- Open Access
A novel virus that infecting hypovirulent strain XG36-1 of plant fungal pathogen Sclerotinia sclerotiorum
© Zhang et al; licensee BioMed Central Ltd. 2009
- Received: 26 May 2009
- Accepted: 07 July 2009
- Published: 07 July 2009
Sclerotinia sclerotiorum is a notorious plant fungal pathogen which spreads across the world. Hypovirulence is a phenomenon where the virulence of fungal pathogens is decreased, even lost, due to mycovirus infection. The potential of hypoviruses for biological control of the chestnut blight fungus (Cryphonectria parasitica) has attracted much interest, and has led to discovery of new hypovirulent strains in other fungi.
A hypovirulent strain, strain XG36-1, was isolated from a typical lesion on the stem of rapeseed (Brassica napus) caused by Sclerotinia sclerotiorum. Strain XG36-1 grew on PDA very slowly (average 2.5 ± 0.1 mm/d) with sectoring, and developed abnormal colony morphology with few sclerotia. Unlike health strains (such as wildtype strain XG-13), it was unable to induce lesions on detached leaves of rapeseed. Sclerotia of strain XG36-1 produced apothecia rarely. A sexual progeny test showed that the phenotypes of all 104 sexual progeny were not different from wildtype strain XG-13 which shows normal phenotype of S. sclerotiorum, and protoplast regeneration tests showed that 25.5% of the regenerants of strain XG36-1 were recovered fully. Furthermore, the hypovirulence and its associated traits could be transmitted to XG36-1A34 R , a hygromycin-resistance gene labelled sexual progeny of strain XG36-1, by hyphal anastomosis. Transmission electron microscope (TEM) observation showed that the cytoplasm of strain XG36-1 was destroyed and granulated; the membranes of nuclei and mitochondria were disintegrated; and mitochondrial cristae were cavitated. Viral particles (about 40 nm) in hyphae of strain XG36-1, but not in its sexual progeny and wildtype strain XG-13, could be observed with TEM, and several virus-like particles were uniquely enveloped by single layer membrane in the cells of strain XG36-1. Furthermore, the viral particles could be co-transmitted with the hypovirulence traits through hyphal anastomosis.
Hypovirulence and its associated traits of strain XG36-1 could be mediated by a fungal virus. Currently, we could not know the characteristic of this virus, but it likely represent a new type of mycovirus in S. sclerotiorum, and possibly in fungi.
- Viral Particle
- Colony Morphology
- Plant Fungal Pathogen
- Sclerotinia Sclerotiorum
- Fungal Virus
Rapeseed (Brassica napus) is one of the most important oilseed crops, and offers the potential for biodiesel production to relieve the pressure of the current energy shortage. The area planted with rapeseed in China is currently 7.4 million hectares, and the Chinese government encourages farmers to plant more winter rapeseed during late fall to early summer in central China http://www.gov.cn/gzdt/2008-01/11/content_855731.htm. Sclerotinia sclerotiorum (Lib.) de Bary is an important fungal plant pathogen which damages a wide variety of crops throughout the world . In China, this fungus causes stem rot of rapeseed and is responsible for serious losses every year; in 2008, more than 15–70% of rapeseed plants were killed by this pathogen in Hubei Province. Due to the shortage of disease-resistant cultivars, chemical control is currently the only choice to control stem rot. However, there are problems associated with chemical control of stem rot. Firstly, fungicide control requires treatment during the bloom stage of rapeseed, but this is not practical because the chemical does not arrive at the stems efficiently through heavy canopy. Secondly, fungicide-resistant strains of S. sclerotiorum have been frequently isolated in the field . Non-fungicidal alternatives for the control of stem rot of rapeseed are necessary.
Hypovirulence or hypovirulence is a phenomenon where the virulence of fungal pathogens is decreased, even lost, due to mycovirus infection. Hypovirulence was first reported in the chestnut blight, a destructive disease caused by Cryphonectria parasitica by Grente . The successful control of chestnut blight with hypovirulent strains of C. parasitica represented an alternative approach to biological control fungal diseases other than with mycoparasites and antagonists [4, 5]. The potential of hypovirulence for biological control of plant fungal diseases has attracted much interest, and has lead to discovery of new hypovirulent strains in other fungi. Other mycoviruses causing hypovirulence or hypovirulence of plant fungal pathogens include: mitovirus in C. parasitica , Ophiostoma novo-ulmi , Sclerotinia homoeocarpa [8, 9], Chalara elegans  and Botrytis cinerea ; mycoreoviruses in C. parasitica , and Rosellinia necatrix ; and some unclassified mycoviruses, such as SsDRV in the family Flexiviridae in S. sclerotiorum , DaRV in Diarporthe ambigua , FgV-DK21 in Fusarium graminearum [16, 17] and a 33-nm isometric mycovirus in B. cinerea .
