Abstract
The genus Fusarium includes numerous toxigenic species that are pathogenic to plants or humans, and are able to colonize a wide range of environments on earth. The genus comprises around 70 well-known species, identified by using a polyphasic approach, and as many as 300 putative species, according to phylogenetic species concepts; many putative species do not yet have formal names.
Fusarium is one of the most economically important fungal genera because of yield loss due to plant pathogenic activity; mycotoxin contamination of food and feed products which often render them unaccep for marketing; and health impacts to humans and livestock, due to consumption of mycotoxins. Among the most important mycotoxins produced by species of Fusarium are the trichothecenes and the fumonisins. Fumonisins cause fatal livestock diseases and are considered potentially carcinogenic mycotoxins for humans, while trichothecenes are potent inhibitors of protein synthesis. This chapter summarizes the main aspects of morphology, pathology, and toxigenicity of the main Fusarium species that colonize different agricultural crops and environments worldwide, and cause mycotoxin contamination of food and feed.
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Desjardins AE (2006) Fusarium mycotoxins: chemistry, genetics, and biology. APS Press, St Paul, MN, 260 pp
Marasas WFO, Nelson PE, Toussoun TA (1984) Toxigenic Fusarium species: Identity and mycotoxicology. Pennsylvania State University Press, University Park, PA, 328 pp
Munkvold GP (2003) Mycotoxins in corn—occurrence, impact, and management Ch. 23 (pp. 811–881). In: White PJ, Johnson LA (eds) Corn: chemistry and technology, 2nd edn. American Association of Cereal Chemists, St. Paul, MN, 892 pp
European Food Safety Authority (2013) Deoxynivalenol in food and feed: occurrence and exposure. EFSA J 11(10):3379. doi:10.2903/j.efsa.2013.3379, 56 pp
Waskiewicz A, Beszterda M, Golinski P (2012) Occurrence of fumonisins in food—an interdisciplinary approach to the problem. Food Control 26(2):491–499
Wu F, Munkvold GP (2008) Mycotoxins in ethanol co-products: modeling economic impacts on the livestock industry and management strategies. J Agric Food Chem 56(11):3900–3911
Logrieco AF, Haidukowski M, Susca A, Mule G, Munkvold GP, Moretti A (2014) Aspergillus section Nigri as contributor of Fumonisin B2 contamination in maize. Food Addit Contam Part A Chem Anal Control Expo Risk Assess 31(1):149–155
Cuomo CA, Güldener U, Xu JR, Trail F, Turgeon BG, Di Pietro A, Walton JD et al (2007) The Fusarium graminearum genome reveals a link between localized polymorphism and pathogen specialization. Science 317:1400–1402
Gardiner DM, McDonald MC, Covarelli L, Solomon PS, Rusu AG, Marshall M, Kanzan K et al (2012) Comparative pathogenomics reveals horizontally acquired novel virulence genes in fungi infecting cereal hosts. PLoS Pathog 8(9):e1002952
Lysoe E, Harris LJ, Walkowiak S, Subramaniam R, Divon HH, Riiser ES, Llorens C et al (2014) The genome of the generalist plant pathogen Fusarium avenaceum is enriched with genes involved in redox, signaling and secondary metabolism. PLoS One 9(11):e112703
Wiemann P, Sieber CMK, Von Bargen KW, Studt L, Niehaus EM, Espino JJ, Huss K et al (2013) Deciphering the cryptic genome: genome-wide analyses of the rice pathogen Fusarium fujikuroi reveal complex regulation of secondary metabolism and novel metabolites. PLoS Pathog 9(6):e1003475
Jeong HY, Lee SH, Choi GJ, Lee T, Yun SH, Jeong HY, Lee SH, Choi GJ, Yun SH (2013) Draft genome sequence of Fusarium fujikuroi B14, the causal agent of the bakanae disease of rice. Genome Announc 1(1):e00035-13
Ma LJ, van der Does HC, Borkovich KA, Coleman JJ, Daboussi MJ, Pietro AD, Dufresne M et al (2010) Comparative genomics reveals mobile pathogenicity chromosomes in Fusarium. Nature 464:367–373
Guo L, Han L, Yang L, Zeng H, Fan D, Zhu Y, Feng Y et al (2014) Genome and transcriptome analysis of the fungal pathogen Fusarium oxysporum f. sp. cubense causing banana vascular wilt disease. PLoS One 9(4):e95543
Coleman JJ, Rounsley SD, Rodriguez-Carres M, Kuo A, Wasmann CC, Grimwood J, Schmutz J et al (2009) The genome of Nectria haematococca: contribution of supernumerary chromosomes to gene expansion. PLoS Genet 5(8):e1000618
Srivastava SK, Huang X, Brar HK, Fakhoury AM, Bluhm BH, Bhattacharyya MK (2014) The genome sequence of the fungal pathogen Fusarium virguliforme that causes sudden death syndrome in soybean. PLoS One 9:e81832
Geiser DM, Aoki T, Bacon CW, Baker SE, Bhattacharyya MK, Brandt ME, Brown DW et al (2013) One fungus, one name: defining the genus Fusarium in a scientifically robust way that preserves longstanding use. Phytopathology 103(5):400–408
O’Donnell K, Rooney AP, Proctor RH, Brown DW, McCormick SP, Ward TJ, Frandsen RJN et al (2013) Phylogenetic analyses of Rpb1 and Rpb2 strongly support a middle cretaceous origin for a clade comprising all agriculturally and medically important Fusaria. Fungal Genet Biol 52:20–31
O’Donnell K, Sutton DA, Rinaldi MG, Gueidan C, Crous PW, Geiser DM (2009) Novel multilocus sequence typing scheme reveals high genetic diversity of human pathogenic members of the Fusarium incarnatum-F. equiseti and F. chlamydosporum species complexes within the United States. J Clin Microbiol 47(12):3851–3861
Link HF (1809) Observationes in ordines plantarum naturals. Mag Ges Naturf Freunde 3:3–42
Wollenweber HW, Reinking OA (1935) Die Fusarien, ihre Beschreibung, Schadwirkung, und Bekämpfung. Paul Parey, Berlin
Snyder WC, Hansen HN (1940) The species concept in Fusarium. Am J Bot 27(2):64–67
Snyder WC, Hansen HN (1941) The species concept in Fusarium with reference to Martiella. Am J Bot 28(9):738–742
Snyder WC, Hansen HN (1945) The species concept in Fusarium with reference to Discolor and other sections. Am J Bot 32(10):657–666
Gordon WL (1952) The occurrence of Fusarium species in Canada. 2. prevalence and taxonomy of Fusarium species in cereal seed. Can J Bot 30(2):209–251
Booth C (1971) The genus Fusarium. Commonwealth Mycological Institute, Kew, Surrey
Nelson PE, Toussoun TA, Marasas WFO (1983) Fusarium species: an illustrated manual for identification (University Park. Penn State University Press, Pennsylvania
Leslie JF, Summerell BA (2006) The Fusarium laboratory manual. Blackwell, Ames, Iowa
Aoki T, O’Donnell K, Geiser DM (2014) Systematics of key phytopathogenic Fusarium species: current status and future challenges. J Gen Plant Pathol 80(3):189–201
