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RESEARCH ARTICLE

Resistance reaction of Medicago truncatula genotypes to Fusarium oxysporum: effect of plant age, substrate and inoculation method

Nicolas Rispail A B , Moustafa Bani A and Diego Rubiales A
+ Author Affiliations
- Author Affiliations

A Institute for Sustainable Agriculture, CSIC, Alameda del Obispo s/n, Apdo. 4084, 14080 Córdoba, Spain.

B Corresponding author. Email: nrispail@ias.csic.es

Crop and Pasture Science 66(5) 506-515 https://doi.org/10.1071/CP14216
Submitted: 26 February 2014  Accepted: 27 November 2014   Published: 24 April 2015

Abstract

Fusarium wilt, caused by several formae speciales of Fusarium oxysporum, is an important disease of most crop and pasture legumes, including field pea (Pisum sativum), chickpea (Cicer arietinum), lucerne (alfalfa, Medicago sativa) and barrel medic (M. truncatula). Medicago truncatula is an important pasture legume and a model legume species. Hence, it can be used to increase our knowledge of resistance mechanisms efficient to block F. oxysporum infection if its response to the disease is characterised. We evaluated the physiological and susceptibility responses to the disease of two contrasting M. truncatula genotypes, and the effect of several cultural conditions known to affect the disease incidence, such as plant age at infection time, growth substrate and the method of inoculation. Our results indicated that the A17 accession harbours a moderate level of resistance to the disease. We also showed that the method of inoculation strongly affected development of fusarium wilt disease in this model species, whereas it was not significantly altered by plant age or the inorganic growth substrate tested. In addition, we describe a rapid change in leaf temperature after infection, which can be used as an indirect parameter to confirm fungal infection at a very early stage of the interaction.

Additional keywords: barrel medic, disease resistance, fungal pathogen, infrared imaging system, phenotyping.


References

Baird DB, Harding SA, Lane PW, Murray DA, Payne RW, Soutar DM (2002) ‘Genstat for Windows. Introduction.’ 6th edn (VSN International: Wallingford, UK)

Bani M, Rubiales D, Rispail N (2012) A detailed evaluation method to identify sources of quantitative resistance to Fusarium oxysporum f. sp. pisi race 2 within a Pisum spp. germplasm collection. Plant Pathology 61, 532–542.
A detailed evaluation method to identify sources of quantitative resistance to Fusarium oxysporum f. sp. pisi race 2 within a Pisum spp. germplasm collection.Crossref | GoogleScholarGoogle Scholar |

Bansal U, Bariana H, Wong D, Randhawa M, Wicker T, Hayden M, Keller B (2014) Molecular mapping of an adult plant stem rust resistance gene Sr56 in winter wheat cultivar Arina. Theoretical and Applied Genetics 127, 1441–1448.
Molecular mapping of an adult plant stem rust resistance gene Sr56 in winter wheat cultivar Arina.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC2cXnslejs7s%3D&md5=47c1c6e35cc257d5266d01fe6c19b46cCAS | 24794977PubMed |

Barker DG, Pfaff T, Moreau D, Groves E, Ruffel S, Lepetit M, Whitehand S, Maillet F, Nair RM, Journet EP (2006) Growing M. truncatula: choice of substrates and growth conditions. In ‘The Medicago truncatula handbook’. (Eds Mathesius U, Journet EP, Sumner LW) (The Samuel Roberts Noble Foundation: Ardmore, OK, USA)

Bayaa B, Erskine W, Hamdi A (1995) Evaluation of a wild lentil collection for resistance to vascular wilt. Genetic Resources and Crop Evolution 42, 231–235.
Evaluation of a wild lentil collection for resistance to vascular wilt.Crossref | GoogleScholarGoogle Scholar |

Ben-Yephet Y, Shtienberg D (1997) Effects of the host, the pathogen, the environment and their interactions, on Fusarium wilt in carnation. Phytoparasitica 25, 207–216.
Effects of the host, the pathogen, the environment and their interactions, on Fusarium wilt in carnation.Crossref | GoogleScholarGoogle Scholar |