Hypovirulent strains have been reported in S. sclerotiorum, such as isolate 91, strain Ep-1PN and isolate S10 [19–21]; and mycoviruses that associated with hypovirulence of S. sclerotiorum were isolated from strain Ep-1PN [16, 22]. Hypovirulence in S. sclerotiorum is likely common since we often isolate some mild strains, even non-virulence strains, from fields. In this paper, we report on a hypovirulent strain isolated from a typical lesion on stem of rapeseed and called XG36-1 which possibly differs from previously reported hypovirulent strains of S. sclerotiorum.
Strain XG36-1 showed hypovirulence phenotype
Multi-phenotype of protoplast regenerants of strain XG36-1
Normal phenotype of sexual progeny of strain XG36-1
Transmission of hypovirulence phenotype of strain XG36-1
Virus particles observed in strain XG36-1
Viral nucleic tides not extracted from strain XG36-1
All attempts to extract dsRNA were not successful. Double-stranded RNA could not be extracted directly from hyphae of strain XG36-1, but could be extracted from previously reported hypovirulent strain Ep-1PN (positive control). No viral RNA sample could be extracted from the pellets precipitated with ultracentrifugation.
Our experiments showed that strain XG36-1 was a hypovirulent strain of S. sclerotiorum. The protoplast regenerants test suggested that the hypovirulence-associated element (HAE) in cells of strain XG36-1 did not distribute equally, and hypovirulence of regenerants derived from protoplasts that without DAE or with a low concentration of HAE were cured or partially cured. All tested sexual progeny showed the wildtype phenotype of S. sclerotiorum suggesting that chromosomal or DNA changes (nuclear genomic mutations) were not responsible for the hypovirulence of strain XG36-1, and that there is likely some mechanism to eliminate HAE during sexual reproduction. Transmission tests showed that the hypovirulence of strain XG36-1 could be transmitted to wildtype strains efficiently. The hypovirulence and its associated traits of strain XG36-1 is similar to previously reported hypovirulent strain Ep-1PN [14, 20, 23]. Thus, the HAE in strain XG36-1 could be transmissible genetic elements.
In fungi, both fungal plasmids and mycoviruses are transmissible genetic elements, and both mycoviruses, and some fungal plasmids may cause hypovirulence to their hosts . Fungal plasmids are not likely to be HAE of strain XG36-1. Extra-chromosomal DNA segments were not observed with agarose gel electrophoresis analysis of whole DNA samples (data not shown). Meanwhile, viral particles were observed in hyphae of strain XG36-1, but not in its sexual progeny nor in wildtype strain XG-13, and viral particles were always associated the transmission of hypovirulence traits of strain GX36-1. Furthermore, the observed elimination of viruses and hypovirulence during sexual reproduction of strain XG36-1 is in accord with the sexual reproductive behaviour of virus-infected ascomycetous fungal hosts, where the viruses are not transmitted to progeny . Thus, the transmissible DAE in strain XG36-1 is likely to be a mycovirus.
The viral particles in strain XG36-1 is possibly a new type of mycovirus that infecting S. sclerotiorum. The distinct characteristic of the viral particles in strain XG36-1 is that the isometric viral particles are enveloped with a single layer membrane which is possibly derived from its host. Viral particles (double membranes bodies, DMB) have been observed in hypovirulent isolate 275 of S. sclerotiorum , but not in hypovirulent strain Ep-1PN and isolate S10 [14, 27]. Furthermore, the average size of DMBs in isolate 275 was about 70 nm in diameter which was much larger that that of viral particles in strain XG36-1.
This unique envelopment of particles has not been observed in other mycoviruses which may or may not encode coat protein. Viruses infect in all the major groups of fungi kingdom, and RNA viruses in the family Chrysoviridae, Hypoviridae, Narnaviridae (Mitovirus), Partitiviridae and Totiviridae are typical fungal viruses . However, more and more fungal viruses were characterized on molecular level, the plenty diversity of fungal viruses in nature is becoming more and more clear. Viral particles in strain XG36-1 are enveloped uniquely, and could cause severe debilitation of host with low titre, suggest that virus infecting strain XG36-1 is most likely to be a novel mycovirus associated with hypovirulence of plant fungal pathogen.