Desjardins AE (2003) Gibberella from A (venaceae) to Z (eae). Annu Rev Phytopathol 41:177–198
Hawksworth DL (2011) A new dawn for the naming of fungi: impacts of decisions made in Melbourne in July 2011 on the future publication and regulation of fungal names. Mycokeys 1:7–20
Nelson PE, Toussoun TA, Cook RJ (1981) Fusarium: diseases, biology, and taxonomy. Pennsylvania State University Press, University Park, Pennsylvania
Covey PA, Kuwitzky B, Hanson M, Webb KM (2014) Multilocus analysis using putative fungal effectors to describe a population of Fusarium oxysporum from sugar beet. Phytopathology 104(8):886–896
WHO. Food Additives Series no. 47. (2001) Safety evaluation of certain mycotoxins in food. FAO Food and Nutrition Paper, 74, 701 pp
WHO (2002) Evaluation of certain mycotoxins in food: fifty-sixth report of the joint FAO/WHO expert committee on food additives. WHO Technical Report Series, 906, 62 pp
NTP (2001) Technical report on the toxicology and carcinogenesis studies of fumonisin B1 (CAS NO. 116355-83-0) in F344/N Rats AND B6C3F1 MICE (Feed Studies). NTP TR 496. (U.S. Dept. of Health and Human Services, NIH Publication No. 01-3955)
Alexander NJ, Proctor RH, McCormick SP (2009) Genes, gene clusters, and biosynthesis of trichothecenes and fumonisins in Fusarium. Toxin Rev 28:198–215
Kimura M, Tokai T, Takahashi-Ando N, Ohsato S, Fujimura M (2007) Molecular and genetic studies of Fusarium trichothecene biosynthesis: pathways, genes, and evolution. Biosci Biotechnol Biochem 71(9):2105–2123
McCormick SP, Stanley AM, Stover NA, Alexander NJ (2011) Trichothecenes: from simple to complex mycotoxins. Toxins 3(7):802–814
Woloshuk CP, Shim WB (2013) Aflatoxins, fumonisins, and trichothecenes: a convergence of knowledge. FEMS Microbiol Rev 37(1):94–109
Proctor RH, Van Hove F, Susca A, Stea G, Busman M, van der Lee T, Waalwijk C, Moretti A, Ward TJ (2013) Birth, death and horizontal transfer of the fumonisin biosynthetic gene cluster during the evolutionary diversification of Fusarium. Mol Microbiol 90(2):290–306
Foroud NA, Eudes F (2009) Tricothecenes in cereal grains. Int J Mol Sci 10(1):147–173
Sydenham EW, Shephard GS, Thiel PG, Marasas WFO, Stockenstrom S (1991) Fumonisin contamination of commercial corn-based human foodstuffs. J Agric Food Chem 39(11):2014–2018
Rodrigues I, Handl J, Binder EM (2011) Mycotoxin occurrence in commodities, feeds and feed ingredients sourced in the Middle East and Africa. Food Addit Contam Part B Surveill 4(3):168–179. doi:10.1080/19393210.2011.589034
Schatzmayr G, Streit E (2013) Global occurrence of mycotoxins in the food and feed chain: facts and figures. World Mycotoxin J 6(3):213–222
Wood GE (1992) Mycotoxins in foods and feeds in the United States. J Anim Sci 70(12):3941–3949
Griessler K, Rodrigues I, Handl J, Hofstetter U (2010) Occurrence of mycotoxins in Southern Europe. World Mycotoxin J 3(3):301–309
SCF (Scientific Committee for Food). Opinion of the scientific committee for food on Fusarium toxins. Part 6: Group evaluation of T-2 toxin, HT-2 Toxin, nivalenol and deoxynivalenol. http://ec.europa.eu/food/fs/sc/scf/out123_en.pdf.
EFSA Panel on Contaminants in the Food Chain (2011) Scientific opinion on the risks for animal and public health related to the presence of T-2 and HT-2 toxin in food and feed. EFSA J 9(12):2481. doi:10.2903/j.efsa.2011.2481
Jestoi M (2008) Emerging Fusarium-mycotoxins fusaproliferin, beauvericin, enniatins, and moniliformin—a review. Crit Rev Food Sci Nutr 48(1):21–49
Logrieco A, Moretti A, Castella G, Kostecki M, Golinski P, Ritieni A, Chelkowski J (1998) Beauvericin production by Fusarium species. Appl Environ Microbiol 64(8):3084–3088
Goswami RS, Kistler HC (2005) Pathogenicity and in planta mycotoxin accumulation among members of the Fusarium graminearum species complex on wheat and rice. Phytopathology 95(12):1397–1404
Toth B, Kaszonyi G, Bartok T, Varga J, Mesterhazy A (2008) Common resistance of wheat to members of the Fusarium graminearum species complex and F. culmorum. Plant Breed 127(1):1–8
Scauflaire J, Gourgue M, Callebaut A, Munaut F (2012) Fusarium temperatum, a mycotoxin-producing pathogen of maize. Eur J Plant Pathol 133(4):911–922
Moretti A, Mule G, Ritieni A, Logrieco A (2007) Further data on the production of beauvericin, enniatins and fusaproliferin and toxicity to Artemia salina by Fusarium species of Gibberella fujikuroi species complex. Int J Food Microbiol 118(2):158–163
Lattanzio VMT, von Holst C, Visconti A (2013) Experimental design for in-house validation of a screening immunoassay kit. The case of a multiplex dipstick for Fusarium mycotoxins in cereals. Anal Bioanal Chem 405(24):7773–7782
EFSA Panel on Contaminants in the Food Chain (2013) Scientific opinion on risks for animal and public health related to the presence of nivalenol in food and feed. EFSA J 11(6):3262
Rocha O, Ansari K, Doohan FM (2005) Effects of trichothecene mycotoxins on eukaryotic cells: a review. Food Addit Contam 22(4):369–378
Gerez JR, Pinto P, Callu P (2015) Deoxynivalenol alone or in combination with nivalenol and zearalenone induce systemic histological changes in pigs. Exp Toxicol Pathol 67(3):89–98
Arunachalam C, Doohan FM (2013) Trichothecene toxicity in eukaryotes: cellular and molecular mechanisms in plants and animals. Toxicol Lett 217(2):149–158
Beasley VR, Swanson SP, Corley RA, Buck WB, Koritz GD, Burmeister HR (1986) Pharmacokinetics of the trichothecene mycotoxin, T-2 toxin, in swine and cattle. Toxicon 24(1):13–23
Eriksen GS, Pettersson H (2004) Toxicological evaluation of trichothecenes in animal feed. Anim Feed Sci Technol 114:205–239
Flannery BM, Clark ES, Pestka JJ (2012) Anorexia induction by the trichothecene deoxynivalenol (vomitoxin) is mediated by the release of the gut satiety hormone peptide Yy. Toxicol Sci 130(2):289–297
Pestka JJ (2010) Deoxynivalenol: mechanisms of action, human exposure, and toxicological relevance. Arch Toxicol 84(9):663–679
World Health Organization (2011) Safety evaluation of certain contaminants in food: 72nd report of the joint FAO/WHO expert committee on food additives. World Health Organization (WHO Food Additives Series 63), Geneva
World Health Organization (WHO) (2000) Safety evaluation of certain mycotoxins in food. Fifty-third Report of the FAO/WHO Joint Expert Committee on Food Additives. WHO Technical Report Series 896, Geneva.
