Host extract modulates metabolism and fumonisin biosynthesis by the plant-pathogenic fungus Fusarium proliferatum

被引:29
|
作者
Stepien, Lukasz [1 ]
Waskiewicz, Agnieszka [2 ]
Wilman, Karolina [1 ]
机构
[1] Polish Acad Sci, Inst Plant Genet, Dept Pathogen Genet & Plant Resistance, PL-60479 Poznan, Poland
[2] Poznan Univ Life Sci, Dept Chem, PL-60625 Poznan, Poland
关键词
FUM1; Fungal biomass measurement; Genetic diversity; Mycotoxin biosynthesis; Plant extract application; FUM1; GENE-EXPRESSION; VERTICILLIOIDES; CLUSTER; GROWTH; DIVERSITY; LIGHT;
D O I
10.1016/j.ijfoodmicro.2014.10.020
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Fusarium proliferatum is a common pathogen able to infect a broad range of agriculturally important crops. Recently, some evidence for genetic variance among the species genotypes in relation to their plant origin has been reported. Mycotoxin contamination of plant tissues is the most important threat caused by F. proliferatum and fumonisins B (FBs) are the principal mycotoxins synthesized. The toxigenic potential of the pathogen genotypes is variable and also the reaction of different host plant species on the infection by pathogen is different. The objective of present study was to evaluate the impact of the extracts on the growth and fumonisin biosynthesis by 32 F. proliferatum strains originating from different host species (A-asparagus, M-maize, G-garlic, PS-pea and P-pineapple), and how it changes the secondary metabolism measured by fumonisin biosynthesis. The average strain dry weight was 65.2 mg for control conditions and it reached 180.7 mg, 100.5 mg, 76.6 mg, 126.2 mg and 51.1 mg when pineapple, asparagus, maize, garlic and pea extracts were added, respectively. In the second experiment the extracts were added after 5 days of culturing of the representative group of strains, displaying diverse reaction to the extract presence. Also, the influence of stationary vs. shaken culture was examined. Mean biomass amounts for shaken cultures of 15 chosen strains were as follows: 37.4 mg of dry weight for control culture (C), 219.6 mg (P), 113 mg (A), 93.6 mg (M), 62 mg (G) and 48 mg (PS), respectively. For stationary cultures, the means were as follows: C-57.4 mg, P-355.6 mg, A-291.6 mg, M-191.1 mg, G-171.1 mg and PS-58.9 mg. Few strains showed differential growth when stationary/shaken culture conditions were applied. Almost all strains synthesized moderate amounts of fumonisins in control conditions less than 10 ng/mu L, regardless of the origin and host species. Few strains were able to produce over 100 ng/mu L, of FBs when pineapple extract was added, twelve strains synthesized more than 10 ng/mu L under asparagus extract induction and the pea extract was the most efficient inhibitor of fumonisin biosynthesis. The general impact of the extracts on the fungal biomass amounts was similar, regardless of the host plant origin of the fungal genotypes studied. The evaluation of FBs content has shown differential reaction of some strains, which may contribute to their aggressiveness and pathogenicity. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:74 / 81
页数:8
相关论文
共 50 条
  • [31] Host extracts induce changes in the proteome of plant pathogen Fusarium proliferatum
    Gorna, Karolina
    Perlikowski, Dawid
    Kosmala, Arkadiusz
    Stepien, Lukasz
    FUNGAL BIOLOGY, 2017, 121 (08) : 676 - 688
  • [32] Migratory moths as dispersal vectors of an introduced plant-pathogenic fungus in Japan
    Shinji Sugiura
    Kazuo Yamazaki
    Biological Invasions, 2007, 9 : 101 - 106
  • [33] Draft Genome Sequence of Dactylonectria macrodidyma, a Plant-Pathogenic Fungus in the Nectriaceae
    Malapi-Wight, Martha
    Salgado-Salazar, Catalina
    Demers, Jill
    Veltri, Daniel
    Crouch, Jo Anne
    GENOME ANNOUNCEMENTS, 2015, 3 (02)
  • [34] Horizontal Chromosome Transfer, a Mechanism for the Evolution and Differentiation of a Plant-Pathogenic Fungus
    Akagi, Yasunori
    Akamatsu, Hajime
    Otani, Hiroshi
    Kodama, Motoichiro
    EUKARYOTIC CELL, 2009, 8 (11) : 1732 - 1738
  • [35] A DOUBLE-STRANDED-RNA MYCOVIRUS FROM THE PLANT-PATHOGENIC FUNGUS, FUSARIUM-SOLANI F SP ROBINIAE
    NOGAWA, M
    SHIMOSAKA, M
    KAGEYAMA, T
    OKAZAKI, M
    FEMS MICROBIOLOGY LETTERS, 1993, 110 (02) : 153 - 158
  • [36] A slicing mechanism facilitates host entry by plant-pathogenic Phytophthora
    Bronkhorst, Jochem
    Kasteel, Michiel
    van Veen, Stijn
    Clough, Jess M.
    Kots, Kiki
    Buijs, Jesse
    van der Gucht, Jasper
    Ketelaar, Tijs
    Govers, Francine
    Sprakel, Joris
    NATURE MICROBIOLOGY, 2021, 6 (08) : 1000 - +
  • [37] A novel mycovirus isolated from the plant-pathogenic fungus Botryosphaeria dothidea
    Liu, Hong
    Wang, Hui
    Zhou, Qian
    ARCHIVES OF VIROLOGY, 2021, 166 (04) : 1267 - 1272
  • [38] Sulfur metabolism-mediated fungal glutathione biosynthesis is essential for oxidative stress resistance and pathogenicity in the plant pathogenic fungus Fusarium graminearum
    Park, Jiyeun
    Han, Jae Woo
    Lee, Nahyun
    Kim, Sieun
    Choi, Soyoung
    Lee, Hyun-Hee
    Kim, Jung-Eun
    Seo, Young-Su
    Choi, Gyung Ja
    Lee, Yin-Won
    Kim, Hun
    Son, Hokyoung
    MBIO, 2024, 15 (01):
  • [39] Migratory moths as dispersal vectors of an introduced plant-pathogenic fungus in Japan
    Sugiura, Shinji
    Yamazaki, Kazuo
    BIOLOGICAL INVASIONS, 2007, 9 (02) : 101 - 106
  • [40] Virulence genes and the evolution of host specificity in plant-pathogenic fungi
    van der Does, H. Charlotte
    Rep, Martijn
    MOLECULAR PLANT-MICROBE INTERACTIONS, 2007, 20 (10) : 1175 - 1182