Our work, here, proved that the hypovirulence and it associated traits of S. sclerotiorum strain XG36-1 could not be transfer to sexual progeny vertically, and the hypovirulence associated element (HAE) is not distributed equally in cells of strain XG36-1. Thus, the hypovirulence of strain XG36-1 is not due to the genome mutation. Hypovirulence and its associated traits could be transferred efficiently to vegetative compatible strain XG36-1A34R, a hygromycin resistance gene labelled sexual progeny of strain XG36-1, through hyphal anastomosis. Thus, the HAE in strain XG36-1 is a mobile element.
The cytoplasm of strain XG36-1 was granulated and not well-distributed, the membranes of nuclei and mitochondria were disintegrated; and mitochondrial cristae were cavitated. Viral particles could be observed in cells of strain XG36-1, but not in wildtype strain XG-13 and sexual progeny XG36-1A34. Viral particles could also be extracted with ultracentrifugation from the hyphae of strain XG36-1. Although the viral nucleic acids were not extracted and identified currently, however, comparing to previously reported hypovirulence or debilitation associated mycoviruses, the virus in strain XG36-1 is unique; it is most likely to be a novel mycovirus associated with hypovirulence of plant fungal pathogen.
Fungal strains, media and culture
S. sclerotiorum strain XG36-1 was isolated from a typical lesion on stem of rapeseed at Xiaogan County, Hubei Province, P R China. Strain XG-13, a healthy wildtype strain, was also isolated from another typical lesion in the same rapeseed field as strain XG36-1. Hypovirulent strain Ep-1PN was originally isolated from diseased eggplant . All strains and their derivatives were grown on PDA (potato dextrose agar, PDA) at 20°C, and stored on PDA slants at 4–6°C.
Comparison of cultural characteristics
Strains XG36-1 and XG-13 were maintained on Petri dishes containing 20 ml PDA, and incubated at 20°C for 3 days. To assess growth rates, 5-mm-diameter agar disks from actively growing colony margins of XG36-1 and XG-13 were transferred onto 9-cm-diam Petri dishes containing 20 ml PDA, and then incubated at 20°C. The diameter of colonies of XG-13 and XG36-1 was measured at 24 hour post inoculation (hpi) and 48 hpi, respectively; the hyphal growth rate of the two strains was calculated as follows: growth rate (cm/d) = (48 hpi diam. - 24 hpi diam.)/2. To compare the biomass between XG36-1 and XG-13 produced on PDA, these two strains were grown out on cellophane membranes on top of PDA (20 ml) at 20°C for 48 h, and then the mycelial mass was rolled from the membrane, placed in an 80°C oven for 10 h, and the dry weights were recorded. To compare the colony morphology, the colonies were grown on 20 ml PDA plates at 20°C for up to 15 days.
Pathogenicity test of XG36-1
Agar disks (5-mm-diam.) from actively-growing colony margins of strain XG36-1 and its derivatives and strain XG-13 were placed on the leaves of rapeseed with the mycelial side facing the leaf surface, and then the inoculated leaves were placed in an incubator at 20°C and 100% relative humility for 60 h. Lesion diameter on each inoculated leaf was measured. There were five replicates for each treatment.
Protoplast preparation and regeneration
To obtain protoplasts of strain XG36-1, mycelial-agar discs (5-mm-diam.) cut from actively growing colony margins of strain XG36-1 were transferred onto cellophane membranes overlaying PDA. After 2 days, the mycelia were collected from cellophane membranes, and then ground with sterilized mortar and pestle to make hyphal fragments. Approximately 1 ml of hyphal fragment mush was transferred into a 250 ml flask containing 80 ml PDB (Potato Dextrose Broth, PDB), and shaken at 150 rpm for up to 20 h at 20°C. The filtrate was collected by passing through two layers of sterilized cheesecloth, and the mycelium was washed twice with 100 ml of potassium chloride (KCl) buffer (0.6 mol/L). The mycelial mass was squeezed to remove liquids, and then re-suspended with digestion buffer which contained 1.5 mg/ml Lysing enzymes from Trichoderma harzianum (Sigma-Aldrich, Inc), and then incubated at 32°C for 3 h. The liquid was filtered through four layers for sterilized cheesecloth and than passed through two layers of sterilized filter paper to remove the debris and undigested hyphal fragments. Protoplasts were collected by centrifugation for 10 min at 4000 rpm. The precipitate was washed twice with 0.6 mol/L KCl solution by re-suspension and centrifugation at 4000 rpm for 5 min. The final precipitate was re-suspended with in 0.6 mol/L KCl solution to give 1–2 × 103 protoplasts/ml for regeneration. One hundred microliter of protoplast suspension was gently mixed with 20 ml regeneration medium (RM: sucrose 0.7 M; yeast extract 0.5 g/L, agar 1.5 g/L, adding KCl to a final concentration 0.6 mol/L before use), and poured into a Petri dish (diam. 90 mm). The plates were incubated at 20–22°C for 3–4 days, and then small colonies were observed on the RM plates and transferred onto fresh PDA plates. These subcultures were considered as protoplast regenerants of strain XG36-1. The cultural characteristics and pathogenicity of regenerants were tested with measures described above.