Pitt JI, Wild CP, Baan RA, Gelderblom WCA, Miller JD, Riley RT, Wu F (2012) Improving public health through mycotoxin control. IARC Scientific Publication 158, Geneva World Organization Press, Lyon
Yoshizawa T (1983) Red-mold diseases and natural occurrence in Japan. In: Uedo Y (ed) Trichothecenes, chemical, biological and toxicological aspects. Kodansha, Tokyo, pp 195–209
Eudes F, Comeau A, Rioux S, Collin J (2000) Phytotoxicity of eight mycotoxins associated with Fusarium in wheat head blight. Can J Plant Pathol 22(3):286–292
Proctor RH, Hohn TM, McCormick SP (1997) Restoration of wild-type virulence to Tri5 disruption mutants of Gibberella zeae via gene reversion and mutant complementation. Microbiology 143:2583–2591
Harris LJ, Desjardins AE, Plattner RD, Nicholson P, Butler G, Young JC, Weston G, Proctor RH, Hohn TM (1999) Possible role of trichothecene mycotoxins in virulence of Fusarium graminearum on maize. Plant Dis 83(10):954–960
Proctor RH, Hohn TM, McCormick SP (1995) Reduced virulence of Gibberella zeae caused by disruption of a trichothecene toxin biosynthetic gene. Mol Plant Microbe Interact 8(4):593–601
Bruns T, Wise RP, Munkvold GP (2015) Colonization of maize, wheat and soybean seedlings by mycotoxin-deficient mutants of Fusarium graminearum and F. verticillioides. 13th European Fusarium Seminar Martina Franca, Italy, p. 63
Jansen C, von Wettstein D, Schafer W, Kogel KH, Felk A, Maier FJ (2005) Infection patterns in barley and wheat spikes inoculated with wild-type and trichodiene synthase gene disrupted Fusarium graminearum. Proc Natl Acad Sci U S A 102(46):16892–16897
Bai GH, Plattner R, Desjardins A, Kolb F (2008) Resistance to Fusarium head blight and deoxynivalenol accumulation in wheat. Plant Breed 120(1):1–6
Schollenberger M, Mueller HM, Ernst K, Sondermann S, Liebscher M, Schlecker C, Wischer G et al (2012) Occurrence and distribution of 13 trichothecene toxins in naturally contaminated maize plants in Germany. Toxins 4(10):778–877
Council for Agricultural Science and Technology, CAST (2003) Mycotoxins: risks in plant and animal systems. Task Force Report No. 139, Ames, IA
Urry WH, Wehrmeister HL, Hodge EB, Hidy PH (1966) The structure of zearalenone from Gibberella zeae, Fusarium graminearum. Tetrahedron Lett 27:3109–3114
Hidy PH, Baldwin RS, Greasham RL, Keith CL, McMullen JR (1977) Zearalenone and some derivatives: production and biological activities. Adv Appl Microbiol 22:59–82
Hurd RN (1977) Structure activity relationships in zearalenones. In: Rodricks JV, Hesseltine CW, Mehlman MA (eds) Mycotoxins in human and animal health. Pathotox, Park Forest South
Hagler WM Jr, Towers NR, Mirocha CJ (2001) Zearalenone: mycotoxin or mycoestrogen? In: Summerell BA, Leslie JF, Backhouse D, Bryden WL, Burgess LW (eds) Fusarium: Paul E. Nelson memorial symposium. APS Press, St. Paul
Prelusky DB, Rotter BA, Rotter RG (1994) Toxicology of mycotoxins. In: Jd M, Trenholmes HL (eds) Mycotoxins in grain: compounds other than aflatoxin. Eagan Press, St. Paul
Zinedine A, Soriano JM, Molto JC, Manes J (2007) Review on the toxicity, occurrence, metabolism, detoxification, regulations and intake of zearalenone: an oestrogenic mycotoxin. Food Chem Toxicol 45(1):1–18
US National Toxicology Program (1982) Carcinogenesis bioassay of Zearalenone (CAS No. 17924-92-4) In F344/N Rats and B6C3F1 Mice (Feed Study). Technical report series no 235, NIH publ. No 83-1791. Research Triangle Park
Martins ML, Martins HM (2002) Influence of water activity, temperature and incubation time on the simultaneous production of deoxynivalenol and zearalenone in corn (Zea mays) by Fusarium graminearum. Food Chem 79(3):315–318
Susca A, Moretti A, Stea G, Villani A, Haidukowski M, Logrieco A, Munkvold G (2014) Comparison of species composition and fumonisin production in Aspergillus section Nigri populations in maize kernels from USA and Italy. Int J Food Microbiol 188:75–82
World Health Organization (WHO) (2000) In: Fumonisin B1. Environmental health criteria, vol 219, 150 pp
Smith GW, Constable PD, Foreman JH, Eppley RM, Waggoner AL, Tumbleson ME, Haschek WM (2002) Cardiovascular changes associated with intravenous administration of fumonisin B1 in horses. Am J Vet Res 63(4):538–545
Constable PD, Smith GW, Rottinghaus GE, Tumbleson ME, Haschek WM (2003) Fumonisin-induced blockade of ceramide synthase in sphingolipid biosynthetic pathway alters aortic input impedance spectrum of pigs. Am J Physiol Heart Circ Physiol 284(6):H2034–H2044
Marasas WFO (2001) Discovery and occurrence of the fumonisins: a historical perspective. Environ Health Perspect 109:239–243
IARC (2002) Some traditional herbal medicines, some mycotoxins, naphthalene and styrene. International Agency for Research on Cancer Monographs on the Evaluation of Carcinogenic Risks to Humans 82, IARC Press, Lyon
Desjardins AE, Plattner RD, Nelsen TC, Leslie JF (1995) Genetic-analysis of fumonisin production and virulence of Gibberella fujikuroi mating population A (Fusarium moniliforme) on maize (Zea mays) seedlings. Appl Environ Microbiol 61(1):79–86
Desjardins AE, Munkvold GP, Plattner RD, Proctor RH (2002) FUM1—a gene required for fumonisin biosynthesis but not for maize ear rot and ear infection by Gibberella moniliformis in field tests. Mol Plant Microbe Interact 15:1157–1164
Arias SL, Theumer MG, Mary VS, Rubinstein HR (2012) Fumonisins: probable role as effectors in the complex interaction of susceptible and resistant maize hybrids and Fusarium verticillioides. J Agric Food Chem 60(22):5667–5675
