Genetic Analysis of Pathogenicity and Host-specific Toxin Production of Alternaria alternata Tomato Pathotype by Protoplast Fusion

2001 ◽  
Vol 67 (1) ◽  
pp. 7-14 ◽  
Author(s):  
SALAMIAH ◽  
Yukitaka FUKUMASA-NAKAI ◽  
Hajime AKAMATSU ◽  
Hiroshi OTANI ◽  
Keisuke KOHMOTO ◽  
...  
Keyword(s):  
Genetic Analysis ◽  
Protoplast Fusion ◽  
Alternaria Alternata ◽  
Toxin Production ◽  
Tomato Pathotype

Construction and Genetic Analysis of Hybrid Strains between Apple and Tomato Pathotypes of Alternaria alternata by Protoplast Fusion

2001 ◽  
Vol 67 (2) ◽  
pp. 97-105 ◽  
Author(s):  
SALAMIAH ◽  
Hajime AKAMATSU ◽  
Yukitaka FUKUMASA-NAKAI ◽  
Hiroshi OTANI ◽  
Motoichiro KODAMA
Keyword(s):  
Genetic Analysis ◽  
Protoplast Fusion ◽  
Alternaria Alternata

scholarly journals AAL-Toxin-Deficient Mutants of Alternaria alternata Tomato Pathotype by Restriction Enzyme-Mediated Integration

1997 ◽  
Vol 87 (9) ◽  
pp. 967-972 ◽  
Author(s):  
H. Akamatsu ◽  
Y. Itoh ◽  
M. Kodama ◽  
H. Otani ◽  
K. Kohmoto
Keyword(s):  
Restriction Enzyme ◽  
Alternaria Alternata ◽  
Restriction Enzymes ◽  
Toxin Production ◽  
Molecular Genetic Analysis ◽  
Transformation Frequency ◽  
Fungal Genome ◽  
Plasmid Integration ◽  
Tomato Pathotype ◽  
Aal Toxin

Host-specific toxins are produced by three pathotypes of Alternaria alternata: AM-toxin, which affects apple; AK-toxin, which affects Japanese pear; and AAL-toxin, which affects tomato. Each toxin has a role in pathogenesis. To facilitate molecular genetic analysis of toxin production, isolation of toxin-deficient mutants utilizing ectopic integration of plasmid DNA has been attempted. However, the transformation frequency was low, and integration events in most transformants were complicated. Addition of a restriction enzyme during transformation has been reported to increase transformation frequencies significantly and results in simple plasmid integration events. We have, therefore, optimized this technique, known as restriction enzyme-mediated integration (REMI), for A. alternata pathotypes. Plasmid pAN7-1, conferring resistance to hygromycin B, with no detectable homology to the fungal genome was used as the transforming DNA. Among the three restriction enzymes examined, HindIII was most effective, as it increased transformation frequency two-to 10-fold depending on the pathotype, facilitating generation of several hundred transformants with a 1-day protocol. BamHI and XbaI had no significant effect on transformation frequencies in A. alternata pathotypes. Furthermore, the transforming plasmid tended to integrate as a single copy at single sites in the genome, compared with trials without addition of enzyme. Libraries of plasmid-tagged transformants obtained with and without addition of restriction enzyme were constructed for the tomato pathotype of A. alternata and were screened for toxin production. Three AAL-toxin-deficient mutants were isolated from a library of transformants obtained with addition of enzyme. These mutants did not cause symptoms on susceptible tomato, indicating that the toxin is required for pathogenicity of the fungus. Characterization of the plasmid integration sites and rescue of flanking sequences are in progress.

scholarly journals Studies on variability in Alternaria alternata (Kessler) causing leaf blight of Isabgol (Plantago ovata)

2015 ◽  
Vol 12 (2) ◽  
pp. 63-70 ◽  
Author(s):  
RK Meena ◽  
SS Sharma ◽  
S Singh
Keyword(s):  
Alternaria Alternata ◽  
Mycelial Growth ◽  
Toxin Production ◽  
Plantago Ovata ◽  
Mycelium Growth ◽  
Highly Pathogenic ◽  
Fast Growing ◽  
Conidial Morphology ◽  
Incubation Periods ◽  
Pathogenic Variability

