scholarly journals Mating Type Distribution and Fertility Status in Magnaporthe grisea Populations from Turfgrasses in Georgia

Plant Disease ◽  
2003 ◽  
Vol 87 (4) ◽  
pp. 435-441 ◽  
Author(s):  
L. P. Tredway ◽  
K. L. Stevenson ◽  
L. L. Burpee
Keyword(s):  
Mating Type ◽  
Tall Fescue ◽  
Magnaporthe Grisea ◽  
Population Analysis ◽  
Low Frequency ◽  
Type Distribution ◽  
Fertility Status ◽  
Polymerase Chain ◽  
Two Populations

Populations of Magnaporthe grisea associated with tall fescue and St. Augustinegrass in Georgia were analyzed for mating type distribution and fertility status in 1999 and 2000. A polymerase chain reaction based assay for mating type was developed to facilitate population analysis. M. grisea populations from St. Augustinegrass in Georgia were dominated by the Mat1-1 mating type, whereas populations from tall fescue were dominated by Mat1-2. The opposite mating type was found in low frequency (0 to 5.7%) associated with each host. The fertility status of isolates from two populations was determined using controlled crosses in vitro. Seventy-eight Mat1-1 isolates from St. Augustinegrass were sterile in test crosses, but a single Mat1-2 isolate from St. Augustinegrass was male fertile. Of 87 Mat1-2 isolates from tall fescue, 47 were male fertile in test crosses, but 19 produced perithecia that were barren. All Mat1-1 isolates from tall fescue were sterile. Although both mating types exist in M. grisea populations from turfgrasses in Georgia, no female fertile isolates were identified in sample populations. The predominance of one mating type in eight sample populations and absence of female fertile isolates in two sample populations indicates that sexual reproduction may not occur with significant frequency in M. grisea populations associated with turfgrasses in Georgia.

scholarly journals Sexually Fertile Magnaporthe grisea Rice Pathogens in Thailand

Plant Disease ◽  
1999 ◽  
Vol 83 (10) ◽  
pp. 939-943 ◽  
Author(s):  
Poonsak Mekwatanakarn ◽  
Wichai Kositratana ◽  
Tawatchai Phromraksa ◽  
R. S. Zeigler
Keyword(s):  
Mating Type ◽  
Male Fertility ◽  
Magnaporthe Grisea ◽  
Female Sterility ◽  
Diverse Populations ◽  
Type Distribution ◽  
Northern Regions ◽  
Rice Pathogens ◽  
Central Thailand

Sexual fertility and mating type distribution of Magnaporthe grisea field isolates collected in Thailand were analyzed from sites previously found to harbor diverse populations of the pathogen. Three hundred forty-one single conidium isolates of M. grisea collected from five sites in north, northeast, and central Thailand were evaluated for in vitro sexual fertility and mating type by pairing with strains of known mating type. Most isolates (67%) were infertile when crossed with the hermaphrodite tester strains; but fertile isolates of each mating type that yielded viable ascospores were detected in all sites from the northeastern and northern regions. MAT1-2 predominated over MAT1-1 in bioassay mating type. Male fertility (female sterility) predominated in fertile MAT1-1 (50 to 75%) and MAT1-2 (50 to 85%) isolates from all locations in Thailand; however, hermaphroditic and/or female fertile isolates were also detected in all but one site. Fertility, as determined by perithecia density, was low (<10 perithecia cm-2) for most isolates, although a few produced in excess of 20 perithecia cm-2.

Mating-type Distribution and Fertility Status in Magnaporthe grisea Populations from Argentina

2005 ◽  
Vol 160 (4) ◽  
pp. 285-290 ◽  
Author(s):  
V. F. Consolo ◽  
C. A. Cordo ◽  
G. L. Salerno
Keyword(s):  
Mating Type ◽  
Magnaporthe Grisea ◽  
Type Distribution ◽  
Fertility Status

scholarly journals Mating Type Distribution and Fertility Status of Magnaporthe grisea Populations from Various Hosts in India

Plant Disease ◽  
1998 ◽  
Vol 82 (1) ◽  
pp. 36-40 ◽  
Author(s):  
G. Viji ◽  
S. S. Gnanamanickam
Keyword(s):  
Mating Type ◽  
Magnaporthe Grisea ◽  
Finger Millet ◽  
Mendelian Inheritance ◽  
Mating Types ◽  
Type Distribution ◽  
Fertility Status ◽  
Indian Isolates ◽  
Brachiaria Mutica