Glenn AE, Zitomer NC, Zimeri AM, Williams LD, Riley RT, Proctor RH (2008) Transformation-mediated complementation of a FUM gene cluster deletion in Fusarium verticillioides restores both fumonisin production and pathogenicity on maize seedlings. Mol Plant Microbe Interact 21(1):87–97
Bezuidenhout SC, Gelderblom WCA, Gorstallman CP, Horak RM, Marasas WFO, Spiteller G, Vleggaar R (1988) Structure elucidation of the fumonisins, mycotoxins from Fusarium moniliforme. J Chem Soc Chem Commun 11:743–745
Rheeder JP, Marasas WFO, Thiel PG, Sydenham EW, Shephard GS, Vanschalkwyk DJ (1992) Fusarium moniliforme and fumonisins in corn in relation to human esophageal cancer in Transkei. Phytopathology 82(3):353–357
Shephard GS, Van der Westhuizen L, Sewram V (2007) Biomarkers of exposure to fumonisin mycotoxins: a review. Food Addit Contam 24(10):1196–1201
Wang H, Wei H, Ma J, Luo X (2000) The fumonisin B1 content in corn from North China, a high-risk area of esophageal cancer. J Environ Pathol Toxicol Oncol 19:139–141
Sun G, Wang S, Hu X, Su J, Huang T, Yu J, Tang L, Gao W, Wang JS (2007) Fumonisin B1 contamination of home-grown corn in high-risk areas for esophageal and liver cancer in China. Food Addit Contam Part A Chem Anal Control Expo Risk Assess 24(2):181–185
Franceschi S, Bidoli E, Baron AE, Lavecchia C (1990) Maize and risk of cancers of the oral cavity, pharynx, and esophagus in Northeastern Italy. J Natl Cancer Inst Monogr 82(17):1407–1411
Alizadeh AM, Roshandel G, Roudbarmohammadi S, Roudbary M, Sohanaki H, Ghiasian SA, Taherkhani A, Semnani S, Aghasi M (2012) Fumonisin B1 contamination of cereals and risk of esophageal cancer in a high risk area in Northeastern Iran. Asian Pac J Cancer Prev 13(6):2625–2628
Howard PC, Eppley RM, Stack ME, Warbritton A, Voss KA, Lorentzen RJ, Kovach RM, Bucci TJ (2001) Fumonisin B1 carcinogenicity in a two-year feeding study using F344 rats and B6c3f1 mice. Environ Health Perspect 109:277–282
Gelderblom WCA, Abel S, Smuts CM, Marnewick J, Marasas WFO, Lemmer ER, Ramljak D (2001) Toxicity of cultured material of Fusarium verticilloides strain MRC 826 to nonhuman primates. Environ Health Perspect 109(Supplement 2):291–300
Missmer SA, Suarez L, Felkner M, Wang E, Merrill AH, Rothman KJ, Hendricks KA (2006) Exposure to fumonisins and the occurrence of neural tube defects along the Texas-Mexico border. Environ Health Perspect 114(2):237–241
Marasas WFO, Riley RT, Hendricks KA, Stevens VL, Sadler TW, Gelineau-van WJ, Missmer SA et al (2004) Fumonisins disrupt sphingolipid metabolism, folate transport, and neural tube development in embryo culture and in vivo: a potential risk factor for human neural tube defects among populations consuming fumonisin-contaminated maize. J Nutr 134(4):711–716
Gelineau-van WJ, Voss KA, Stevens VL, Speer MC, Riley RT (2009) Maternal fumonisin exposure as a risk factor for neural tube defects. Adv Food Nutr Res 56:145–181
Marasas WFO, Kellerman TS, Gelderblom WCA, Coetzer JAW, Thiel FG, van der Lugt JJ (1998) Leucoencephalomalacia in a horse induced by fumonisin B1 isolated from Fusarium verticillioides. Onderstepoort J Vet Res 55:197–203
Sheldon JL (1904) A corn mold (Fusarium moniliforme n. sp.). In: Agricultural experiment station of Nebraska: 17th annual report
Kriek NPJ, Kellerman TS, Marasas WFO (1981) A comparative-study of the toxicity of Fusarium verticillioides (=F. moniliforme) to horses, primates, pigs, sheep and rats. Onderstepoort J Vet Res 48(2):129–131
Osweiler GD, Ross PF, Wilson TM, Nelson PE, Witte ST, Carson TL, Rice LG, Nelson HA (1992) Characterization of an epizootic of pulmonary-edema in swine associated with fumonisin in corn screenings. J Vet Diagn Invest 4(1):53–59
Harrison LR, Colvin BM, Greene JT, Newman LE, Cole JR (1990) Pulmonary oedema and hydrothorax in swine produced by fumonisin B1, a toxic metabolite of Fusarium verticillioides. J Vet Diagn Invest 2:217–221
Gumprecht LA, Beasley VR, Weigel RM, Parker HM, Tumbleson ME, Bacon CW, Meredith FI, Haschek WM (1998) Development of fumonisin-induced hepatotoxicity and pulmonary edema in orally dosed swine: morphological and biochemical alterations. Toxicol Pathol 26(6):777–788
Haschek WM, Gumprecht LA, Smith G, Tumbleson ME, Constable PD (2001) Fumonisin toxicosis in swine: an overview of porcine pulmonary edema and current perspectives. Environ Health Perspect 109:251–257
Delgado JE, Wolt JD (2010) Fumonisin B1 and implications in nursery swine productivity: a quantitative exposure assessment. J Anim Sci 88(11):3767–3777
Delgado JE, Wolt JD (2011) Fumonisin B1 toxicity in grower-finisher pigs: a comparative analysis of genetically engineered Bt corn and non-Bt corn by using quantitative dietary exposure assessment modeling. Int J Environ Res Public Health 8(8):3179–3190
Logrieco A, Mule G, Moretti A, Bottalico A (2002) Toxigenic Fusarium species and mycotoxins associated with maize ear rot in Europe. Eur J Plant Pathol 108(7):597–609
Gelineau van Waes J, Maddox J, Ashley-Koch A, Gregory S, Torres de Matute O, Voss KA, Riley RT (2011) Evaluating human exposure to fumonisins in Guatemala and its possible role as a contributing factor to neural tube defects. Phytopathology 101(6):S222
Munkvold GP, Desjardins AE (1997) Fumonisins in maize—can we reduce their occurrence? Plant Dis 81(6):556–565
Egmond HP, Jonker MA (2004) Current regulations governing mycotoxin limits in food. In: Magan N, Olsen M (eds) Mycotoxins in food: detection and control. CRC, Boca Raton
