14.10 Necrotrophic and biotrophic pathogens of plants
Plant pathogens are often divided into biotrophs and necrotrophs, (and, more recently, hemibiotrophs) according to their lifestyles. The definitions of these terms are:
- biotrophs derive energy from living cells, they are found on or in living plants, can have very complex nutrient requirements and do not kill host plants rapidly;
- necrotrophs derive energy from killed cells; they invade and kill plant tissue rapidly and then live saprotrophically on the dead remains;
- hemibiotrophs have an initial period of biotrophy followed by necrotrophy.
This classification suggests a range of generalisations (Table 1) that together indicate clearly that the biotroph/necrotroph division is biologically meaningful. In particular, the genetic analysis of disease resistance with plants for which the full genomes are available, such as Arabidopsis thaliana, demonstrates that the division is based on how defence against fungal pathogens is controlled. Hane et al. (2020) suggest that this traditional classification (into biotrophs, hemibiotrophs, or necrotrophs) should be replaced by a seven-class scheme of trophic phenotypes based on genome-derived analysis of carbohydrate-active enzyme gene content. It is too early to know how widely this scheme will be applied.
Table 1. Comparison of generalised characteristics of biotrophic and necrotrophic plant pathogens | |
Necrotrophs |
Biotrophs |
Opportunistic, unspecialised (‘non-obligate’) pathogens | Specialised (‘obligate’) pathogens |
Host cells killed rapidly | Cause little damage to the host plant; host cells not killed rapidly, but can induce hypersensitive cell death in incompatible interactions |
Entry unspecialised via wounds or natural openings | Entry specialised e.g. direct (mechanical) entry (powdery mildews) or through natural openings (rusts) |
Secrete copious cell-wall-degrading (lytic) enzymes and toxins | Few if any lytic enzymes or toxins are produced |
Appressoria/haustoria not normally produced | Possess appressoria or haustoria |
Seldom systemic | Often systemic |
Usually attack weak, young or damaged plants | Plants of all ages and vigour attacked |
Wide host range | Narrow host range |
Easy to culture axenically | Not easily cultured axenically |
Survive as competitive saprotrophs | Frequently survive on host or as dormant propagules |
Controlled by quantitative resistance genes (example is Septoria nodorum blotch caused by Stagonospora nodorum) | Controlled by specific (gene-for-gene) resistance genes (for example, tomato leaf mould, the rusts, powdery and downy mildews) |
Growth within host is intercellular and intracellular through dead cells | Growth within host is intercellular |
Controlled by jasmonate- and ethylene-dependent host-defence pathways | Controlled by salicylate-dependent host-defence pathways |
Defence against biotrophic pathogens is largely due to programmed cell death in the host, and to associated activation of defence responses regulated by the salicylic acid-dependent pathway. Necrotrophic pathogens benefit from death of host cells, so they are not limited by this defence, but by responses activated by jasmonate acid and ethylene signalling pathways (see below). Such a ‘mode-of-defence’ division successfully distinguishes necrotrophs and biotrophs but it does limit the biotroph category to fungi that produce haustoria (Oliver & Ipcho, 2004; Glazebrook, 2005).
Table 2 gives some examples of necrotrophic and biotrophic pathogens, and includes some hemibiotrophic pathogens, like Phytophthora infestans, that exhibit characteristics of both biotrophs and necrotrophs.
Table 2. Some common plant pathogens | |||
Necrotrophs |
Biotrophs |
||
Pathogen |
Disease |
Pathogen |
Disease |
Botrytis cinerea | Grey mould |
Blumeria (Erysiphe) graminis | Powdery mildew |
Cochliobolus heterostrophus | Corn leaf blight |
Uromyces fabae | Rust |
Pythium ultimum | Damping off in seedlings |
Ustilago maydis | Maize smut |
Ophiostoma novo-ulmi | Dutch elm disease |
Cladosporium fulvum | Tomato leaf mould |
Fusarium oxysporum | Vascular wilt |
Puccinia graminis | Black stem rust of cereals |
Sclerotinia sclerotiorum | Soft rot |
Phytophthora infestans | Potato late blight |
Hemibiotrophs |
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Cladosporium fulvum, causing
tomato leaf mould (also called a biotroph). Colletotrichum lindemuthianum, causing anthracnose. Magnaporthe grisea, causing rice blast (also called a necrotroph). Phytophthora infestans, causing potato late blight (also called a biotroph by some, necrotroph by others). Mycosphaerella graminicola, causing Septoria leaf blight. |
Updated January, 2020