Sexual reproduction and progeny isolation
To collect sclerotia, strain XG36-1 was allowed to grow on sterilized carrot at 20°C for up to one month. After that, sclerotia were harvested and washed with tap water to remove mycelia and debris, and dried at room temperature for up to two weeks. To induce carpogenic germination of sclerotia, the dry sclerotia were placed at -20°C for up to one month, and then the low-temperature treated sclerotia were surface sterilized with 70% ethanol and sowed onto sterilized wet sand and incubated at 15–17°C for up to two months. A few sclerotia then produced apothecia. To obtain ascospores, mature apothecia were placed into a 50 ml syringe with 10 mL sterile water, and then the syringe was capped with silica gel, and then the piston was pushed and pulled several times to allow apothecia to release ascospores. The ascospores suspension was collected and adjusted to a concentration of ~103 spores/ml. To create mono-ascospore cultures, 200 μl of the spore suspension was spreaded over a thin layer of water agar (10 ml water agar in a 90-mm-diam. plate), and then placed at 20°C for 24 h Under light microscopy, the mycelium formed from a single ascospore was excised, and transferred to fresh PDA plate. The cultural characteristics and pathogenicity of mono-ascospore cultures were assessed with the measures described above.
Transmission of hypovirulence
To test the possible transmission of hypovirulence from strain XG36-1, a non-hypovirulent progeny of strain XG36-1, strain XG36-1A34, was randomly selected for labelling with hygromycin B resistance gene (hph) mediated by Agrobacterium transformation ; and one hph-labelled insert which was similar to strain XG36-1A34, named as strain XG36-1A34R, was chosen for the transmission test. Then strain XG36-1A34R was dual cultured with strain XG36-1 in a PDA plate allowing the two colonies to intermingle according to Jiang et al . Mycelial agar plugs at the colony margin of strain XG36-1A34R were placed onto fresh PDA containing 50 μg/mL hygromycin (where unlabelled strains could not grow), and placed at 20°C for 3 to 4 days. Mycelial plugs were taken from the new colonies and transferred into fresh PDA plate without any hygromycin. The cultural characteristics and pathogenicity of subcultures of XG36-1A34R after contacting strain XG36-1 were tested with measures described above.
Transmission electron microscopy (TEM) observation
Strain XG36-1, strain XG-13, strain 36-1A34R and its subcultures after contacting strain XG36-1 were grown on PDA plates for 2–3 days at 20°C, and the mycelia of each strain were collected for TEM observation (FEI Tecnai G2 20 TWIN transmission electron microscope). The approach for TEM observation followed Boland et al . To extract viral particles, strain XG36-1 was grown out on cellophane membranes on top of PDA for 3 days, and mycelia were harvested for extracting virus-like particles (viral particles) according to Ghabrial and Havens . The viral particles were observed under TEM after negative staining with uranyl-acetate. TEM observation was carried out at Institute of Virology, Chinese Academy of Sciences, Wuhan, P R China.
Extraction and confirmation of dsRNA
Mycelia for dsRNA isolation were grown out on cellophane membranes on top of PDA for 2 to 10 days, respectively. Following harvesting, the mycelium was stored at 80°C before use. The procedure for dsRNA extraction described by Xie et al  was used with minor modifications. The RNA sample was first digested with RNase-free DNaseI, treated with S1 nuclease, and then subjected to electrophoretic analysis on 1% agrose gel.
Each test had three to five replicates, and data from the experiments were analyzed using an analysis of variance (ANOVA) in SAS (SAS Software, NJ). Treatment means were compared with the test of least significant difference (LSD) at the p = 0.05.
This work was financial supported by the Commonweal Specialized Research Fund of China Agriculture (3–21) and Program for New Century Excellent Talents in University (NCET-06-0665). We thank Dr Tom Hsiang of the University of Guelph, Canada for his editorial assistance.
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