Clavicipitaceous endophytes: Their ability to enhance resistance of grasses to multiple stresses

By G. Kuldau, C. Bacon. 2008

337 citations recorded by the source corpus.

Subfields: Ecology, Evolution, Behavior and Systematics, Molecular Biology

View Paper: https://www.semanticscholar.org/paper/835792ab0a07270ddc30069692ed2ebfd1991fc5

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Ecology, Evolution, Behavior and Systematics

1. L. Jaber
2. D. M. Hinton
3. C. Bacon
4. B. Ownley
5. F. Lin
6. M. Márquez
7. Chu-long Zhang
8. L. D. Acuña

In Molecular Biology

1. L. Jaber
2. B. Ownley
3. C. Douanla-Meli
4. C. Bacon
5. E. Langer
6. F. T. Mouafo
7. G. Bills
8. I. Zabalgogeazcoa

Citations in the corpus

• Fungal endophyte diversity and community patterns in healthy and yellowing leaves of Citrus limon (2013, background): “It is also recognized that these interactions are mediated by means of fungal metabolites (Kuldau & Bacon 2008) that are, however, also active against other fungi (Christensen 1996; Campanile et al. 2007; Zhang et al. 2009; Sumarah et al. 2011).”
• Fungal endophyte negative effects on herbivory are enhanced on intact plants and maintained in a subsequent generation (2010, background): “…& Fagan, 2002); mainly by the production of secondary compounds, including alkaloids, which benefit © 2010 The Authors Journal compilation © 2010 The Royal Entomological Society 25 plants by increasing their competitive ability and resistance to biotic and abiotic stresses (Kuldau & Bacon, 2008).”
• FUSARIUM VERTICILLIOIDES: MANAGING THE ENDOPHYTIC ASSOCIATION WITH MAIZE FOR REDUCED FUMONISINS ACCUMULATION (2008, background): “…from the apoplasm of the intercellular spaces, which have adequate nutrients for both primary and secondary metabolism (Kursanov and Brovchenko, 1970; Epel and Banduski, 1990; Hartung et al., 1992; Canny, 1995; Whittaker and Botha, 1997; Asis, 2003; Tejera et al., 2006; Kuldau and Bacon, 2008).”
• Can we use entomopathogenic fungi as endophytes for dual biological control of insect pests and plant pathogens (2018, background): “These clavicipitaceous endophytes are generally known to confer an array of potential fitness benefits to their grass host plants (Kuldau and Bacon, 2008).”
• Endophyte-mediated adjustments in host morphology and physiology and effects on host fitness traits in grasses (2012, background): “However, it is beginning to emerge (see Tanaka et al. 2006; Schardl et al. 2007; Kuldau & Bacon 2008; Rodriguez et al. 2008; Rasmussen et al. 2009; Faeth et al. 2010; Rudgers et al. 2010; Torres & White 2010) that endophytes are not passive inhabitants of plants, but rather are active colonizers of…”
• Endophytic fungi as biocontrol agents: elucidating mechanisms in disease suppression (2018, background): “Growth promotion through nutrient acquisition (nitrogen, phosphorous and essential minerals) ormodulating plant hormone levels can also improve general plant health and thus protection against diseases (Kuldau and Bacon 2008; Franken 2012; Berthelot et al. 2016).”
• Role of Diverse Non-Systemic Fungal Endophytes in Plant Performance and Response to Stress: Progress and Approaches (2010, background): “Although mycorrhizal fungi and grass clavicipitaceous endophyte-mediated stress resistance has been well documented (Pozo and Azcon-Aguilar 2007; Kuldau and Bacon 2008), few details are known about the ecological significance of type II endophytes.”
• Endophytic mycobiota of leaves and roots of the grass Holcus lanatus (2010, background): “Several species of these genera have characteristics which convert them in “model endophytes”: symptomless systemic colonization of the aerial tissues of the host plant, efficient vertical transmission by seed, and a mutualistic interaction with their hosts, which show increased tolerance to several”