scholarly journals Phytophthora infestans Mating Types on Tomato (Solanum lycopersicum) in Southern Spain

Plant Disease ◽  
2007 ◽  
Vol 91 (1) ◽  
pp. 109-109 ◽  
Author(s):  
J. M. Segura ◽  
M. de Cara ◽  
M. Santos ◽  
J. Tello

During 2004, an unusual spread of Phytophthora infestans on tomato plants in greenhouses located in Almería and Granada provinces, southern Spain, was observed. Infected plants had water-soaked, brown spots on leaves and stems and necrotic areas with white mold on the surface of fruits. Three isolates were obtained by plating diseased tissue on V8 juice agar medium and maintained on rye agar at 18°C. These isolates were analyzed for the mating type. Crosses were carried out using V8 juice agar and rye agar. The two parental isolates US1 (A1) and US8 (A2) were both provided by W. E. Fry, Cornell University, Ithaca, NY. Two of the Spanish isolates were homothallic and the other isolate belonged to the uncommon mating type A1A2. To confirm the occurrence of the two mating types, 43 single-sporangium progeny were produced and analyzed from the A1A2 mating type. Thirty eight isolates were A1, two were A2, one was A1A2 mating type, and two were sterile. Assessment of five single-sporangium progeny from the homothallic type resulted in two A1, two homothallic, and one sterile isolate. A1A2 isolates produced oospores when crossed with either A1 or A2, but not when self-crossed. Previously, the A1A2 mating type has been found in Israel in the field and was obtained from oospores produced on tomato seeds (2,3). Since 2003, mating types of P. infestans isolates recovered from potato (60) and tomato (8) in southern Spain have been characterized. Seventy-five percent of the isolates recovered from potato were A1 and 25% were A2 mating types. Isolates recovered from tomato were 50% A1 and 50% A2 (1). To our knowledge, this is the first report of the occurrence of the A1A2 mating type and homothallic P. infestans isolates on tomato in Spain. References: (1) E. Andujar et al. Congr. Sociedad Española de Fitopatol. 12:244, 2004. (2) E. Rubin and Y. Cohen. Phytoparasitica 32:237, 2004. (3) E. Rubin and Y. Cohen. Plant Dis. 90:741, 2006.

2013 ◽  
Vol 55 (1) ◽  
pp. 389-400 ◽  
Author(s):  
Hanna Zarzycka ◽  
Sylwester Sobkowiak ◽  
Renata Lebecka ◽  
Beata Tatarowska

The formation of phenotypic structure of <i>P.infestans</i> population in Poland was determined by analyzing 1603 isolates collected from 1987 to 2001. The race complexity, low at the beginning of experiment, has been increasing from year to year and reached in 2001 a high level 7,2 virulence factors per isolate. The single and less composed races dominating firstly in the population were replaced gradually by more composed races. The virulence factors 1, 2, 3, 4, 7 and 11 occurred most frequently, but factors 5 and 8 were noted sporadically. The A2 mating type was detected in 1988 at first and since that time its occurrence has been noted in Polish population each year. The oospores were formed in potato tissues. Race diversity, low at the beginning of the investigation, reached a peak in 1996-2001 . During 1987-1990 weakly and middly aggressive phenotypes dominated in Polish population. In the later period very aggressive isolates were more frequent. Phenotypic race similarity of <i>P.infestans</i> populations in 1987 and 2001 was very low. The race structure of 1987 population was totally different from the race structure of populations of the next years. It was probably due to migration of new pathotypes. On the other hand the variation in complexity, diversity and similarity of races, as well as in aggressiveness observed in later years of investigation can be caused by the presence of both mating types and sexual recombination.


1983 ◽  
Vol 61 (5) ◽  
pp. 1462-1466 ◽  
Author(s):  
Chong-Yao Shen ◽  
Leslie A. Bower ◽  
Donald C. Erwin ◽  
Peter H. Tsao

Oogonia with attached antheridia, many of which contained mature thick-walled oospores, were formed in the A1 mating type of Phytophthora infestans after it had been paired with the A2 mating type of P. parasitica, P. palmivora, P. capsici, or P. infestans, on opposite sides of a polycarbonate membrane. The A2 culture discs, in both top and bottom positions in relation to the polycarbonate membrane, induced sex-organ formation in the A1 isolate of P. infestans. Sex organs were formed in P. infestans at 12, 15, 18, 21, and 24 °C, but they were most abundant at 15 and 18 °C and least at 24 °C. More sex organs in the P. infestans A1 isolate were induced by three A2 isolates of P. parasitica than by an A2 isolate of P. infestans. Evidence was presented that a diffusible oospore-inducing substance was produced by the A2 isolate of P. parasitica in the agar medium even when the A1 isolate of P. infestans was absent on the other side of the membrane. Because both P. infestans and P. parasitica are pathogenic to tomato and potato, such interspecific induction of the formation of selfed oospores in the A1 mating type of P. infestans could play an important role in survival and variation of P. infestans throughout the world.


