A reciprocal translocation and possible insertion(s) tightly associated with host-specific virulence in Cochliobolus heterostrophus

Genome ◽  
1996 ◽  
Vol 39 (3) ◽  
pp. 549-557 ◽  
Author(s):  
Hsin-Ru Chang ◽  
Charlotte R. Bronson

A reciprocal translocation and one or more apparent insertions are shown to be tightly associated with Tox1, a locus controlling T-toxin production and host-selective virulence in race T of the maize pathogen Cochliobolus heterostrophus. Chromosome arrangements were examined by separating chromosomal DNAs of a variety of Tox+ and Tox− strains by pulsed-field gel electrophoresis and hybridizing with probes known to detect RFLPs genetically linked to Tox1. The existence of the translocation was demonstrated by chromosome hybridization patterns; the existence of the putative insertion(s) was deduced from chromosome migration rates. Both differences in chromosome arrangement were detected between 8 Tox+ and 8 Tox− near-isogenic laboratory strains, suggesting that the differences are tightly linked to Tox1. The reciprocal translocation was also detected between all 7 Tox+ and 8 Tox− field isolates examined, suggesting that the translocation is common in natural populations. The field isolates may also differ by the insertion(s); however, numerous additional chromosome size polymorphisms in the field isolates prevented a firm conclusion. The tight association of the translocation and insertion(s) with T-toxin production suggests that chromosome rearrangements may have been involved in the evolution of race T and Tox1. These genomic differences may be causally related to the previously reported reduced fitness of race T relative to race O on N-cytoplasm maize. Key words : chromosome rearrangement, southern corn leaf blight, pulsed-field electrophoresis, T-toxin, evolution.

Genome ◽  
1988 ◽  
Vol 30 (1) ◽  
pp. 12-18 ◽  
Author(s):  
Charlotte R. Bronson

Crosses heterozygous for the virulence locus Tox1 show a high frequency of nonrandom ascospore abortion, in addition to a high frequency of random abortion seen in homozygous crosses. In crosses among closely related laboratory strains, the frequency of asci with eight mature, viable spores dropped from 35–47% of asci with mature spores in crosses homozygous for Tox1 to 3–17% in heterozygous crosses. Segregation for alternate alleles of Tox1 was 2:2 in 98% of asci with four viable spores. Patterns of abortion in crosses involving field isolates were similar to the patterns in crosses among laboratory strains. No recombinants between Tox1 and the abortion-inducing factor were detected among 112 progeny of laboratory strains. The results suggest that race T (TOX1) and race O (tox1) strains of C. heterostrophus differ by a chromosome rearrangement, possibly a reciprocal translocation, with a breakpoint at or near Tox1.Key words: fertility, T-toxin, Cochliobolus heterostrophus, Helminthosporium maydis, Bipolaris maydis, Drechslera maydis, chromosome rearrangement, reciprocal translocation.


1992 ◽  
Vol 109 (3) ◽  
pp. 413-421 ◽  
Author(s):  
W. Witte ◽  
H. Grimm

SUMMARYAmong 63Staphylococcus aureusisolates (one isolate per one patient) counted from infections (from August to November 1991) in hospital T., eight exhibited resistance to fluoroquinolones. Seven of these quinolone-resistant isolates were multiply- and methicillin-resistantS. aureus(QR-MRSA). The results of phage-, plasmid- and genotyping (pulsed field electrophoresis) revealed that six different strain-clones of these MRSA were spread in the hospital.In vitrospontaneous mutants resistant to fluoroquinolones are 1–-100-fold more frequent in MRSA than in otherS. aureuswhen selected on isosensitest-agar containing 1 μg/ml of ciprofloxacin. However, the same mutant frequencies were found in strain 8325–4 with and without the mecA-determinant. The resistance phenotype was stable over 30 generations of subculture in nutrient broth as well in natural quinolone resistant MRSA as in mutants of other types ofS.aureusselectedin vitro. The phenotypic association of quinolone resistance and MRSA is rather likely due to a higher frequency of spontaneous resistant mutants which are present in natural populations of MRSA. Data of chemotherapy prior to the isolation of 8. aureus show that three of seven patients from whom QR-MRSA were isolated were treated with a quinolone. In eight cases of infections with non-MRSA and quinolone treatment the isolatedS. aureusstrains werein vitrosensitive to quinolones.


Genetics ◽  
1999 ◽  
Vol 151 (2) ◽  
pp. 585-596 ◽  
Author(s):  
M Kodama ◽  
M S Rose ◽  
G Yang ◽  
S H Yun ◽  
O C Yoder ◽  
...  