Calderón R, Navas-Cortés JA, Lucena C, Zarco-Tejada PJ (2013) High-resolution airborne hyperspectral and thermal imagery for early detection of Verticillium wilt of olive using fluorescence, temperature and narrow-band spectral indexes. Remote Sensing of Environment 139, 231–245.
High-resolution airborne hyperspectral and thermal imagery for early detection of Verticillium wilt of olive using fluorescence, temperature and narrow-band spectral indexes.Crossref | GoogleScholarGoogle Scholar |

Chaerle L, Hagenbeek D, De Bruyne E, Valcke R, Van der Straeten D (2004) Thermal and chlorophyll-fluorescence imaging distinguish plant-pathogen interactions at an early stage. Plant & Cell Physiology 45, 887–896.
Thermal and chlorophyll-fluorescence imaging distinguish plant-pathogen interactions at an early stage.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXmsFeqsbg%3D&md5=6dd5b46a8c626dff50f39335a4d8bcd6CAS |

Chaerle L, Pineda M, Romero-Aranda R, Van Der Straeten D, Baron M (2006) Robotized thermal and chlorophyll fluorescence imaging of pepper mild mottle virus infection in Nicotiana benthamiana. Plant & Cell Physiology 47, 1323–1336.
Robotized thermal and chlorophyll fluorescence imaging of pepper mild mottle virus infection in Nicotiana benthamiana.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XhtFCgur%2FF&md5=76c40f3b924d6fb535b163fb3ed589d8CAS |

Chikh-Rouhou H, Gonzalez-Torres R, Maria Alvarez J, Oumouloud A (2010) Screening and morphological characterization of melons for resistance to Fusarium oxysporum f. sp. melonis race 1.2. HortScience 45, 1021–1025.

Choi HK, Kim D, Uhm T, Limpens E, Lim H, Mun JH, Kalo P, Penmetsa RV, Seres A, Kulikova O, Roe BA, Bisseling T, Kiss GB, Cook DR (2004) A sequence-based genetic map of Medicago truncatula and comparison of marker collinearity with M. sativa. Genetics 166, 1463–1502.
A sequence-based genetic map of Medicago truncatula and comparison of marker collinearity with M. sativa.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXktlCgsLg%3D&md5=00d41e75f931ee1a5671a20139a13414CAS | 15082563PubMed |

Cirulli M, Ciccarese F (1982) Factors affecting early screening of tomatoes for monogenic and polygenic resistance to Fusarium wilt. Crop Protection 1, 341–348.
Factors affecting early screening of tomatoes for monogenic and polygenic resistance to Fusarium wilt.Crossref | GoogleScholarGoogle Scholar |

Cohen R, Burger Y, Horev C, Saar U, Raviv M (2008) Peat in the inoculation medium induces Fusarium susceptibility in melons. Plant Breeding 127, 424–428.
Peat in the inoculation medium induces Fusarium susceptibility in melons.Crossref | GoogleScholarGoogle Scholar |

Cook DR (1999) Medicago truncatula—a model in the making! Current Opinion in Plant Biology 2, 301–304.
Medicago truncatula—a model in the making!Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaK1MzptVeisA%3D%3D&md5=be8e212c949b956f6a76b879be93ae80CAS | 10459004PubMed |

Crawford EJ, Lake AWH, Boyce KG (1989) Breeding annual Medicago species for semiarid conditions in southern Australia. Advances in Agronomy 42, 399–437.

Czymmek KJ, Fogg M, Powell DH, Sweigard J, Park SY, Kang S (2007) In vivo time-lapse documentation using confocal and multi-photon microscopy reveals the mechanisms of invasion into the Arabidopsis root vascular system by Fusarium oxysporum. Fungal Genetics and Biology 44, 1011–1023.
In vivo time-lapse documentation using confocal and multi-photon microscopy reveals the mechanisms of invasion into the Arabidopsis root vascular system by Fusarium oxysporum.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXhtVSjsrrP&md5=62742ede150f5fcc2e81542afd1a2b80CAS | 17379550PubMed |