Liu J, Bell AA, Stipanovic R, Puckhaber L, Shim W (2011) A polyketide synthase gene and an aspartate kinase like gene are required for the biosynthesis of fusaric acid in Fusarium oxysporum f. sp. vasinfectum. In: Abstract of the proceedings of the Beltwide Cotton Conferences, Marriott Marquis, Atlanta, 5–7 Jan 2011
Brown DW, Butchko RAE, Busman M, Proctor RH (2012) Identification of gene clusters associated with fusaric acid, fusarin, and perithecial pigment production in Fusarium verticillioides. Fungal Genet Biol 49(7):521–532
Brown DW, Lee SH, Kim LH, Ryu JG, Lee S, Seo Y, Kim YH et al (2015) Identification of a 12-gene fusaric acid biosynthetic gene cluster in Fusarium species through comparative and functional genomics. Mol Plant Microbe Interact 28(3):319–332
Bryden WL, Logrieco A, Abbas HK (2001) Other significant Fusarium mycotoxins. In: Summerell BA, Leslie JF, Backhouse D, Bryden WL, Burgess LW (eds) Fusarium: Paul E. Nelson memorial symposium. APS Press, St. Paul
Scarpino V, Reyneri A, Vanara F, Scopel C, Causin R, Blandino M (2015) Relationship between European corn borer injury, Fusarium proliferatum and F. subglutinans infection and moniliformin contamination in maize. Field Crops Res 183:69–78
Han Z, Tangni EK, Huybrechts B, Munaut F, Scauflaire J, Wu A, Callebaut A (2014) Screening survey of co-production of fusaric acid, fusarin C, and fumonisins B1, B2 and B3 by Fusarium strains grown in maize grains. Mycotoxin Res 30(4):231–240
Niehaus EM, Kleigrewe K, Wiemann P, Studt L, Sieber CMK, Connolly LR, Freitag M et al (2013) Genetic manipulation of the Fusarium fujikuroi fusarin gene cluster yields insight into the complex regulation and fusarin biosynthetic pathway. Chem Biol 20(8):1055–1066
Kleigrewe K, Soehnel AC, Humpf HU (2011) A new high-performance liquid chromatography-tandem mass spectrometry method based on dispersive solid phase extraction for the determination of the mycotoxin fusarin C in corn ears and processed corn samples. J Agric Food Chem 59(19):10470–10476
Bottalico A, Logrieco A, Ritieni A, Moretti A, Randazzo G, Corda P (1995) Beauvericin and fumonisin B1 in preharvest Fusarium moniliforme maize ear rot in Sardinia. Food Addit Contam 12(4):599–607
Moretti A, Logrieco A, Bottalico A, Ritieni A, Fogliano V, Randazzo G (1996) Diversity in beauvericin and fusaproliferin production by different populations of Gibberella fujikuroi (Fusarium section Liseola). Sydowia 48(1):44–56
EFSA CONTAM Panel (EFSA Panel on Contaminants in the Food Chain) (2014) Scientific opinion on the risks to human and animal health related to the presence of beauvericin and enniatins in food and feed. EFSA J 12(8):3802
Ritieni A, Fogliano V, Randazzo G, Scarallo A, Logrieco A, Moretti A, Mannina L, Bottalico A (1995) Isolation and characterization of fusaproliferin, a new toxic metabolite from Fusarium proliferatum. Nat Toxins 3(1):17–20
Munkvold G, Stahr HM, Logrieco A, Moretti A, Ritieni A (1998) Occurrence of fusaproliferin and beauvericin in Fusarium-contaminated livestock feed in Iowa. Appl Environ Microbiol 64(10):3923–3926
Pavlovkin J, Jaskova K, Mistrikova I, Tamas L (2011) Impact of fusaproliferin on primary roots of maize cultivars differing in their susceptibility to Fusarium. Biologia 66(6):1044–10451
Santini A, Meca G, Uhlig S, Ritieni A (2012) Fusaproliferin, beauvericin and enniatins: occurrence in food—a review. World Mycotoxin J 5(1):71–81
Díaz Arias MM, Leandro LF, Munkvold GP (2013) Aggressiveness of Fusarium species and impact of root infection on growth and yield of soybean. Phytopathology 103:822–832
Marin P, Moretti A, Ritieni A, Jurado M, Vazquez C, Gonzalez-Jaen MT (2012) Phylogenetic analyses and toxigenic profiles of Fusarium equiseti and Fusarium acuminatum isolated from cereals from Southern Europe. Food Microbiol 31(2):229–237
Nagy R, Hornok L (1994) Electrophoretic karyotype differences between 2 subspecies of Fusarium acuminatum. Mycologia 86(2):203–208
Nichea MJ, Cendoya E, Zachetti VGL et al (2015) Mycotoxin profile of Fusarium armeniacum isolated from natural grasses intended for cattle feed. World Mycotoxin J 8(4):451–457
Ellis ML, Arias MMD, Leandro LF, Munkvold GP (2012) First report of Fusarium armeniacum causing seed rot and root rot on soybean (Glycine max) in the United States. Plant Dis 96(11):1693
Miedaner T, Caixeta F, Talas F (2013) Head-blighting populations of Fusarium culmorum from Germany, Russia, and Syria analyzed by microsatellite markers show a recombining structure. Eur J Plant Pathol 137(4):743–752
van der Lee T, Zhang H, van Diepeningen A, Waalwijk C (2015) Biogeography of Fusarium graminearum species complex and chemotypes: a review. Food Addit Contam Part A Chem Anal Control Expo Risk Assess 32(4):453–460
Lazreg F, Belabid L, Sanchez J, Gallego E, Garrido-Cardenas JA, Elhaitoum A (2014) First report of Fusarium equiseti causing damping-off disease on aleppo pine in Algeria. Plant Dis 98(9):1268–1269
Garibaldi A, Gilardi G, Ortu G, Gullino ML (2015) First report of leaf spot of wild rocket (Diplotaxis tenuifolia) caused by Fusarium equiseti in Italy. Plant Dis 99(8):1183–1184
Brian PW, Norris GLF, Hemming HG, Dawkins AW, Grove JF, Lowe D (1961) Phytotoxic compounds produced by Fusarium equiseti. J Exp Bot 12(1):1–12
Goldschmied-Reouven A, Friedman J, Block CS (1993) Fusarium spp. isolated from non-ocular sites: a 10 year experience at an Israeli General Hospital. J Mycol Med 3(2):99–102
Nirenberg HL (1976) Untersuchungen uber die morphologische und biologische differenzierung in der Fusarium section Liseola. Mitteilungen aus der biologischen bundesanstalt fur land–und forstwirtschaft (Berlin-Dahlem) 169:1–117
