Association of Fusarium moniliforme with Infection of Sorghum Seedlings by Sclerospora sorghi

1973 ◽  
Vol 63 (1) ◽  
pp. 197 ◽  
Author(s):  
Douglas C. Bain
1994 ◽  
Vol 60 (2) ◽  
pp. 167-174
Author(s):  
Masami YOSHIKAWA ◽  
Norihisa HASHIMOTO ◽  
Tatsuo YOKOYAMA

Crop Science ◽  
1969 ◽  
Vol 9 (6) ◽  
pp. 783-784
Author(s):  
Natale Zummo ◽  
O. H. Coleman ◽  
Billy L. Jones ◽  
R. A. Frederiksen ◽  
A. J. Bockholt

Helia ◽  
2001 ◽  
Vol 24 (34) ◽  
pp. 77-82 ◽  
Author(s):  
Rauf Bhutta ◽  
M.H. Rahber Bhatti ◽  
Ahmad Iftikhar

SUMMARYAll four seed diffusates used for treatment of sunflower seeds, Azadirachtaindica, Capsicum annuum, Coriandrum sativum and Eugenia jambulana, reduced the populations of seed-borne fungi: Alternaria alternata, Drechslera tetramera, Emericellopsis terricola, Fusarium moniliforme, F.semitectum, Macrophomina phaseolina and Phoma oleracea. Of four seed diffusates, those from A.indica and C.sativum controlled the fungal populations almost 100%. Seed germination was increased in seed samples of both sunflower cultivars under study, HO-1 and NK-212. The obtained results indicate that seed diffusates could substitute costly chemicals for safe control of seed-borne diseases, protecting at the same time the environment from chemical pollution.


2021 ◽  
Vol 19 (1) ◽  
Author(s):  
Rong Zhang ◽  
Weitao Jiang ◽  
Xin Liu ◽  
Yanan Duan ◽  
Li Xiang ◽  
...  

Abstract Background Apple replant disease (ARD) has been reported from all major fruit-growing regions of the world, and is often caused by biotic factors (pathogen fungi) and abiotic factors (phenolic compounds). In order to clarify the proteomic differences of Fusarium moniliforme under the action of phloridzin, and to explore the potential mechanism of F. moniliforme as the pathogen of ARD, the role of Fusarium spp. in ARD was further clarified. Methods In this paper, the quantitative proteomics method iTRAQ analysis technology was used to analyze the proteomic differences of F. moniliforme before and after phloridzin treatment. The differentially expressed protein was validated by qRT-PCR analysis. Results A total of 4535 proteins were detected, and 293 proteins were found with more than 1.2 times (P< 0.05) differences. In-depth data analysis revealed that 59 proteins were found with more than 1.5 times (P< 0.05) differences, and most proteins were consistent with the result of qRT-PCR. Differentially expressed proteins were influenced a variety of cellular processes, particularly metabolic processes. Among these metabolic pathways, a total of 8 significantly enriched KEGG pathways were identified with at least 2 affiliated proteins with different abundance in conidia and mycelium. Functional pathway analysis indicated that up-regulated proteins were mainly distributed in amino sugar, nucleotide sugar metabolism, glycolysis/ gluconeogenesis and phagosome pathways. Conclusions This study is the first to perform quantitative proteomic investigation by iTRAQ labeling and LC-MS/MS to identify differentially expressed proteins in F. moniliforme under phloridzin conditions. The results confirmed that F. moniliforme presented a unique protein profile that indicated the adaptive mechanisms of this species to phloridzin environments. The results deepened our understanding of the proteome in F. moniliforme in response to phloridzin inducers and provide a basis for further exploration for improving the efficiency of the fungi as biocontrol agents to control ARD.