De Cal A, Garcia-Lepe R, Pascual S, Melgarejo P (1999) Effects of timing and method of application of Penicillium oxalicum on efficacy and duration of control of Fusarium wilt of tomato. Plant Pathology 48, 260–266.
Effects of timing and method of application of Penicillium oxalicum on efficacy and duration of control of Fusarium wilt of tomato.Crossref | GoogleScholarGoogle Scholar |

Di Pietro A, Madrid MP, Caracuel Z, Delgado-Jarana J, Roncero MIG (2003) Fusarium oxysporum: exploring the molecular arsenal of a vascular wilt fungus. Molecular Plant Pathology 4, 315–325.
Fusarium oxysporum: exploring the molecular arsenal of a vascular wilt fungus.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXot1Gitro%3D&md5=59ae6d8742193ac4f69ccf224b7df8feCAS |

Di Pietro A, Roncero MIG (1998) Cloning, expression, and role in pathogenicity of pg1 encoding the major extracellular endopolygalacturonase of the vascular wilt pathogen Fusarium oxysporum. Molecular Plant-Microbe Interactions 11, 91–98.
Cloning, expression, and role in pathogenicity of pg1 encoding the major extracellular endopolygalacturonase of the vascular wilt pathogen Fusarium oxysporum.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1cXmsFWitA%3D%3D&md5=e16d63eb6e56b6bc714fefbf59e0bdb1CAS | 9450333PubMed |

Dong X, Ling N, Wang M, Shen Q, Gup S (2012) Fusaric acid is a crucial factor in the disturbance of leaf water imbalance in Fusarium-infected banana plants. Plant Physiology and Biochemistry 60, 171–179.
Fusaric acid is a crucial factor in the disturbance of leaf water imbalance in Fusarium-infected banana plants.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38XhsVOiu7zL&md5=5331b280ba5bd92d899607b6e9aa3f82CAS | 22964424PubMed |

Fondevilla S, Carver TLW, Moreno MT, Rubiales D (2006) Macroscopical and histological characterisation of genes er1 and er2 for powdery mildew resistance in pea. European Journal of Plant Pathology 115, 309–321.
Macroscopical and histological characterisation of genes er1 and er2 for powdery mildew resistance in pea.Crossref | GoogleScholarGoogle Scholar |

Freeman S, Rodriguez RJ (1993) A rapid inoculation technique for assessing pathogenicity of Fusarium oxysporum f. sp. niveum and F.o. melonis in cucurbits. Plant Disease 77, 1198–1201.
A rapid inoculation technique for assessing pathogenicity of Fusarium oxysporum f. sp. niveum and F.o. melonis in cucurbits.Crossref | GoogleScholarGoogle Scholar |

Frugoli J, Harris J (2001) Medicago truncatula on the move! The Plant Cell 13, 458–463.
Medicago truncatula on the move!Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3MXis1aksbk%3D&md5=50ba298608b042f6b0eccad5005863f6CAS | 11251089PubMed |

Gordon TR, Martyn RD (1997) The evolutionary biology of Fusarium oxysporum. Annual Review of Phytopathology 35, 111–128.

Haglund WA (1989) A rapid method for inoculating pea seedlings with Fusarium oxysporum f. sp. pisi. Plant Disease 73, 457–458.
A rapid method for inoculating pea seedlings with Fusarium oxysporum f. sp. pisi.Crossref | GoogleScholarGoogle Scholar |

Hijano EH, Barnes DK, Frosheiser FI (1983) Inheritance of resistance to fusarium wilt in alfalfa. Crop Science 23, 31–34.

Hill MJ, Donald GE (1998) Australian temperate pasture database. (CD-ROM) CSIRO Division of Animal Production, Sydney.

Hoagland DR, Arnon DI (1950) The water-culture method for growing plants without soil. California Agricultural Experimental Station Circular V . 347. The College of Agriculture, University of California-Berkeley, CA, USA.