Genetics ◽  
1995 ◽  
Vol 141 (2) ◽  
pp. 503-512 ◽  
Author(s):  
H S Judelson ◽  
L J Spielman ◽  
R C Shattock

Abstract DNA markers linked to the determinants of mating type in the oomycete, Phytophthora infestans, were identified and used to address the genetic basis of heterothallism in the normally diploid fungus. Thirteen loci linked to the A1 and A2 mating types were initially identified by bulked segregant analysis using random amplified polymorphic DNA markers (RAPDs) and subsequently scored in three crosses polymorphisms (SSCP), cleaved amplified polymorphisms (CAPS), or allele-specific polymerase chain reaction markers (AS-PCR). All DNA markers mapped to a single region, consistent with a single locus determining both mating types. Long-range restriction mapping also demonstrated the linkage of the markers to one region and delimited the mating type locus to a 100-kb region. The interval containing the mating type locus displayed non-Mendelian segregation as only two of the four expected genotypes were detected in progeny. This is consistent with a system of balance lethal loci near the mating type locus. A model for mating type determination is presented in which the balanced lethals exclude form progeny those with potentially conflicting combinations of mating type alleles, such as those simultaneously expressing A1 and A2 functions.


2010 ◽  
Vol 42 (No. 2) ◽  
pp. 41-48 ◽  
Author(s):  
J. Mazáková ◽  
V. Táborský ◽  
M. Zouhar ◽  
P. Ryšánek ◽  
E. Hausvater ◽  
...  

A total of 199 <i>Phytophthora infestans</i> isolates were obtained from leaves, tubers and fruits of infected crops of potato and tomato in different regions of the Czech Republic in 2003, 2004 and 2005. They were analysed for mating type using the conventional pairing assay and PCR markers; 107 isolates were of A1 and 92 of A2 mating type. No self-fertile isolate was found. Our study is the first report of the presence and distribution of the A2 mating type of <i>P. infestans</i> in the Czech Republic. The co-existence of the two mating types may enable the pathogen to reproduce sexually, thus enhancing the diversity of its population countrywide.


Genetics ◽  
1991 ◽  
Vol 128 (3) ◽  
pp. 539-547 ◽  
Author(s):  
M Picard ◽  
R Debuchy ◽  
E Coppin

Abstract DNAs that encode the mating-type functions (mat+ and mat-) of the filamentous fungus Podospora anserina were cloned with the use of the mating-type A probe from Neurospora crassa. Cloning the full mat information was ascertained through gene replacement experiments. Molecular and functional analyses of haploid transformants carrying both mating types lead to several striking conclusions. Mat+ mat- strains are dual maters. However, the resident mat information is dominant to the mat information added by transformation with respect to fruiting body development and ascus production. Moreover, when dual mating mat+ mat- strains are crossed to mat+ or mat- testers, there is strong selection, after fertilization, that leads to the loss from the mat+ mat- nucleus of the mat information that matches that of the tester. Finally, the mat locus contains at least two domains, one sufficient for fertilization, the other necessary for sporulation.


Plant Disease ◽  
2000 ◽  
Vol 84 (2) ◽  
pp. 173-176 ◽  
Author(s):  
M. Sedegui ◽  
R. B. Carroll ◽  
A. L. Morehart ◽  
T. A. Evans ◽  
S. H. Kim ◽  
...  

ABSRACT In 1996 to 1998, a late-blight survey was conducted in potato- and tomato-growing regions of Morocco. A total of 149 isolates of Phytophthora infestans were collected and analyzed for the glucose-6-phosphate isomerase (Gpi) and peptidase (Pep) alleles, mating types, and metalaxyl sensitivities. Four genotypes were identified: MO-1 (mating type A1, Gpi 100/100, Pep 92/100), MO-2 (mating type A1, Gpi 86/100, Pep 92/100), MO-3 (mating type A2 Gpi 100/100, Pep 100/100), and MO-4 (mating type A1, Gpi 100/100, Pep 100/100). The potato isolates were MO-1 (1996 & 97), MO-3 (1998), and MO-4 (1998). The frequencies of A1 (MO-4) and A2 (MO-3) mating types in potato fields in 1998 were 26 and 74%, respectively. Potato isolates were pathogenic to both potatoes and tomatoes. The isolates collected from tomatoes in 1997 and 1998 were MO-2. Potato and tomato isolates were insensitive and sensitive to metalaxyl, respectively. The change of genotype population in 1998 was probably caused by migration of a new genotype from Europe associated with importation of potato seed. The detection of A1 and A2 mating types in the same potato field indicates the potential for sexual reproduction of P. infestans in Morocco.