Kuhlman EG (1982) Varieties of Gibberella fujikuroi with Anamorphs in Fusarium section Liseola. Mycologia 74(5):759–768
Leslie JF (1995) Gibberella fujikuroi—available populations and variable traits. Can J Bot 73:S282–S291
Watanabe T, Umehara Y (1977) Perfect state of causal fungus of bakanae disease of rice plants recollected at Toyama. T Mycol Soc Jpn 18(2):136–142
Ploetz RC (2001) Significant diseases in the tropics that are caused by species of Fusarium. In: Summerell BA, Leslie JF, Backhouse D, Bryden WL, Burgess LW (eds) Fusarium: Paul E. Nelson memorial symposium. APS Press, St. Paul
Proctor RH, Plattner RD, Brown DW, Seo JA, Lee YW (2004) Discontinuous distribution of fumonisin biosynthetic genes in the Gibberella fujikuroi species complex. Mycol Res 108:815–822
Snyder WC, Hansen HN, Oswald JW (1957) Cultivars of the fungus, Fusarium. J Madras Univ 27:185–192
O’Donnell K, Ward TJ, Geiser DM, Kistler HC, Aoki T (2004) Genealogical concordance between the mating type locus and seven other nuclear genes supports formal recognition of nine phylogenetically distinct species within the Fusarium graminearum clade. Fungal Genet Biol 41(6):600–623
Starkey DE, Ward TJ, Aoki T, Gale LR, Kistler HC, Geiser DM, Suga H et al (2007) Global molecular surveillance reveals novel Fusarium head blight species and trichothecene toxin diversity. Fungal Genet Biol 44(11):1191–1204
Barros GG, Alaniz Zanon MS, Chiotta ML, Reynoso MM, Scandiani MM, Chulze SN (2014) Pathogenicity of phylogenetic species in the Fusarium graminearum complex on soybean seedlings in Argentina. Eur J Plant Pathol 138(2):215–222
Broders KD, Lipps PE, Paul PA, Dorrance AE (2007) Evaluation of Fusarium graminearum associated with corn and soybean seed and seedling disease in Ohio. Plant Dis 91(9):1155–1160
Bilgi VN, Bradley CA, Mathew FM, Ali S, Rasmussen JB (2011) Root rot of dry edible bean caused by Fusarium graminearum. Plant Health Prog. doi:10.1094/PHP-2011-0425-01-RS
Vesonder RF, Ciegler A, Jensen AH (1973) Isolation of emetic principle from Fusarium-infected corn. Appl Microbiol 26(6):1008–1010
Yoshizawa T, Morooka N (1973) Deoxynivalenol and its monoacetate - new mycotoxins from Fusarium roseum and moldy barley. Agric Biol Chem 37(12):2933–2934
Kelly AC, Clear RM, O'Donnell K, McCormick S, Turkington TK, Tekauz A, Gilbert J et al (2015) Diversity of Fusarium head blight populations and trichothecene toxin types reveals regional differences in pathogen composition and temporal dynamics. Fungal Genet Biol 82:22–31
Ellis ML, Munkvold GP (2014) Trichothecene genotype of Fusarium graminearum isolates from soybean (Glycine max) seedling and root diseases in the United States. Plant Dis 98(7):1012–1013
Barros G, Alaniz Zanon MS, Abod A, Oviedo MS, Ramirez ML, Reynoso MM, Torres A, Chulze S (2012) Natural deoxynivalenol occurrence and genotype and chemotype determination of a field population of the Fusarium graminearum complex associated with soybean in Argentina. Food Addit Contam Part A Chem Anal Control Expo Risk Assess 29(2):293–303
Varga E, Wiesenberger G, Hametner C, Ward TJ, Dong Y, Schoefbeck D, McCormick S et al (2015) New tricks of an old enemy: isolates of Fusarium graminearum produce a type a trichothecene mycotoxin. Environ Microbiol 17(8):2588–2600
Liang JM, Xayamongkhon H, Broz K, Dong Y, McCormick SP, Abramova S, Ward TJ, Ma ZH, Kistler HC (2014) Temporal dynamics and population genetic structure of Fusarium graminearum in the upper midwestern United States. Fungal Genet Biol 73:83–92
Backhouse D (2014) Global distribution of Fusarium graminearum, F. asiaticum and F. boothii from wheat in relation to climate. Eur J Plant Pathol 139(1):161–173
Gale LR, Harrison SA, Ward TJ, O’Donnell K, Milus EA, Gale SW, Kistler HC (2011) Nivalenol-type populations of Fusarium graminearum and F. asiaticum are prevalent on wheat in Southern Louisiana. Phytopathology 101(1):124–134
Kawakami A, Kato N, Sasaya T, Tomioka K, Inoue H, Miyasaka A, Hirayae K (2015) Gibberella ear rot of corn caused by Fusarium asiaticum in Japan. J Gen Plant Pathol 81(4):324–327
Zhu P, Wu L, Liu L, Huang L, Wang Y, Tang W, Xu L (2013) Fusarium asiaticum: an emerging pathogen jeopardizing postharvest asparagus spears. J Phytopathol 161(10):696–703
Lee T, Lee SH, Shin JY, Kim HK, Yun SH, Kim HY, Lee S, Ryu JG (2014) Comparison of trichothecene biosynthetic gene expression between Fusarium graminearum and Fusarium asiaticum. Plant Pathol J 30(1):33–42
Del Ponte EM, Spolti P, Ward TJ, Gomes LB, Nicolli CP, Kuhnem PR, Silva CN, Tessmann DJ (2015) Regional and field-specific factors affect the composition of Fusarium head blight pathogens in subtropical no-till wheat agroecosystem of Brazil. Phytopathology 105(2):246–254
Boutigny AL, Ward TJ, Van Coller GJ, Flett B, Lamprecht SC, O'Donnell K, Viljoen A (2011) Analysis of the Fusarium graminearum species complex from wheat, barley and maize in South Africa provides evidence of species-specific differences in host preference. Fungal Genet Biol 48(9):914–920
Desjardins AE, Proctor RH (2011) Genetic diversity and trichothecene chemotypes of the Fusarium graminearum clade isolated from maize in Nepal and identification of a putative new lineage. Fungal Biol 115(1):38–48
Sampietro DA, Diaz CG, Gonzalez V, Vattuone MA, Ploper LD, Catalan CAN, Ward TJ (2011) Species diversity and toxigenic potential of Fusarium graminearum complex isolates from maize fields in Northwest Argentina. Int J Food Microbiol 145(1):359–364