All the five isolates of Alternaria alternata isolated from different agro climate zone of Rajasthan were tested for their variability in terms of cultural, conidial, pathogenic characteristics and toxin production. All the five isolates differed in cultural characters i.e. dark black colored and very fast mycelial growth with smooth margins (90.00 mm), light black with white at centre and fast growing (80.00 mm), dark brown and medium mycelium growth with smooth margins (75.00 mm), black colored, medium flat mycelial growth with smooth margins (68.00 mm) and white with slightly black in colour with slow mycelial growth (65.00 mm) were observed in Aa-1, Aa-2, Aa-3, Aa-4 and Aa-5 respectively. The variability in conidial morphology of five different isolates was simple, septate, pale to dark brown in colour, often geniculate with one conidial scar. In respect of pathogenic variability, showed significant variations in terms of disease intensity and incubation periods. The isolates Aa-1 was highly pathogenic on Isabgol cv. RI-89 under artificial inoculation conditions showing 52.12% disease intensity followed by Aa- 3 ,Aa-2, Aa-4 and Aa-5 isolates. The variability in toxin production was reflected in terms of time taken in inducing wilting symptoms of Isabgol cuttings. Isolate Aa-1 was highly toxic followed by isolates Aa-2, Aa-3, Aa-4 and Aa-5. DOI: http://dx.doi.org/10.3329/sja.v12i2.21918 SAARC J. Agri., 12(2): 63-70 (2014)

scholarly journals Distribution and Characterization of AKT Homologs in the Tangerine Pathotype of Alternaria alternata

2000 ◽  
Vol 90 (7) ◽  
pp. 762-768 ◽  
Author(s):  
A. Masunaka ◽  
A. Tanaka ◽  
T. Tsuge ◽  
T. L. Peever ◽  
L. W. Timmer ◽  
...  
Keyword(s):  
Alternaria Alternata ◽  
Sequence Similarity ◽  
Structural Similarity ◽  
Toxin Production ◽  
Brown Spot ◽  
Japanese Pear ◽  
Black Rot ◽  
Acid Moiety ◽  
High Sequence Similarity ◽  
Rough Lemon

The tangerine pathotype of Alternaria alternata produces a host-selective toxin (HST), known as ACT-toxin, and causes Alternaria brown spot disease of citrus. The structure of ACT-toxin is closely related to AK- and AF-toxins, which are HSTs produced by the Japanese pear and strawberry pathotypes of A. alternata, respectively. AC-, AK-, and AF-toxins are chemically similar and share a 9,10-epoxy-8-hydroxy-9-methyl-decatrienoic acid moiety. Two genes controlling AK-toxin biosynthesis (AKT1 and AKT2) were recently cloned from the Japanese pear pathotype of A. alternata. Portions of these genes were used as heterologous probes in Southern blots, that detected homologs in 13 isolates of A. alternata tangerine pathotype from Minneola tangelo in Florida. Partial sequencing of the homologs in one of these isolates demonstrated high sequence similarity to AKT1 (89.8%) and to AKT2 (90.7%). AKT homologs were not detected in nine isolates of A. alternata from rough lemon, six isolates of nonpathogenic A. alternata, and one isolate of A. citri that causes citrus black rot. The presence of homologs in the Minneola isolates and not in the rough lemon isolates, nonpathogens or black rot isolates, correlates perfectly to pathogenicity on Iyo tangerine and ACT-toxin production. Functionality of the homologs was demonstrated by detection of transcripts using reverse transcription-polymerase chain reaction (RT-PCR) in total RNA of the tangerine pathotype of A. alternata. The high sequence similarity of AKT and AKT homologs in the tangerine patho-type, combined with the structural similarity of AK-toxin and ACT-toxin, may indicate that these homologs are involved in the biosynthesis of the decatrienoic acid moiety of ACT-toxin.