Infantino A, Kharrat M, Riccioni L, Coyne CJ, McPhee KE, Grunwald NJ (2006) Screening techniques and sources of resistance to root diseases in cool season food legumes. Euphytica 147, 201–221.
Screening techniques and sources of resistance to root diseases in cool season food legumes.Crossref | GoogleScholarGoogle Scholar |

Kamphuis LG, Williams AH, D’Souza NK, Pfaff T, Ellwood SR, Groves EJ, Singh KB, Oliver RP, Lichtenzveig J (2007) The Medicago truncatula reference accession A17 has an aberrant chromosomal configuration. New Phytologist 174, 299–303.
The Medicago truncatula reference accession A17 has an aberrant chromosomal configuration.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXls12ltb8%3D&md5=47f93bffd51cb8c5512be670a8d7d657CAS | 17388892PubMed |

Kraft JM, Haware MP, Jimenez-Diaz RM, Bayaa B, Harrabi M (1994) Screening techniques and sources of resistance to root rots and wilts in cool-season food legumes. Euphytica 73, 27–39.
Screening techniques and sources of resistance to root rots and wilts in cool-season food legumes.Crossref | GoogleScholarGoogle Scholar |

Latin RX, Snell SJ (1986) Comparison of methods for inoculation of muskmelon with Fusarium oxysporum f. sp. melonis. Plant Disease 70, 297–300.
Comparison of methods for inoculation of muskmelon with Fusarium oxysporum f. sp. melonis.Crossref | GoogleScholarGoogle Scholar |

Lichtenzveig J, Anderson J, Thomas G, Oliver RP, Singh KB (2006) Inoculation and growth with soil borne pathogenic fungi. In ‘The Medicago truncatula handbook’. (Eds U Mathesius, EP Journet, LW Sumner) (The Samuel Roberts Noble Foundation: Ardmore, OK, USA)

McPhee KE, Tullu A, Kraft JM, Muehlbauer FJ (1999) Resistance to Fusarium wilt race 2 in the Pisum core collection. Journal of the American Society for Horticultural Science 124, 28–31.

Melotto M, Underwood W, Koczan J, Nomura K, He SY (2006) Plant stomata function in innate immunity against bacterial invasion. Cell 126, 969–980.
Plant stomata function in innate immunity against bacterial invasion.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XpvVKiur0%3D&md5=076ea66d7969201513e816250c60f469CAS | 16959575PubMed |

Mepsted R, Flood J, Cooper RM (1995) Fusarium wilt of oil palm 2. Stunting as a mechanism to reduce water stress. Physiological and Molecular Plant Pathology 46, 373–387.
Fusarium wilt of oil palm 2. Stunting as a mechanism to reduce water stress.Crossref | GoogleScholarGoogle Scholar |

Michielse CB, Rep M (2009) Pathogen profile update: Fusarium oxysporum. Molecular Plant Pathology 10, 311–324.
Pathogen profile update: Fusarium oxysporum.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXmtVOkt7s%3D&md5=cb9c21ea0f2d605199f5deb2d846f5ddCAS | 19400835PubMed |

Mun JH, Kim DJ, Choi HK, Gish J, Debellé F, Mudge J, Denny R, Endré G, Saurat O, Dudez AM, Kiss GB, Roe B, Young ND, Cook DR (2006) Distribution of microsatellites in the genome of Medicago truncatula: a resource of genetic markers that integrate genetic and physical maps. Genetics 172, 2541–2555.
Distribution of microsatellites in the genome of Medicago truncatula: a resource of genetic markers that integrate genetic and physical maps.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XkvFOgtLw%3D&md5=01a4d13995f5c1307d0d408d14b981b6CAS | 16489220PubMed |

Mur LAJ, Simpson C, Gay A, Smith JA, Paveley N, Sánchez-Martin J, Prats E (2013) Stomatal lock-up following pathogenic challenge: source or symptom of costs of resistance in crops? Plant Pathology 62, 72–82.
Stomatal lock-up following pathogenic challenge: source or symptom of costs of resistance in crops?Crossref | GoogleScholarGoogle Scholar |