1991 ◽  
Vol 266 (22) ◽  
pp. 14486-14490 ◽  
Author(s):  
E. Wang ◽  
W.P. Norred ◽  
C.W. Bacon ◽  
R.T. Riley ◽  
A.H. Merrill

Genetics ◽  
1982 ◽  
Vol 102 (1) ◽  
pp. 19-24
Author(s):  
Sophia Kathariou ◽  
Philip T Spieth

ABSTRACT A Spore killer trait, which exhibits genetic and cytological properties analogous to those previously found in Neurospora, exists in natural populations of the fungal plant pathogen Fusarium moniliforme. The genogeography of the polymorphism in F. moniliforme differs from the situation in Neurospora intermedia. It is more akin to the situation in N. sitophila, although more extreme with respect to the prevalence of killer alleles: more than 80% of tested isolates of F. moniliforme carry the killer allele. Nevertheless, sensitive alleles are widely distributed and have been found in California, Italy, Greece and Central America.


1997 ◽  
Vol 25 (3) ◽  
pp. 375-377
Author(s):  
A. P. Peito ◽  
C. Abrantes ◽  
H. Batalha ◽  
A. M. Fernandes ◽  
I. Felgueiras

Genetics ◽  
1996 ◽  
Vol 143 (1) ◽  
pp. 175-189 ◽  
Author(s):  
Jin-rong Xu ◽  
John F Leslie

Abstract We constructed a recombination-based map of the fungal plant pathogen Gibberella fujikuroi mating population A (asexual stage Fusarium moniliforme). The map is based on the segregation of 142 restriction fragment length polymorphism (RFLP) markers, two auxotrophic genes (arg1, nic1), mating type (matA+ / matA−), female sterility (ste1), spore-killer (Sk), and a gene governing the production of the mycotoxin fumonisin B1 (fum1) among 121 random ascospore progeny from a single cross. We identified 12 linkage groups corresponding to the 12 chromosome-sized DNAs previously observed in contour-clamped homogeneous electric field (CHEF) gels. Linkage groups and chromosomes were correlated via Southern blots between appropriate RFLP markers and the CHEF gels. Eleven of the 12 chromosomes are meiotically stable, but the 12th (and smallest) is subject to deletions in 3% (4/121) of the progeny. Positive chiasma interference occurred on five of the 12 chromosomes, and nine of the 12 chromosomes averaged more than one crossover per chromosome. The average kb/cM ratio in this cross is ~32.


1998 ◽  
Vol 88 (6) ◽  
pp. 550-555 ◽  
Author(s):  
T. K. Cotten ◽  
G. P. Munkvold

The roles of residue size and burial depth were assessed in the survival of Fusarium moniliforme, F. proliferatum, and F. subglutinans in maize stalk residue. Stalk pieces (small or large sizes) were soaked in a spore suspension of F. moniliforme, F. proliferatum, or F. subglutinans and placed in a field on the soil surface or buried at 15- or 30-cm depths. Residue pieces were recovered periodically, cultured on a selective medium, and microscopically examined for the presence of the inoculated Fusarium species. After 630 days, the inoculated Fusarium species were recovered from 0 to 50% of the inoculated stalk pieces in a long-term, continuous maize field, from 0 to 28% of the inoculated stalk pieces placed in a maize/soybean/oat rotation field, and from 0 to 25% of the noninoculated stalk pieces at both locations. Residue size and residue depth had significant effects on survival, but there were significant interactions among strain, depth, residue size, and time. Up to 343 days after placement in the field, survival of the three Fusarium species was not consistently different between buried residues and surface residues, but after 630 days, survival was greater from surface residues. Overall, fungus survival decreased more slowly in the surface residues than in the buried residues. Linear coefficients of determination ranged from 0.35 to 0.82 for the surface residues and from 0.81 to 0.98 for the buried residues. Decline in survival over time followed a more linear pattern in buried residues than in surface residues. Vegetative compatibility tests confirmed that F. moniliforme, F. proliferatum, and F. subglutinans strains can survive at least 630 days in surface or buried maize residue. These results demonstrate that maize residue can act as a long-term source of inoculum for infection of maize plants by these three Fusarium species.


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