Toth B, Mesterhazy A, Horvath Z, Bartok T, Varga M, Varga J (2005) Genetic variability of central European isolates of the Fusarium graminearum species complex. Eur J Plant Pathol 113(1):35–45
Umpierrez-Failache M, Garmendia G, Pereyra S, Rodriguez-Haralambides A, Ward TJ, Vero S (2013) Regional differences in species composition and toxigenic potential among Fusarium head blight isolates from Uruguay indicate a risk of nivalenol contamination in new wheat production areas. Int J Food Microbiol 166(1):135–140
Gomes LB, Ward TJ, Badiale-Furlong E, Del Ponte EM (2015) Species composition, toxigenic potential and pathogenicity of Fusarium graminearum species complex isolates from Southern Brazilian rice. Plant Pathol 64(4):980–987
Somma S, Petruzzella AL, Logrieco AF, Meca G, Cacciola OS, Moretti A (2014) Phylogenetic analyses of Fusarium graminearum strains from cereals in Italy, and characterisation of their molecular and chemical chemotypes. Crop Pasture Sci 65(1):52–60
Boutigny AL, Ward TJ, Ballois N, Iancu G, Ioos R (2014) Diversity of the Fusarium graminearum species complex on french cereals. Eur J Plant Pathol 138(1):133–148
Monds RD, Cromey MG, Lauren DR, di Menna M, Marshall J (2005) Fusarium graminearum, F. cortaderiae and F. pseudograminearum in New Zealand: molecular phylogenetic analysis, mycotoxin chemotypes and co-existence of species. Mycol Res 109:410–420
Sampietro DA, Ficoseco MEA, Jimenez CM, Vattuone MA, Catalan CA (2012) Trichothecene genotypes and chemotypes in Fusarium graminearum complex strains isolated from maize fields of Northwest Argentina. Int J Food Microbiol 153:229–233
Spolti P, Barros NC, Gomes LB, dos Santos J, Del Ponte EM (2012) Phenotypic and pathogenic traits of two species of the Fusarium graminearum complex possessing either 15-ADON or NIV genotype. Eur J Plant Pathol 133(3):621–629
Lamprecht SC, Tewoldemedhin YT, Botha WJ, Calitz FJ (2011) Fusarium graminearum species complex associated with maize crowns and roots in the Kwazulu-Natal Province of South Africa. Plant Dis 95(9):1153–1158
Fu M, Li RJ, Guo CC, Pang MH, Liu YC, Dong JG (2015) Natural incidence of Fusarium species and fumonisins B1 and B2 associated with maize kernels from nine provinces in China in 2012. Food Addit Contam Part A Chem Anal Control Expo Risk Assess 32(4):503–511
Nicolli CP, Spolti P, Tibola CS, Fernandes JMC, Del Ponte EM (2015) Fusarium head blight and trichothecene production in wheat by Fusarium graminearum and F. meridionale applied alone or in mixture at post-flowering. Trop Plant Pathol 40(2):134–140
Torp M, Nirenberg HI (2004) Fusarium langsethiae sp. nov. on cereals in Europe. Int J Food Microbiol 95(3):247–256
Torp M, Langseth W (1999) Production of T-2 toxin by a Fusarium resembling Fusarium poae. Mycopathologia 147(2):89–96
Imathiu SM, Ray RV, Back MI, Hare MC, Edwards SG (2013) Fusarium langsethiae—a HT-2 and T-2 toxins producer that needs more attention. J Phytopathol 161:1–10
Infantino A, Santori A, Aureli G, Belocchi A, De Felice S, Tizzani L, Lattanzio VMT, Haidukowski M, Pascale M (2015) Occurrence of Fusarium langsethiae strains isolated from durum wheat in Italy. J Phytopathol 163:612–619
Baayen RP, O’Donnell K, Bonants PJM, Cigelnik E, Kroon LP, Roebroeck EJA, Waalwijk C (2000) Gene genealogies and AFLP analyses in the Fusarium oxysporum complex identify monophyletic and nonmonophyletic formae speciales causing wilt and rot disease. Phytopathology 90(8):891–900
O’Donnell K, Kistler HC, Cigelnik E, Ploetz RC (1998) Multiple evolutionary origins of the fungus causing panama disease of banana: concordant evidence from nuclear and mitochondrial gene genealogies. Proc Natl Acad Sci U S A 95(5):2044–2049
Skovgaard K, Rosendahl S, O’Donnell K, Nirenberg HI (2003) Fusarium commune is a new species identified by morphological and molecular phylogenetic data. Mycologia 95(4):630–636
Laurence MH, Summerell BA, Burgess LW, Liew ECY (2014) Genealogical concordance phylogenetic species recognition in the Fusarium oxysporum species complex. Fungal Biol 118(4):374–384
Vanheule A, Audenaert K, Höfte M, Warris S, van de Geest H, Waalwijk C, Haesaert G, van der Lee T (2015) Presenting the fully assembled genome of Fusarium poae: repeats shed light on a cryptic sexual cycle. 13th European Fusarium Seminar Martina Franca, Italy, 10–14 May 2015, 39
Amatulli MT, Spadaro D, Gullino ML, Garibaldi A (2012) Conventional and real-time PCR for the identification of Fusarium fujikuroi and Fusarium proliferatum from diseased rice tissues and seeds. Eur J Plant Pathol 134(2):401–408
Chulze SN, Ramirez ML, Farnochi MC, Pascale M, Visconti A, March G (1996) Fusarium and fumonisin occurrence in Argentinian cool at different ear maturity stages. J Agric Food Chem 44(9):2797–2801
Nirenberg HI (1995) Morphological differentiation of Fusarium sambucinum Fuckel sensu stricto, F. torulosum (Berk and Curt) Nirenberg comb. nov. and F. venenatum Nirenberg sp. nov. Mycopathologia 129(3):131–141
Chehri K, Salleh B, Zakaria L (2015) Morphological and phylogenetic analysis of Fusarium solani species complex in Malaysia. Microb Ecol 69(3):457–471
O’Donnell K, Sutton DA, Fothergill A et al (2008) Molecular phylogenetic diversity, multilocus haplotype nomenclature, and in vitro antifungal resistance within the Fusarium solani species complex. J Clin Microbiol 46:2477–2490