Nair R, Hughes SJ, Ellwood S, Oliver R, Green SL, Delalande M, Wen J, Oldroyd G (2006) M. truncatula stock centre. In ‘The Medicago truncatula handbook’. (Eds U Mathesius, EP Journet, LW Sumner) (The Samuel Roberts Noble Foundation: Ardmore, OK, USA)

Nyvall RF, Haglund WA (1976) Effect of plant age on severity of pea wilt caused by Fusarium oxysporum f. sp. pisi race 5. Phytopathology 66, 1093–1096.
Effect of plant age on severity of pea wilt caused by Fusarium oxysporum f. sp. pisi race 5.Crossref | GoogleScholarGoogle Scholar |

Prats E, Gay AP, Mur LAJ, Thomas BJ, Carver TLW (2006) Stomatal lock-open, a consequence of epidermal cell death, follows transient suppression of stomatal opening in barley attacked by Blumeria graminis. Journal of Experimental Botany 57, 2211–2226.
Stomatal lock-open, a consequence of epidermal cell death, follows transient suppression of stomatal opening in barley attacked by Blumeria graminis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XnvF2murc%3D&md5=708bceea96bcee67c13fe5f226f98c5aCAS | 16793847PubMed |

Prats E, Carver TLW, Gay AP, Mur LAJ (2007) Enemy at the gates: Interaction-specific stomatal responses to pathogenic challenge. Plant Signaling & Behavior 2, 275–277.
Enemy at the gates: Interaction-specific stomatal responses to pathogenic challenge.Crossref | GoogleScholarGoogle Scholar |

Ramírez-Suero M, Khanshour A, Martinez Y, Rickauer M (2010) A study on the susceptibility of the model legume plant Medicago truncatula to the soil-borne pathogen Fusarium oxysporum. European Journal of Plant Pathology 126, 517–530.
A study on the susceptibility of the model legume plant Medicago truncatula to the soil-borne pathogen Fusarium oxysporum.Crossref | GoogleScholarGoogle Scholar |

Riccioni L, Di Giambattista G, Valvassori M, Malta R, Porta-Puglia A (2003) Fungi associated with root rot of a lentil landrace from Sicily. Journal of Plant Pathology 85, 300

Rispail N, Rubiales D (2014) Identification of sources of quantitative resistance to Fusarium oxysporum f. sp. medicaginis in Medicago truncatula. Plant Disease 98, 667–673.
Identification of sources of quantitative resistance to Fusarium oxysporum f. sp. medicaginis in Medicago truncatula.Crossref | GoogleScholarGoogle Scholar |

Rispail N, Rubiales D (2015) Rapid and efficient estimation of pea resistance to the soil-borne pathogen Fusarium oxysporum by infrared imaging. Sensors 15, 3988–4000.

Rispail N, Kalo P, Kiss GB, Ellis THN, Gallardo K, Thompson RD, Prats E, Larrainzar E, Ladrera R, Gonzalez EM, Arrese-Igor C, Ferguson BJ, Gresshoff PM, Rubiales D (2010) Model legumes contribute to faba bean breeding. Field Crops Research 115, 253–269.
Model legumes contribute to faba bean breeding.Crossref | GoogleScholarGoogle Scholar |

Rubiales D, Fondevilla S, Chen W, Gentzbittel L, Higgins TJV, Castillejo MA, Singh KB, Rispail N (2015) Achievements and challenges in legume breeding for pest and disease resistance. Critical Reviews in Plant Sciences 34, 195–236.
Achievements and challenges in legume breeding for pest and disease resistance.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC2cXhvVOnsbbE&md5=a8104d2abc331481b64e1c58ae456be9CAS |

Sánchez-Martín J, Rubiales D, Prats E (2011) Resistance to powdery mildew (Blumeria graminis f. sp. avenae) in oat seedlings and adult plants. Plant Pathology 60, 846–856.
Resistance to powdery mildew (Blumeria graminis f. sp. avenae) in oat seedlings and adult plants.Crossref | GoogleScholarGoogle Scholar |