Plant Disease ◽  
2003 ◽  
Vol 87 (8) ◽  
pp. 896-900 ◽  
Author(s):  
Ailton Reis ◽  
Christine D. Smart ◽  
William E. Fry ◽  
Luiz A. Maffia ◽  
Eduardo S. G. Mizubuti

The population of Phytophthora infestans in Brazil was first characterized 12 years ago. In this research, isolates of P. infestans from potato (n = 184) and tomato (n = 267) collected in southern and southeastern Brazil were characterized to provide more detailed analysis of the current structure of the population. All 451 isolates were analyzed for mating type, and subsets of the isolates were analyzed for allozymes, restriction fragment length polymorphism fingerprint, mtDNA haplotypes, and metalaxyl resistance. Tomato isolates were all of A1 mating type, mtDNA Ib, and US-1 genotype or some variant within this clonal lineage. Of the potato isolates, 82% were A2 mating type, mtDNA IIa, BR-1 genotype, which is a new lineage of P. infestans. All A2 isolates were found on potato, whereas 91% of the A1 isolates were from tomato. A1 and A2 isolates were never found in the same field. The frequency of resistance to metalaxyl was higher in isolates from tomato (55%) than in isolates from potato (38%). After more than a decade of coexistence of isolates of the A1 and A2 mating types, the population was highly clonal, dominated by the BR-1 and US-1 clonal lineages.


2013 ◽  
Vol 12 (7) ◽  
pp. 1033-1038 ◽  
Author(s):  
Gabriela Rodríguez-Arellanes ◽  
Carolina Nascimento de Sousa ◽  
Mauro de Medeiros-Muniz ◽  
José A. Ramírez ◽  
Cláudia V. Pizzini ◽  
...  

ABSTRACTTheMAT1-1andMAT1-2idiomorphs associated with theMAT1locus ofHistoplasma capsulatumwere identified by PCR. A total of 28 fungal isolates, 6 isolates from human clinical samples and 22 isolates from environmental (infected bat and contaminated soil) samples, were studied. Among the 14 isolates from Mexico, 71.4% (95% confidence interval [95% CI], 48.3% to 94.5%) were of theMAT1-2genotype, whereas 100% of the isolates from Brazil were of theMAT1-1genotype. EachMAT1idiomorphic region was sequenced and aligned, using the sequences of the G-217B (+ mating type) and G-186AR (− mating type) strains as references. BLASTn analyses of theMAT1-1andMAT1-2sequences studied correlated with their respective + and − mating type genotypes. Trees were generated by the maximum likelihood (ML) method to search for similarity among isolates of eachMAT1idiomorph. AllMAT1-1isolates originated from Brazilian bats formed a well-defined group; three isolates from Mexico, the G-217B strain, and a subgroup encompassing all soil-derived isolates and two clinical isolates from Brazil formed a second group; last, one isolate (EH-696P) from a migratory bat captured in Mexico formed a third group of theMAT1-1genotype. TheMAT1-2idiomorph formed two groups, one of which included twoH. capsulatumisolates from infected bats that were closely related to the G-186AR strain. The other group was formed by two human isolates and six isolates from infected bats. Concatenated ML trees, with internal transcribed spacer 1 (ITS1) -5.8S-ITS2 andMAT1-1orMAT1-2sequences, support the relatedness ofMAT1-1orMAT1-2isolates.H. capsulatummating types were associated with the geographical origin of the isolates, and all isolates from Brazil correlated with their environmental sources.


2021 ◽  
Author(s):  
George W. A. Constable ◽  
Hanna Kokko

Recently, it was pointed out (Lehtonen et al., 2021) that classic models for the evolution of anisogamy do not take into account the possibility of parthenogenetic reproduction, even though sex is facultative in many relevant taxa (e.g. algae) that harbour both anisogamous and isogamous species. Here we complement the analysis of (Lehtonen et al., 2021) with an approach where we assume that the relationship between progeny size and its survival may differ between parthenogenetically and sexually produced progeny, favouring either the former or the latter. We show that the findings of (Lehtonen et al., 2021), that parthenogenesis can stabilise isogamy relative to the obligate sex case, extend to our scenarios. We additionally investigate two different ways for one mating type to take over the entire population. First, parthenogenesis can lead to biased sex ratios that are sufficiently extreme that one type can displace the other, leading to de facto asexuality for the remaining type that now lacks partners to fuse with. This process involves positive feedback: microgametes, being numerous, lack opportunities for syngamy, and should they proliferate parthenogenetically, the next generation makes this asexual route even more prominent for microgametes. Second, we consider mutations to strict asexuality in producers of micro- or macrogametes, and show that the prospects of asexual invasion depend strongly on the mating type in which the mutation arises. Perhaps most interestingly, we also find scenarios in which parthenogens have an intrinsic survival advantage yet facultatively sexual isogamous populations are robust to the invasion of asexuals, despite us assuming no genetic benefits of recombination. Here equal contribution from both mating types to zygotes that are sufficiently well provisioned to outweigh the additional costs associated with syngamy.


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