Koon-Hui
Wang
University of Florida, Department of
Entomology and Nematology, P.O. Box 110620, Gainesville, FL 32611-0620, U.S.A.
(Last updated January, 2002)
There are various
ways for soil-borne fungi to suppress nematode multiplication. A detailed
review of fungi as biocontrol agents against plant-parasitic nematodes has been
published (Kerry and Jaffee, 1997). In summary, there are four mechanisms that fungi
use to suppress nematodes. Some of these interactions are direct whereas others
are indirect. The direct mechanism is performed by 1) fungi that feed on
nematodes directly, known as nematophagous fungi; fungi interact with nematodes
in an indirect manner by several mechanisms including: 2) fungi that kill nematodes
by mycotoxin (Barron and Thorne,
1987) or 3) through the destruction of the feeding sites
of sedentary nematodes in roots (Glawe
and Stiles, 1989); 4) fungi that are nonpathogenic to plants, but
compete with nematodes in roots and significantly reduce nematode
multiplication (Sikora, 1992). Many of these fungi are used as potential nematode
biocontrol agents; 5) Mycorrhizal fungi improve the growth of nematode infected
plants and may also affect nematode development (Hussey and Roncadori, 1982).
This article
summarizes groups of nematophagous fungi according to their feeding habits:
A) Nematode-trapping fungi
Facultative fungi that form trapping structure to trap nematodes. There are 6 types of traps reported by Barron (1977).
adhesive hyphae:
eg. Zygomycotina
Stylopage
Cystopage
adhesive traps:
eg. Deuteromycota
Monacrosporium
cionopagum (branches)
M.
ellipsosporum (knobs)
Arthrobotrys
oligospora (networks)
non-adhesive traps
eg. Deuteromycota
Arthrobotrys
dactyloides (constricting ring)
(non-constricting
ring)
B) Facultative parasitic fungi attacking
sedentary stages of nematodes (Kerry and Jaffee, 1997)
These
are facultative fungi that are commonly soil saprophytes, and are opportunistic
fungi isolated from the sedentary stages (female and egg stages) of sedentary
nematodes such as Heterodera, Globodera, and Meloidogyne. They do
not form specialized infection structures except appressoria. They can survive
and proliferate in soil in the absence of nematodes.
eg.
Hyphomycotina
Acremonium
Cylindrocarpon
Fusarium
Paecilomyces
Verticillium
C) Endoparasitic fungi (Kerry and Jaffee,
1997)
These are obligate parasitic fungi that have limited growth in soil outside the colonized nematode cadaver.
They can infect vermiform nematodes by
producing adhesive spores attached to cuticle of passing nematodes.
eg. Hyphomycotina
Hirsutella
rhossiliensis
Drechmeria coniospora
Verticillium spp.
Some can infect vermiform nematodes by
producing conidia spores that can be ingested by nematodes.
Harposporium
anguillulae
Some can infect vermiform nematodes by
producing motile zoospores that encyst on the nematode’s surface.
eg. Oomycota
Myzocytium spp.
Lagenidium spp.
Chytridiomycota
Catenaria anguillulae
Some can infect sedentary nematodes when the
nematodes were exposed on the root surface.
eg. Oomycota
Nematophora gynophila
Further
information on nematode biocontrol by nematode-antagonistic fungi can be
obtained through:
http://sacs.cpes.peachnet.edu/nemabc/
http://www.area.ba.cnr.it/~e085ac01/bkfair3444.html
http://www.ag.auburn.edu/bci/nematolo.htm
Table 1. Effect of soil edaphic factors on distribution of nematode-antagonistic fungi (Gray, 1985).
|
Nematophagous fungi |
Organic matter |
pH |
Moisture |
Nematode densities |
|
Nematode-trapping |
NSz |
low |
NS |
NS |
|
net |
lowy |
low |
low |
NS |
|
ring |
highx |
low |
high |
NS |
|
adhesive hyphae |
NS |
high |
NS |
NS |
|
adhesive branch |
NS |
NS |
NS |
high |
|
adhesive knobs |
NS |
low |
NS |
NS |
|
Endoparasites |
high |
low |
high |
high |
zNS =effects of the
edaphic factors is not significant.
ylow=lower value of the edaphic
factor is preferred by the group of nematophagous fungi.
xhigh=higher value of the
edaphic factor is preferred by the group of nematophagous fungi.
There are two
groups of nematode-trapping fungi (NTF): saprophytic and parasitic NTF (Cooke, 1963).
v
Saprophytic
NTF—form 3-dimensional-network traps in response to the presence of nematodes.
Under low nematode population densities, they remain saprophytic. Therefore,
they are regarded as inefficient nematode-trappers.
v Parasitic NTF—have low saprophytic ability, but form traps spontaneously. This group consists of NTF that form constricting rings, adhesive branches and are more effective nematode trappers than the saprophytic NTF (Jasson, 1982).
Barron, G. L. 1977. The nematode-destroying fungi, Canadian
Biological Publication Ltd.
Barron, G. L., and R. G. Thorne. 1987.
Destruction of nematodes species of Pleurotus.
Canadian Journal of Botany 65: 774-778.
Cooke, R. C. 1963. Ecological
characteristics of nematode-trapping fungi Hyphomycetes. Annual Review of
Applied Biology 52: 431-437.
Glawe, D. A., and C. M. Stiles. 1989.
Colonization of soybean roots by fungi isolated from cysts of Heterodera glycines. Mycologia 81:
797-799.
Gray, N. F. 1985. Ecology of nematophagous
fungi:distribution and habitat. Annual Review of Applied Biology 102: 501-509.
Hussey, R. S., and R. W. Roncadori. 1982.
Vesicular-arbuscular mycorrhizae may limit nematode activity and improve plant
growth. Plant Disease 66: 9-14.
Jasson, H. B. 1982. Predacity by
nematophagous fungi and its relation to the attraction of nematodes. Microbial
Ecology 8: 233-240.
Kerry, B. R., and B. A. Jaffee. 1997. Fungi
as biological control agents for plant parasitic nematodes. in The Mycota K. Esser and P. A. Lemke,
eds., Vol. IV, pp. 204-218. Springer, Verlag Berlin Heidelberg.
Sikora, R. A. 1992. Management of the
antagonistic potential in agricultural ecosystems for the biological control of
plant parasitic nematodes. Annual Review of Phytopathology 30: 245-247.