Production of perithecia, asci, and ascospores by Indian isolates of Magnaporthe grisea is rare and has not been found among the Southern Indian isolates of the blast pathogen. From among 138 monoconidial isolates that infect rice and other hosts, we now report the distribution of mating types (MAT1-1 and MAT1-2) of M. grisea in finger millet and paragrass (Brachiaria mutica)-infecting isolates. Twenty-eight of the 96 finger millet isolates, 5 of the 16 paragrass isolates, and none of the 26 rice isolates produced fertile perithecia in laboratory matings with fertile testers. Backcrosses of ascospore progenies to the parental M. grisea isolate but not to the tester strain resulted in fertile perithecial formation, and a further backcrossing scheme indicated definite fertility patterns of Mendelian inheritance in M. grisea.

scholarly journals In Vitro Activity of S-3578, a New Broad-Spectrum Cephalosporin Active against Methicillin-Resistant Staphylococci

2003 ◽  
Vol 47 (3) ◽  
pp. 923-931 ◽  
Author(s):  
Takaji Fujimura ◽  
Yoshinori Yamano ◽  
Isamu Yoshida ◽  
Jingoro Shimada ◽  
Shogo Kuwahara
Keyword(s):  
Antibacterial Activity ◽  
Population Analysis ◽  
Low Frequency ◽  
Methicillin Resistant ◽  
Gram Positive Bacteria ◽  
Highly Active ◽  
In Vitro Antibacterial Activity ◽  
Mrsa Strains ◽  
Time Kill

ABSTRACT The in vitro antibacterial activity of S-3578, a new parenteral cephalosporin, against clinical isolates was evaluated. The MICs of the drug at which 90% of the isolates were inhibited were 4 μg/ml for methicillin-resistant Staphylococcus aureus (MRSA) and 2 μg/ml for methicillin-resistant Staphylococcus epidermidis, which were fourfold higher than and equal to those of vancomycin, respectively. The anti-MRSA activity of S-3578 was considered to be due to its high affinity for penicillin-binding protein 2a (50% inhibitory concentration, 4.5 μg/ml). In time-kill studies with 10 strains each of MRSA and methicillin-susceptible S. aureus, S-3578 caused more than a 4-log10 decrease of viable cells on the average at twice the MIC after 24 h of exposure, indicating that it had potent bactericidal activity. Furthermore, in population analysis of MRSA strains with heterogeneous or homogeneous resistance to imipenem, no colonies emerged from about 109 cells on agar plates containing twice the MIC of S-3578, suggesting the low frequency of emergence of S-3578-resistant strains from MRSA. S-3578 was also highly active against penicillin-resistant Streptococcus pneumoniae (PRSP), with a MIC90 of 1 μg/ml, which was comparable to that of ceftriaxone. S-3578 also had antibacterial activity against a variety of gram-negative bacteria including Pseudomonas aeruginosa, though its activity was not superior to that of cefepime. In conclusion, S-3578 exhibited a broad antibacterial spectrum and, particularly, had excellent activity against gram-positive bacteria including methicillin-resistant staphylococci and PRSP. Thus, S-3578 was considered to be worthy of further evaluation.

scholarly journals Mating-Type Gene Structure and Spatial Distribution of Didymella tanaceti in Pyrethrum Fields

2016 ◽  
Vol 106 (12) ◽  
pp. 1521-1529 ◽  
Author(s):  
Tamieka L. Pearce ◽  
Jason B. Scott ◽  
Frank S. Hay ◽  
Sarah J. Pethybridge
Keyword(s):  
Spatial Distribution ◽  
Mating Type ◽  
Tan Spot ◽  
Mating Types ◽  
Tanacetum Cinerariifolium ◽  
Polymerase Chain ◽  
Type Gene ◽  
Mat Genes