scholarly journals Role of the Host-Selective ACT-Toxin Synthesis Gene ACTTS2 Encoding an Enoyl-Reductase in Pathogenicity of the Tangerine Pathotype of Alternaria alternata

2010 ◽  
Vol 100 (2) ◽  
pp. 120-126 ◽  
Author(s):  
Naoya Ajiro ◽  
Yoko Miyamoto ◽  
Akira Masunaka ◽  
Takashi Tsuge ◽  
Mikihiro Yamamoto ◽  
...  
Keyword(s):  
Alternaria Alternata ◽  
Essential Gene ◽  
Toxin Production ◽  
Brown Spot ◽  
Gene Encoding ◽  
Bac Clone ◽  
Biosynthesis Gene Cluster ◽  
Enoyl Reductase ◽  
Alternaria Brown Spot ◽  
Rapid Amplification

The tangerine pathotype of Alternaria alternata produces host-selective ACT-toxin and causes Alternaria brown spot disease of tangerines and tangerine hybrids. Sequence analysis of a genomic BAC clone identified a previously uncharacterized portion of the ACT-toxin biosynthesis gene cluster (ACTT). A 1,034-bp gene encoding a putative enoyl-reductase was identified by using rapid amplification of cDNA ends and polymerase chain reaction and designated ACTTS2. Genomic Southern blots demonstrated that ACTTS2 is present only in ACT-toxin producers and is carried on a 1.9 Mb conditionally dispensable chromosome by the tangerine pathotype. Targeted gene disruption of ACTTS2 led to a reduction in ACT-toxin production and pathogenicity, and transcriptional knockdown of ACTTS2 using RNA silencing resulted in complete loss of ACT-toxin production and pathogenicity. These results indicate that ACTTS2 is an essential gene for ACT-toxin biosynthesis in the tangerine pathotype of A. alternata and is required for pathogenicity of this fungus.

scholarly journals Nonhost Resistance of Arabidopsis thaliana Against Alternaria alternata Involves both Pre- and Postinvasive Defenses but Is Collapsed by AAL-Toxin in the Absence of LOH2

2013 ◽  
Vol 103 (7) ◽  
pp. 733-740 ◽  
Author(s):  
Mayumi Egusa ◽  
Takuya Miwa ◽  
Hironori Kaminaka ◽  
Yoshitaka Takano ◽  
Motoichiro Kodama
Keyword(s):  
Arabidopsis Thaliana ◽  
Alternaria Alternata ◽  
Defense Mechanisms ◽  
Stem Canker ◽  
Hypersensitive Reaction ◽  
Nonhost Resistance ◽  
Necrotrophic Pathogen ◽  
Toxin Resistance ◽  
Tomato Pathotype ◽  
Aal Toxin

The tomato pathotype of Alternaria alternata causes Alternaria stem canker on tomato depending upon the production of the host-specific AAL-toxin. Host defense mechanisms to A. alternata, however, are largely unknown. Here, we elucidate some of the mechanisms of nonhost resistance to A. alternata using Arabidopsis mutants. Wild-type Arabidopsis showed either no symptoms or a hypersensitive reaction (HR) when inoculated with both strains of AAL-toxin-producing and non-producing A. alternata. Yet, when these Arabidopsis penetration (pen) mutants, pen2 and pen3, were challenged with both strains of A. alternata, fungal penetration was possible. However, further fungal development and conidiation were limited on these pen mutants by postinvasion defense with HR-like cell death. Meanwhile, only AAL-toxin-producing A. alternata could invade lag one homologue (loh)2 mutants, which have a defect in the AAL-toxin resistance gene, subsequently allowing the fungus to complete its life cycle. Thus, the nonhost resistance of Arabidopsis thaliana to A. alternata consists of multilayered defense systems that include pre-invasion resistance via PEN2 and PEN3 and postinvasion resistance. However, our study also indicates that the pathogen is able to completely overcome the multilayered nonhost resistance if the plant is sensitive to the AAL-toxin, which is an effector of the toxin-dependent necrotrophic pathogen A. alternata.

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