Schreuder W, Lamprecht SC, Holz G (2000) Race determination and vegetative compatibility grouping of Fusarium oxysporum f. sp. melonis from South Africa. Plant Disease 84, 231–234.
Race determination and vegetative compatibility grouping of Fusarium oxysporum f. sp. melonis from South Africa.Crossref | GoogleScholarGoogle Scholar |

Sedra MH, Besri M (1994) Evaluation of date palm resistance to bayoud disease due to Fusarium oxysporum f. sp. albedinis—Development of an efficient method for discriminating in-vitro plantlets acclimatized in the glasshouse. Agronomie 14, 467–472.
Evaluation of date palm resistance to bayoud disease due to Fusarium oxysporum f. sp. albedinis—Development of an efficient method for discriminating in-vitro plantlets acclimatized in the glasshouse.Crossref | GoogleScholarGoogle Scholar |

Sharma A, Rathour R, Plaha P, Katoch V, Khalsa GS, Patial V, Singh Y, Pathania NK (2010) Induction of fusarium wilt (Fusarium oxysporum f. sp. pisi) resistance in garden pea using induced mutagenesis and in vitro selection techniques. Euphytica 173, 345–356.

Stoll M, Schultz HR, Baecker G, Berkelmann-Loehnertz B (2008) Early pathogen detection under different water status and the assessment of spray application in vineyards through the use of thermal imagery. Precision Agriculture 9, 407–417.
Early pathogen detection under different water status and the assessment of spray application in vineyards through the use of thermal imagery.Crossref | GoogleScholarGoogle Scholar |

Swanson TA, van Gundy SD (1985) Influences of temperature and plant age on differentiation of races of Fusarium oxysporum f. sp. tracheiphilum on cowpea. Plant Disease 69, 779–781.

Wang B, Dale ML, Kochman JK (1999) Studies on a pathogenicity assay for screening cotton germplasms for resistance to Fusarium oxysporum f. sp. vasinfectum in the glasshouse. Australian Journal of Experimental Agricultural 39, 967–974.
Studies on a pathogenicity assay for screening cotton germplasms for resistance to Fusarium oxysporum f. sp. vasinfectum in the glasshouse.Crossref | GoogleScholarGoogle Scholar |

Wang M, Ling N, Dong X, Zhu Y, Shen Q, Guo S (2012) Thermographic visualization of leaf response in cucumber plants infected with the soil-borne pathogen Fusarium oxysporum f. sp. cucumerinum. Plant Physiology and Biochemistry 61, 153–161.
Thermographic visualization of leaf response in cucumber plants infected with the soil-borne pathogen Fusarium oxysporum f. sp. cucumerinum.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38XhslKru73E&md5=55e172d9fb5ef8ef54d15e04c9deeb89CAS | 23103050PubMed |

Wang M, Xiong Y, Ling N, Feng X, Zhong Z, Shen Q, Guo S (2013) Detection of the dynamic response of cucumber leaves to fusaric acid using thermal imaging. Plant Physiology and Biochemistry 66, 68–76.
Detection of the dynamic response of cucumber leaves to fusaric acid using thermal imaging.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3sXltVCrsLs%3D&md5=4de131a283d516aa2fb0fe2f24a7d6e7CAS | 23474432PubMed |

Young ND, Cannon SB, Sato S, Kim DJ, Cook DR, Town CD, Roe BA, Tabata S (2005) Sequencing the gene spaces of Medicago truncatula and Lotus japonicus. Plant Physiology 137, 1174–1181.
Sequencing the gene spaces of Medicago truncatula and Lotus japonicus.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXjslaqtbo%3D&md5=48b1800a909c121f8314d244e3ed5ad3CAS | 15824279PubMed |

Zhou XG, Everts KL (2004) Quantification of root and stem colonization of watermelon by Fusarium oxysporum f. sp. niveum and its use in evaluating resistance. Phytopathology 94, 832–841.
Quantification of root and stem colonization of watermelon by Fusarium oxysporum f. sp. niveum and its use in evaluating resistance.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BD1cjks1Sktg%3D%3D&md5=751ae36923ecae61209704e8fe1a7f51CAS | 18943103PubMed |