Abstract Previously, Tox1 was defined as a single genetic element controlling the difference between races of Cochliobolus heterostrophus: race T is highly virulent on T-cytoplasm corn and produces the polyketide T-toxin; race O is weakly virulent and does not produce T-toxin. Here we report that Tox1 is two loci, Tox1A and Tox1B, on two different chromosomes. Evidence for two loci derives from: (1) the appearance of 25% Tox+ progeny in crosses between induced Tox1– mutants, one defective at Tox1A, the other at Tox1B; (2) the ability of Tox1A– + Tox1B– heterokaryons to complement for T-toxin production; and (3) electrophoretic karyotypes proving that Tox1– mutations are physically located on two different chromosomes. Data showing Tox1 as a single genetic element are reconciled with those proving it is two loci by the fact that Tox1 is inseparably linked to the breakpoints of a reciprocal translocation; the translocation results in a four-armed linkage group. In crosses where the translocation is heterozygous (i.e., race T by race O), all markers linked to the four-armed intersection appear linked to each other; in crosses between induced Tox1– mutants, complications due to the translocation are eliminated and the two loci segregate independently.


1985 ◽  
Vol 27 (4) ◽  
pp. 450-456 ◽  
Author(s):  
M. Taga ◽  
C. R. Bronson ◽  
O. C. Yoder

Crosses involving lab strains of C. heterostrophus that were previously selected for improved fertility yielded high frequencies of four-spored asci and only occasional asci with the full set of eight spores. Fertility in crosses between field isolates was low. Most asci contained two haploid spores; no asci had more than four spores. We investigated the distribution of aborted spores with respect to the three defined genetic loci Mat (mating type), Alb-1 (albinism), and Tox-1 (T-toxin production) and determined the frequency of mitotic twins in four-spored asci. Nonrandom spore abortion was evident from the observations that 80–100% of four-spored asci contained two sets of twins (9% expected for random abortion of mitotic products) and up to 95% of four-spored asci segregated 2:2 for alleles at the Tox-1 locus (67% expected for random abortion of meiotic products), suggesting preferential recovery of nonsister meiotic products. Segregation in crosses between field isolates tended to be skewed in favor of the tox-1a allele (specifies no toxin production). Alleles at Mat and Alb-1 segregated as expected for random abortion of meiotic products in both types of crosses. Low fertility and aberrant segregation among progeny segregating for ability to produce T toxin are likely due in part to abortion-inducing factors linked to Tox-1.Key words: fertility, ascomycetes, T toxin, Helminthosporium maydis, Bipolaris maydis.


2021 ◽  
Vol 9 (6) ◽  
pp. 1128
Author(s):  
Kathleen Cusick ◽  
Gabriel Duran

Saxitoxin (STX) is a secondary metabolite and potent neurotoxin produced by several genera of harmful algal bloom (HAB) marine dinoflagellates. The basis for variability in STX production within natural bloom populations is undefined as both toxic and non-toxic strains (of the same species) have been isolated from the same geographic locations. Pyrodinium bahamense is a STX-producing bioluminescent dinoflagellate that blooms along the east coast of Florida as well as the bioluminescent bays in Puerto Rico (PR), though no toxicity reports exist for PR populations. The core genes in the dinoflagellate STX biosynthetic pathway have been identified, and the sxtA4 gene is essential for toxin production. Using sxtA4 as a molecular proxy for the genetic capacity of STX production, we examined sxtA4+ and sxtA4- genotype frequency at the single cell level in P. bahamense populations from different locations in the Indian River Lagoon (IRL), FL, and Mosquito Bay (MB), a bioluminescent bay in PR. Multiplex PCR was performed on individual cells with Pyrodinium-specific primers targeting the 18S rRNA gene and sxtA4. The results reveal that within discrete natural populations of P. bahamense, both sxtA4+ and sxtA4- genotypes occur, and the sxtA4+ genotype dominates. In the IRL, the frequency of the sxtA4+ genotype ranged from ca. 80–100%. In MB, sxtA4+ genotype frequency ranged from ca 40–66%. To assess the extent of sxtA4 variation within individual cells, sxtA4 amplicons from single cells representative of the different sampling sites were cloned and sequenced. Overall, two variants were consistently obtained, one of which is likely a pseudogene based on alignment with cDNA sequences. These are the first data demonstrating the existence of both genotypes in natural P. bahamense sub-populations, as well as sxtA4 presence in P. bahamense from PR. These results provide insights on underlying genetic factors influencing the potential for toxin variability among natural sub-populations of HAB species and highlight the need to study the genetic diversity within HAB sub-populations at a fine level in order to identify the molecular mechanisms driving HAB evolution.


1993 ◽  
Vol 14 (1) ◽  
pp. 349-354 ◽  
Author(s):  
Francis H. Kirkpatrick ◽  
Maxine M. Dumais ◽  
Hugh W. White ◽  
Kenneth B. Guiseley

2007 ◽  
Vol 173 (3) ◽  
pp. 688-690 ◽  
Author(s):  
Melissa Buzinhani ◽  
Marcos R. Buim ◽  
Maurício Yamaguti ◽  
Rosângela C. Oliveira ◽  
Elena Mettifogo ◽  
...  

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