Genetics, Vol. 159, 107-118, September 2001, Copyright © 2001

Genetic Control of Horizontal Virus Transmission in the Chestnut Blight Fungus, Cryphonectria parasitica

Paolo Cortesia, Charles E. McCullochb, Haiyue Songb, Haiqun Linb, and Michael G. Milgroomc
a Istituto di Patologia Vegetale, Università degli Studi di Milano, 20133 Milan, Italy,
b Departments of Statistical Science and Biometrics, Cornell University, Ithaca, New York 14853
c Department of Plant Pathology, Cornell University, Ithaca, New York 14853

Corresponding author: Michael G. Milgroom, Department of Plant Pathology, Cornell University, 334 Plant Science Bldg., Ithaca, NY 14853-4203., mgm5{at}cornell.edu (E-mail)

Communicating editor: R. H. DAVIS

Vegetative incompatibility in fungi has long been known to reduce the transmission of viruses between individuals, but the barrier to transmission is incomplete. In replicated laboratory assays, we showed conclusively that the transmission of viruses between individuals of the chestnut blight fungus Cryphonectria parasitica is controlled primarily by vegetative incompatibility (vic) genes. By replicating vic genotypes in independent fungal isolates, we quantified the effect of heteroallelism at each of six vic loci on virus transmission. Transmission occurs with 100% frequency when donor and recipient isolates have the same vic genotypes, but heteroallelism at one or more vic loci generally reduces virus transmission. Transmission was variable among single heteroallelic loci. At the extremes, heteroallelism at vic4 had no effect on virus transmission, but transmission occurred in only 21% of pairings that were heteroallelic at vic2. Intermediate frequencies of transmission were observed when vic3 and vic6 were heteroallelic (76 and 32%, respectively). When vic1, vic2, and vic7 were heteroallelic, the frequency of transmission depended on which alleles were present in the donor and the recipient. The effect of heteroallelism at two vic loci was mostly additive, although small but statistically significant interactions (epistasis) were observed in four pairs of vic loci. A logistic regression model was developed to predict the probability of virus transmission between vic genotypes. Heteroallelism at vic loci, asymmetry, and epistasis were the dominant factors controlling transmission, but host genetic background also was statistically significant, indicating that vic genes alone cannot explain all the variation in virus transmission. Predictions from the logistic regression model were highly correlated to independent transmission tests with field isolates. Our model can be used to estimate horizontal transmission rates as a function of host genetics in natural populations of C. parasitica.





This article has been cited by other articles:


Home page
MycologiaHome page
N. D. Charlton and M. A. Cubeta
Transmission of the M2 double-stranded RNA in Rhizoctonia solani anastomosis group 3 (AG-3).
Mycologia, November 1, 2007; 99(6): 859 - 867.
[Abstract] [Full Text] [PDF]


Home page
MycologiaHome page
Y.-C. Liu and M. G. Milgroom
High diversity of vegetative compatibility types in Cryphonectria parasitica in Japan and China
Mycologia, March 1, 2007; 99(2): 279 - 284.
[Abstract] [Full Text] [PDF]


Home page
Eukaryot CellHome page
K. Dementhon, G. Iyer, and N. L. Glass
VIB-1 Is Required for Expression of Genes Necessary for Programmed Cell Death in Neurospora crassa
Eukaryot. Cell, December 1, 2006; 5(12): 2161 - 2173.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
C. O. Micali and M. L. Smith
A Nonself Recognition Gene Complex in Neurospora crassa
Genetics, August 1, 2006; 173(4): 1991 - 2004.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
I. Kaneko, K. Dementhon, Q. Xiang, and N. L. Glass
Nonallelic Interactions Between het-c and a Polymorphic Locus, pin-c, Are Essential for Nonself Recognition and Programmed Cell Death in Neurospora crassa.
Genetics, March 1, 2006; 172(3): 1545 - 1555.
[Abstract] [Full Text] [PDF]


Home page
MycologiaHome page
M. L. Smith, C. C. Gibbs, and M. G. Milgroom
Heterokaryon incompatibility function of barrage-associated vegetative incompatibility genes (vic) in Cryphonectria parasitica.
Mycologia, January 1, 2006; 98(1): 43 - 50.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
I. Carbone, Y.-C. Liu, B. I. Hillman, and M. G. Milgroom
Recombination and Migration of Cryphonectria hypovirus 1 as Inferred From Gene Genealogies and the Coalescent
Genetics, April 1, 2004; 166(4): 1611 - 1629.
[Abstract] [Full Text] [PDF]


Home page
MicrobiologyHome page
A. L. Dawe, V. C. McMains, M. Panglao, S. Kasahara, B. Chen, and D. L. Nuss
An ordered collection of expressed sequences from Cryphonectria parasitica and evidence of genomic microsynteny with Neurospora crassa and Magnaporthe grisea
Microbiology, September 1, 2003; 149(9): 2373 - 2384.
[Abstract] [Full Text] [PDF]


Home page
Appl. Environ. Microbiol.Home page
P. J. Hoegger, U. Heiniger, O. Holdenrieder, and D. Rigling
Differential Transfer and Dissemination of Hypovirus and Nuclear and Mitochondrial Genomes of a Hypovirus-Infected Cryphonectria parasitica Strain after Introduction into a Natural Population
Appl. Envir. Microbiol., July 1, 2003; 69(7): 3767 - 3771.
[Abstract] [Full Text] [PDF]


Home page
Eukaryot CellHome page
N. L. Glass and I. Kaneko
Fatal Attraction: Nonself Recognition and Heterokaryon Incompatibility in Filamentous Fungi
Eukaryot. Cell, February 1, 2003; 2(1): 1 - 8.
[Full Text] [PDF]