R. D. Stipanovic, M. H. Wheeler, Jinggao Liu, Alois A. Bell, and Lorraine Puckhaber. USDA-ARS-SPARC, 2765 F&B Road (Bldg 11), Cotton Pathology Research Unit, College Station, TX 77845
Fusarium wilt of cotton is caused by Fusarium oxysporum Sclecht
f. sp. vasinfectum (Atk.) Sny. and Hans (F.o.v.). F.o.v. occurs in most countries where
cotton is grown. Losses in cotton yield
can be especially devastating on farms where soil conditions, nematode
populations, and indigenous populations of the pathogen favor the disease.
A genetically
unique strain of F.o.v. was first
recognized in wilted and dead Upland cotton seedlings in Australia in 1993. Since that time, the pathogen has spread rapidly
despite strict containment practices. On
some Australian farms where it was first discovered, losses above 90% have
forced cotton production to be abandoned.
The Australian strain was inadvertently introduced into the U.S. in at least two shiploads of cottonseed
imported into California
for cattle feed in 2001 and 2002. We
have calculated that each short ton of imported seed contained 17.6 million
infected seed. In 2001, 325,000 tons of
cottonseed were imported into California from Australia. The Australian F.o.v. strain is favored by heavy clay soils and does not require
nematodes for severe disease. Although
the Australian biotypes have not yet been found in California cotton fields, its
presence in imported cottonseed makes it a threat to >4 million acres of
cotton grown on heavy alkaline soils in the U.S. from California to Texas. There is also a treat to U.S. cotton production from highly pathogenic F.o.v. race 4 isolates that have been
identified in California
fields; these attack both Gossypium
barbadense and G. hirsutum cottons,
but the disease is particularly severe on the former. Both the Australian biotype and the California race 4 isolates
produce prodigious quantities of the phytotoxin fusaric acid. This phytotoxin may play a critical role in
the pathogenicity of these pathogens. We
have conducted biosynthetic studies using carbon-13 labelled sodium acetate and
aspartic acid to determine how fusaric acid is synthesized in the pathogen. Results of these studies will be presented.