Superoxide anion and hydrogen peroxide in the yeast antagonist-fruit interaction: A new role for reactive oxygen species in postharvest biocontrol?

被引:109
作者
Macarisin, Dumitru [2 ]
Droby, Samir [1 ]
Bauchan, Gary [3 ]
Wisniewski, Michael [2 ]
机构
[1] Agr Res Org, Volcani Ctr, IL-50250 Bet Dagan, Israel
[2] USDA ARS, Kearneysville, WV 25430 USA
[3] USDA ARS, Elect &Confocal Microscopy Unit, Beltsville, MD 20705 USA
关键词
Postharvest biological control; Yeast antagonists; Reactive oxygen species; Superoxide anion; Hydrogen peroxide; APOPLASTIC OXIDATIVE BURST; ENHANCING DISEASE RESISTANCE; DEFENSE RESPONSES; SUSPENSION CELLS; PLANT DEFENSE; PEACH FRUIT; MECHANISMS; INFECTION; ACID; SUPPRESSION;
D O I
10.1016/j.postharvbio.2010.07.008
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
The importance of reactive oxygen species (ROS) in plant defense responses against certain pathogens is well documented. There is some evidence that microbial biocontrol agents also induce a transient production of ROS in a host plant which triggers local and systemic defense responses to pathogens. The ability of biocontrol agents used to control postharvest diseases to induce defense-related oxidative responses in fruits, however, has not been explored. Here we show that the yeast antagonists, Metschnikowia fructicola (strain 277) and Candida oleophila (strain 182) generate greater levels of super oxide anion (O-2(-)) on intact fruit surfaces (poor in nutrients) then those applied on a nutrient-poor agar medium. Even though yeast antagonists show a high level of O-2(-) on nutrient-rich media, when applied on fruits around wounds (areas abundant in nutrients) accumulation of O-2(-), as detected by nitro blue tetrazolium staining, occurred much more rapidly on the latter. Using laser scanning confocal microscopy we observed that the application of M. fructicola and C. oleophila into citrus and apple fruit wounds correlated with an increase in H2O2 accumulation in host tissue. In citrus fruit, the level of H2O2 around inoculated wounds increased by 4-fold compared to controls (wounds inoculated with water) as early as 18 h after inoculation. Yeast continued to stimulate H2O2 production in citrus fruit up to 66 h after inoculation and H2O2 levels were still 3-fold above the control. Living yeast cells were detected in fruit wounds at this time point indicating the ability of M. fructicola to tolerate host ROS, which has been reported to be an intrinsic characteristic of efficient yeast antagonists. Similar increase in H2O2 accumulation around yeast-inoculated wounds was observed in apple fruit exocarp. The present data, together with our earlier discovery of the importance of H2O2 production in the defense response of citrus flavedo to postharvest pathogens, indicate that the yeast-induced oxidative response in fruit exocarp may be associated with the ability of specific yeast species to serve as biocontrol agents for the management of postharvest diseases. Published by Elsevier B.V.
引用
收藏
页码:194 / 202
页数:9
相关论文
共 38 条
  • [1] Suppression of anti-Candida activity of macrophages by a quorum-sensing molecule, farnesol, through induction of oxidative stress
    Abe, Shigeru
    Tsunashima, Rumi
    Iijima, Ryosuke
    Yamada, Tsuyoshi
    Maruyama, Naho
    Hisajima, Tatsuya
    Abe, Yoshie
    Oshima, Haruyuki
    Yamazaki, Masatoshi
    [J]. MICROBIOLOGY AND IMMUNOLOGY, 2009, 53 (06) : 323 - 330
  • [2] Hydrogen peroxide yields during the incompatible interaction of tobacco suspension cells inoculated with Phytophthora nicotianae
    Able, AJ
    Guest, DI
    Sutherland, MW
    [J]. PLANT PHYSIOLOGY, 2000, 124 (02) : 899 - 910
  • [3] Capsidiol production in pepper fruits (Capsicum annuum L.) induced by arachidonic acid is dependent of an oxidative burst
    Araceli, Arreola-Cortes
    Elda, Castro-Mercado
    Edmundo, Lozoya-Gloria
    Ernesto, Garcia-Pineda
    [J]. PHYSIOLOGICAL AND MOLECULAR PLANT PATHOLOGY, 2007, 70 (1-3) : 69 - 76
  • [4] ACTIVE OXYGEN IN PLANT PATHOGENESIS
    BAKER, CJ
    ORLANDI, EW
    [J]. ANNUAL REVIEW OF PHYTOPATHOLOGY, 1995, 33 : 299 - 321
  • [5] Peroxidase-dependent apoplastic oxidative burst in Arabidopsis required for pathogen resistance
    Bindschedler, Laurence V.
    Dewdney, Julia
    Blee, Kris A.
    Stone, Julie M.
    Asai, Tsuneaki
    Plotnikov, Julia
    Denoux, Carine
    Hayes, Tezni
    Gerrish, Chris
    Davies, Dewi R.
    Ausubel, Frederick M.
    Bolwell, G. Paul
    [J]. PLANT JOURNAL, 2006, 47 (06) : 851 - 863
  • [6] Superoxide signalling required for multicellular development of Dictyostelium
    Bloomfield, G
    Pears, C
    [J]. JOURNAL OF CELL SCIENCE, 2003, 116 (16) : 3387 - 3397
  • [7] Bolwell GP, 1999, FREE RADICAL RES, V31, pS137
  • [8] The apoplastic oxidative burst in response to biotic stress in plants: a three-component system
    Bolwell, GP
    Bindschedler, LV
    Blee, KA
    Butt, VS
    Davies, DR
    Gardner, SL
    Gerrish, C
    Minibayeva, F
    [J]. JOURNAL OF EXPERIMENTAL BOTANY, 2002, 53 (372) : 1367 - 1376
  • [9] Mechanisms for the generation of reactive oxygen species in plant defence - a broad perspective
    Bolwell, GP
    Wojtaszek, P
    [J]. PHYSIOLOGICAL AND MOLECULAR PLANT PATHOLOGY, 1997, 51 (06) : 347 - 366
  • [10] Brown SH, 2008, MOL PLANT PATHOL, V9, P171, DOI [10.1111/j.1364-3703.2007.00454.x, 10.1111/J.1364-3703.2007.00454.X]