. 2000;54:257–288. PubMed

Sprent JI. Evolution and diversity of legume symbiosis. In: Dilworth MJ, James EK, Sprent JI, Newton WE, editors. Nitrogen-fixing leguminous symbioses. Dordrecht: Springer; 2008. pp. 1–21.

Stuurman N, Bras CP, Schlaman HRM, Wijfjes AHM, Bloemberg G, Spaink HP. Use of green fluorescent protein color variants expressed on stable broad-host-range vectors to visualize rhizobia interacting with plants. Molecular Plant–Microbe Interactions. 2000;13:1163–1169. PubMed

Svenning MM, Gudmundsson J, Fagerli IL, Leinonen P. Competition for nodule occupancy between introduced strains of Rhizobium leguminosarum biovar trifolii and its influence on plant production. Annals of Botany. 2001;88:781–787.

Van Brussel AAN, Tak T, Wetselaar A, Pees E, Wijffelman CA. Small Leguminosae as test plants for nodulation of Rhizobium leguminosarum and other rhizobia and agrobacteria harboring a leguminosarum Sym-plasmid. Plant Science Letters. 1982;27:317–325.

Vijn I, Christiansen H, Lauridsen P, et al. A 200 bp region of the pea ENOD12 promoter is sufficient for nodule-specific and Nod factor-induced expression. Plant Molecular Biology. 1995;28:1103–1110. PubMed

Vincent JM, Humphrey B, Škrdleta V. Group antigens in slow-growing rhizobia. Archiv für Mikrobiologie. 1973;89:79–82.

Wang K, Kang L, Anand A, Lazarovits G, Mysore KS. Monitoring in planta bacterial infection at both cellular and whole-plant levels using the green fluorescent protein variant GFPuv. New Phytologist. 2007;174:212–223. PubMed

Willems A. The taxonomy of rhizobia: an overview. Plant and Soil. 2006;287:3–14.

Wilson KJ. Molecular techniques for the study of rhizobial ecology in the field. Soil Biology and Biochemistry. 1995;27:501–514.

Xi C, Dirix G, Hofkens J, De Schryver FC, Vanderleyden J, Michiels J. Use of dual marker transposons to identify new symbiosis genes in Rhizobium. Microbial Ecology. 2001;41:325–332. PubMed

Xi C, Lambrecht M, Vanderleyden J, Michiels J. Bi-functional gfp- and gusA- containing mini-Tn5 transposon derivatives for combined gene expression and bacterial localization studies. Journal of Microbiological Methods. 1999;35:85–92. PubMed

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...