Tan spot of pyrethrum (Tanacetum cinerariifolium) is caused by the ascomycete Didymella tanaceti. To assess the evolutionary role of ascospores in the assumed asexual species, the structure and arrangement of mating-type (MAT) genes were examined. A single MAT1-1 or MAT1-2 idiomorph was identified in all isolates examined, indicating that the species is heterothallic. The idiomorphs were flanked upstream and downstream by regions encoding pyridoxamine phosphate oxidase-like and DNA lyase-like proteins, respectively. A multiplex MAT-specific polymerase chain reaction assay was developed and used to genotype 325 isolates collected within two transects in each of four fields in Tasmania, Australia. The ratio of isolates of each mating-type in each transect was consistent with a 1:1 ratio. The spatial distribution of the isolates of the two mating-types within each transect was random for all except one transect for MAT1-1 isolates, indicating that clonal patterns of each mating-type were absent. However, evidence of a reduced selection pressure on MAT1-1 isolates was observed, with a second haplotype of the MAT1-1-1 gene identified in 4.4% of MAT1-1 isolates. In vitro crosses between isolates with opposite mating-types failed to produce ascospores. Although the sexual morph could not be induced, the occurrence of both mating-types in equal frequencies suggested that a cryptic sexual mode of reproduction may occur within field populations.

Mating type distribution using a multiplex PCR mating assay and fertility status inDidymella rabieiin chickpea-growing areas in Iran

2014 ◽  
Vol 47 (9) ◽  
pp. 1030-1041
Author(s):  
Farshid Mahmodi ◽  
Ziaeddin Banihashemi ◽  
Jugah Kadir ◽  
Adam Puteh ◽  
Abbas Nasehi
Keyword(s):  
Multiplex Pcr ◽  
Mating Type ◽  
Type Distribution ◽  
Fertility Status

scholarly journals Distribution of Mating Type Alleles and Fertility Status of Magnaporthe grisea Causing Gray Leaf Spot of Perennial Ryegrass and St. Augustinegrass Turf

Plant Disease ◽  
2002 ◽  
Vol 86 (8) ◽  
pp. 827-832 ◽  
Author(s):  
G. Viji ◽  
W. Uddin
Keyword(s):  
Mating Type ◽  
Perennial Ryegrass ◽  
Leaf Spot ◽  
Magnaporthe Grisea ◽  
Finger Millet ◽  
Gray Leaf Spot ◽  
Pathogen Population ◽  
Fertility Status ◽  
Single Location ◽  
Single Mating

Isolates of Magnaporthe grisea causing gray leaf spot of perennial ryegrass (PR) (Lolium perenne) and St. Augustinegrass (SA) (Stenotaphrum secundatum) were analyzed for mating compatibility and fertility. A total of 312 isolates of M. grisea from PR and 62 isolates from SA were paired with hermaphroditic tester strains from finger millet (Eleusine coracana), rice (Oryza sativa), and wheat (Triticum aestivum). All the PR isolates belonged to a single mating type, MAT1-2. Male fertility was observed in all these isolates. Asci and ascospores were not produced regardless of their developmental stage. Of the 139 (44.6%) isolates from PR that formed perithecia with the fertile tester strains, 83 (59.7%) were highly fertile, 33 (23.7%) were intermediately fertile, and 23 (16.5%) were low in fertility. Both mating types were observed among the isolates of SA, where MAT1-1 predominated the MAT1-2 type. An equal number of male and female fertile isolates were detected among these isolates obtained from a single location; however, none of the isolates behaved as hermaphrodites. Few ascospores were produced in crosses between two isolates of SA and a finger millet tester. Of the 62 monoconidial isolates of SA tested, 19 (30.6%) isolates formed perithecia, of which 5 (26.3%) were highly fertile, 7 (36.8%) were intermediately fertile, 7 (36.8%) were low in fertility, and 43 (69.4%) were infertile. The results of this study indicate that the sexual stage may not be a significant factor contributing to the genetic variation the gray leaf spot pathogen population.

scholarly journals Rapid Population Analysis of Magnaporthe grisea by Using rep-PCR and Endogenous Repetitive DNA Sequences

1998 ◽  
Vol 88 (3) ◽  
pp. 223-229 ◽  
Author(s):  
M. L. C. George ◽  
R. J. Nelson ◽  
R. S. Zeigler ◽  
H. Leung
Keyword(s):  
Dna Sequences ◽  
Large Scale ◽  
Magnaporthe Grisea ◽  
Population Analysis ◽  
Low Cost ◽  
Genetic Relationships ◽  
Fungal Genome ◽  
Scale Population ◽  
Polymerase Chain ◽  
The Impact