Short DPG, O’Donnell K, Thrane U, Nielsen KF, Zhang N, Juba JH, Geiser DM (2013) Phylogenetic relationships among members of the Fusarium solani species complex in human infections and the descriptions of F. keratoplasticum sp. nov. and F. petroliphilum stat. nov. Fungal Genet Biol 53:59–70
Lenc L, Lukanowski A, Sadowski C (2008) The use of PCR amplification in determining the toxigenic potential of Fusarium sambucinum and F. solani isolated from potato tubers with symptoms of dry rot. Phytopathol Pol 48:13–23
Lenc L (2011) Pathogenicity and potential capacity for producing mycotoxins by Fusarium sambucinum and Fusarium solani isolates derived from potato tubers. Plant Breed Seed Sci 64:23–34
Fumero M, Reynoso M, Chulze S (2015) Fusarium temperatum and Fusarium subglutinans isolated from maize in Argentina. Int J Food Microbiol 199:86–92
Shin JH, Han JH, Lee JK, Kim KS (2014) Characterization of the maize stalk rot pathogens Fusarium subglutinans and F. temperatum and the effect of fungicides on their mycelial growth and colony formation. Plant Pathol J 30(4):397–406
Bottalico A (1998) Fusarium diseases of cereals: species complex and related mycotoxin profiles, in Europe. J Plant Pathol 80(2):85–103
Munkvold GP, Logrieco A, Moretti A, Ferracane R, Ritieni A (2009) Dominance of group 2 and fusaproliferin production by Fusarium subglutinans from Iowa maize. Food Addit Contam Part A Chem Anal Control Expo Risk Assess 26(3):388–394
Scauflaire J, Gourgue M, Callebaut A, Munaut F (2011) Fusarium temperatum sp. nov. from maize: an emergent species closely related to Fusarium subglutinans. Mycologia 103(3):586–597
Desjardins AE, Plattner RD, Gordon TR (2000) Gibberella fujikuroi mating population a and Fusarium subglutinans from teosinte species and maize from Mexico and Central America. Mycol Res 104:865–872
Steenkamp ET, Wingfield BD, Desjardins AE, Marasas WFO, Wingfield MJ (2002) Cryptic speciation in Fusarium subglutinans. Mycologia 94(6):1032–1043
Czembor E, Stepien L, Waskiewicz A (2014) Fusarium temperatum as a new species causing ear rot on maize in Poland. Plant Dis 98(7):1001
Varela CP, Aguin CO, Chaves PM, Ferreiroa MV, Sainz Oses MJ, Scauflaire J, Munaut F, Bande Castro MJ, Mansilla Vazquez JP (2013) First report of Fusarium temperatum causing seedling blight and stalk rot on maize in Spain. Plant Dis 97(9):1252–1253
Lanza F, Mayfield D, Munkvold GP (2016) First report of Fusarium temperatum causing maize seedling blight and seed rot in North America. Plant Dis 100:1019
Zhang H, Luo W, Pan Y, Xu J, Xu JS, Chen WQ, Feng J (2014) First report of Fusarium temperatum causing Fusarium ear rot on maize in Northern China. Plant Dis 98(9):1273
Castanares E, Stenglein SA, Dinolfo MI, Moreno MV (2011) Fusarium tricinctum associated with head blight on wheat in Argentina. Plant Dis 95(4):496
Bottalico A, Perrone G (2002) Toxigenic Fusarium species and mycotoxins associated with head blight in small-grain cereals in Europe. Eur J Plant Pathol 108(7):611–624
Chitrampalam P, Nelson BD Jr (2014) Effect of Fusarium tricinctum on growth of soybean and a molecular-based method of identification. Plant Health Prog. doi:10.1094/PHP-RS-14-0014
Zaher AM, Makboul MA, Moharram AM, Tekwani BL, Calderon AI (2015) A new enniatin antibiotic from the endophyte Fusarium tricinctum Corda. J Antibiot 68(3):197–200
Cuomo V, Randazzo A, Meca G, Moretti A, Cascone A, Eriksson O, Novellino E, Ritieni A (2013) Production of enniatins A, A1, B, B1, B4, J1 by Fusarium tricinctum in solid corn culture: structural analysis and effects on mitochondrial respiration. Food Chem 140(4):784–793
Saccardo PA (1886) Sylloge fungorum omnium hucusque cognitorum, 4th edn. Edwards Bros, Ann Arbor
Wineland GO (1924) An ascigerous stage and synonomy for Fusarium moniliforme. J Agric Res 28:909–922
Moretti A, Mule G, Susca A, Gonzalez-Jaen MT, Logrieco A (2004) Toxin profile, fertility and AFLP analysis of Fusarium verticillioides from banana fruits. Eur J Plant Pathol 110:601–609
Van Hove F, Waalwijk C, Logrieco A, Munaut F, Moretti A (2011) Gibberella musae (Fusarium musae) sp nov., a recently discovered species from banana is sister to F. verticillioides. Mycologia 103(3):570–585
Proctor RH, Brown DW, Plattner RD, Desjardins AE (2003) Co-expression of 15 contiguous genes delineates a fumonisin biosynthetic gene cluster in Gibberella moniliformis. Fungal Genet Biol 38(2):237–249
Zeller KA, Summerell BA, Bullock S, Leslie JF (2003) Gibberella konza (Fusarium konzum) sp nov from prairie grasses, a new species in the Gibberella fujikuroi species complex. Mycologia 95(5):943–954
Leslie JF, Zeller KA, Logrieco A, Mule G, Moretti A, Ritieni A (2004) Species diversity of and toxin production by Gibberella fujikuroi species complex strains isolated from native prairie grasses in Kansas. Appl Environ Microbiol 70(4):2254–2262
Triest D, Stubbe D, De Cremer K, Pierard D, Detandt M, Hendrickx M (2015) Banana infecting fungus, Fusarium musae, is also an opportunistic human pathogen: are bananas potential carriers and source of fusariosis? Mycologia 107(1):46–53
Acknowledgements
The author is grateful to Dr. Robert Proctor, USDA-ARS, Peoria, IL, for contributing information regarding Fusarium genome sequences, and to Ms. Lauren Washington, Iowa State University, for assistance in preparing the manuscript.
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Munkvold, G.P. (2017). Fusarium Species and Their Associated Mycotoxins. In: Moretti, A., Susca, A. (eds) Mycotoxigenic Fungi. Methods in Molecular Biology, vol 1542. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-6707-0_4
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