DNA samples from Magnaporthe grisea isolates were fingerprinted by using repetitive element-based polymerase chain reaction (rep-PCR) with two outwardly directed primer sequences from Pot2, an element found in approximately 100 copies in the fungal genome. Variable length fragments, defining the sequences lying between these elements, were generated, and fingerprint patterns specific for individual strains were established. “Long PCR” conditions, including higher pH (9.2) and increased extension time (10 min) were used to amplify DNA fragments ranging from 400 bp to longer than 23 kb. Polymorphisms specific to M. grisea strains were generated, allowing inference of their genetic relationships. Segregation analysis was used to confirm single-locus inheritance for the fragments amplified by rep-PCR. Cluster analysis revealed robust groupings that corresponded to previously determined MGR586 restriction fragment length polymorphism lineages of the rice-infecting strains of the pathogen. We have also demonstrated the utility of rep-PCR to differentiate isolates that infect rice from those that infect nonrice hosts. DNA fingerprinting by Pot2 rep-PCR provides an efficient means to monitor the population dynamics of the blast pathogen. Because of the method's low cost and ease in application, it is now feasible to conduct large-scale population studies to understand the impact of host genotypes on pathogen evolution.

Characterization of the Original Christmas Disease Mutation (Cysteine 206 → Serine): From Clinical Recognition to Molecular Pathogenesis

1992 ◽  
Vol 67 (01) ◽  
pp. 063-065 ◽  
Author(s):  
Sherryl A M Taylor ◽  
Jacalyn Duffin ◽  
Cherie Cameron ◽  
Jerome Teitel ◽  
Bernadette Garvey ◽  
...  
Keyword(s):  
Nucleotide Substitution ◽  
Novel Mutation ◽  
Factor Ix ◽  
Causative Mutation ◽  
Coding Region ◽  
Body Of Knowledge ◽  
Polymerase Chain ◽  
Splice Junctions

SummaryChristmas disease was first reported as a distinct clinical entity in two manuscripts published in 1952 (1, 2). The eponym associated with this disorder, is the surname of the first patient examined in detail and reported by Biggs and colleagues in a paper describing the clinical and laboratory features of seven affected individuals (3). This patient has severe factor IX coagulant deficiency (less than 0.01 units/ml) and no detectable circulating factor IX antigen (less than 0.01 units/ml). Coding sequence and splice junctions of the factor IX gene from this patient have been amplified in vitro through the polymerase chain reaction (PCR). One nucleotide substitution was identified at nucleotide 30,070 where a guanine was replaced by a cytosine. This mutation alters the amino acid encoded at position 206 in the factor IX protein from cysteine to serine. The non conservative nature of this substitution, the absence of this change in more than 200 previously sequenced factor IX genes and the fact that the remainder of the coding region of this gene was normal, all provide strong circumstantial evidence in favour of this change being the causative mutation in this patient. The molecular characterization of this novel mutation in the index case of Christmas disease, contributes to the rapidly expanding body of knowledge pertaining to Christmas disease pathogenesis.

Triploidy in a Live-Born Extremely Low Birth Weight Twin: Clinical Aspects

2020 ◽  
Author(s):  
Liliya Vakrilova ◽  
Stanislava Hitrova-Nikolova ◽  
Irena Bradinova
Keyword(s):  
Left Lung ◽  
Extremely Low Birth Weight ◽  
Clinical Aspects ◽  
Severe Respiratory Distress ◽  
Vitro Fertilization ◽  
Gestational Week ◽  
Polymerase Chain ◽  
Fluorescent Polymerase Chain Reaction ◽  
Second Twin

AbstractTriploidy is a rare chromosomal aberration characterized by a karyotype with 69 chromosomes. Triploid fetuses usually are miscarried in early pregnancy. We present a case of a triploid twin and a genetically unaffected co-twin, conceived through in vitro fertilization. A discordant growth was registered at 20 weeks of gestation. Cesarean section was performed at 355/7 gestational week. The second twin was extremely growth restricted female (780 g) with oligohydramnios and severe respiratory distress, and died at 20 hours of age. The autopsy revealed unilobar left lung, bilobar right lung, and cysts of the terminal bronchioles. Quantitative fluorescent polymerase chain reaction detected triploidy compatible pattern. So, early intrauterine growth restriction may be a sign of triploidy, which must be proven by pre or postnatal genetic testing.

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