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. 2015 May;89(9):5060-71.
doi: 10.1128/JVI.03199-14. Epub 2015 Feb 18.

Transfection of Sclerotinia sclerotiorum with in vitro transcripts of a naturally occurring interspecific recombinant of Sclerotinia sclerotiorum hypovirus 2 significantly reduces virulence of the fungus

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Transfection of Sclerotinia sclerotiorum with in vitro transcripts of a naturally occurring interspecific recombinant of Sclerotinia sclerotiorum hypovirus 2 significantly reduces virulence of the fungus

Shin-Yi Lee Marzano et al. J Virol. 2015 May.

Abstract

A recombinant strain of Sclerotinia sclerotiorum hypovirus 2 (SsHV2) was identified from a North American Sclerotinia sclerotiorum isolate (328) from lettuce (Lactuca sativa L.) by high-throughput sequencing of total RNA. The 5'- and 3'-terminal regions of the genome were determined by rapid amplification of cDNA ends. The assembled nucleotide sequence was up to 92% identical to two recently reported SsHV2 strains but contained a deletion near its 5' terminus of more than 1.2 kb relative to the other SsHV2 strains and an insertion of 524 nucleotides (nt) that was distantly related to Valsa ceratosperma hypovirus 1. This suggests that the new isolate is a heterologous recombinant of SsHV2 with a yet-uncharacterized hypovirus. We named the new strain Sclerotinia sclerotiorum hypovirus 2 Lactuca (SsHV2L) and deposited the sequence in GenBank with accession number KF898354. Sclerotinia sclerotiorum isolate 328 was coinfected with a strain of Sclerotinia sclerotiorum endornavirus 1 and was debilitated compared to cultures of the same isolate that had been cured of virus infection by cycloheximide treatment and hyphal tipping. To determine whether SsHV2L alone could induce hypovirulence in S. sclerotiorum, a full-length cDNA of the 14,538-nt viral genome was cloned. Transcripts corresponding to the viral RNA were synthesized in vitro and transfected into a virus-free isolate of S. sclerotiorum, DK3. Isolate DK3 transfected with SsHV2L was hypovirulent on soybean and lettuce and exhibited delayed maturation of sclerotia relative to virus-free DK3, completing Koch's postulates for the association of hypovirulence with SsHV2L.

Importance: A cosmopolitan fungus, Sclerotinia sclerotiorum infects more than 400 plant species and causes a plant disease known as white mold that produces significant yield losses in major crops annually. Mycoviruses have been used successfully to reduce losses caused by fungal plant pathogens, but definitive relationships between hypovirus infections and hypovirulence in S. sclerotiorum were lacking. By establishing a cause-and-effect relationship between Sclerotinia sclerotiorum hypovirus Lactuca (SsHV2L) infection and the reduction in host virulence, we showed direct evidence that hypoviruses have the potential to reduce the severity of white mold disease. In addition to intraspecific recombination, this study showed that recent interspecific recombination is an important factor shaping viral genomes. The construction of an infectious clone of SsHV2L allows future exploration of the interactions between SsHV2L and S. sclerotiorum, a widespread fungal pathogen of plants.

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Figures

FIG 1
FIG 1
Comparisons of the organizations of three isolates of Sclerotinia sclerotiorum hypovirus 2 (SsHV2), isolates SsHV2L, SsHV2/5472, and SsHV2/sx247, with those of Cryphonectria hypoviruses 1, 2, 3, and 4 (CHV1, -2, -3, and -4). (A) Comparisons of the genome sequences of SsHV2L, SsHV2/5472, and SsHV2/sx247 showing the positions of deletions (dotted lines) and insertion of a sequence distantly related to Valsa ceratosperma hypovirus 1 (VcHV1) in SsHV2L. (B) Plot of the nucleotide sequence identities of SsHV2L with SsHV2/5472 and SsHV2/sx247 created with the Recombination Analysis Tool (35). (C) Genome organizations of CHV1, -2, -3, and -4. The positions of the glucosyl transferase, helicase, peptidase, and RNA-dependent RNA polymerase (RdRp) signature sequences are indicated for each open reading frame (ORF).
FIG 2
FIG 2
Neighbor-joining tree depicting the relationships of the predicted amino acid sequences of the large polyproteins of SsHV2L and other confirmed and proposed members of the Hypoviridae. Large polyprotein amino acid sequences of Cryphonectria hypovirus 1 (CHV1, NP_041091), Cryphonectria hypovirus 2 (CHV2, NP_613266), Cryphonectria hypovirus 3 (CHV3, NP_051710), Cryphonectria hypovirus 4 (CHV4, YP_13851), Fusarium graminearum hypovirus 1 (FgHV1, YP_00901106Pl), Phomopsis longicolla hypovirus1 (PlHV1, YP_009051683), Sclerotinia sclerotiorum hypovirus 1 (SsHV1, YP_004782527), Sclerotinia sclerotiorum hypovirus 2/5472 (SsHV2/5472, AHA56680), Sclerotinia sclerotiorum hypovirus 2L (SsHV2L, KF898354), Sclerotinia sclerotiorum hypovirus 2/sx247 (SsHV2-sx247, YP_008828161), and Valsa ceratosperma hypovirus 1 (VcHV1, YP_005476604) were aligned with MUSCLE, and trees were inferred using MEGA6. Horizontal branch lengths are scaled to the expected underlying number of amino acid substitutions per site. Bootstrap percentages of clades are shown (when approximately >50%) along internal branches of the trees. Topologies of the bootstrap majority-rule consensus trees were identical to those inferred from the nonresampled data sets. The plum pox virus (PPV) polyprotein amino acid sequence was used as an outgroup to root the tree.
FIG 3
FIG 3
Comparison of the growth and virulence of Sclerotinia sclerotiorum isolate 328 infected with SsHV2L and SsEV1 and isolate 328 cured of mycovirus infection. (A) Colony morphology of S. sclerotiorum grown on potato dextrose agar at 22°C for 10 days. (B) Comparison of S. sclerotiorum virulence on detached lettuce leaves inoculated with agar plugs containing the pathogen and incubated at 22°C for 72 h. (C) Box plot comparison of mean lesion diameters (cm) on detached lettuce leaves from one of the two trials measured at 48 h after inoculation with mycelial agar plugs.
FIG 4
FIG 4
Comparison of the growth and virulence of virus-free Sclerotinia sclerotiorum isolate DK3 and isolate DK3 transfected with SsHV2L. (A) Agarose gel of dsRNAs from S. sclerotiorum isolates 328, virus-free DK3, and DK3 transfected with in vitro transcripts from a full-length cDNA clone of SsHV2L (0.8% gel; 3-h running time). All samples were purified by CF-11 cellulose chromatography and treated with DNase I. Sizes of DNA ladder standards (lane M) are indicated in kilobase pairs (kb). (B) Box plot comparisons of mean lesion diameters (cm) at 72 h after inoculation with mycelial agar plugs on detached soybean (30 biological replicates) and lettuce (eight biological replicates) leaves. (C) Comparison of colony morphologies of virus-free S. sclerotiorum isolate DK3 and isolate DK3 transfected with SsHV2L grown on potato dextrose agar for 3, 7, and 17 days at 22°C. (D) Attenuation of S. sclerotiorum virulence by SsHV2L on detached soybean leaves at 48 h after inoculation with mycelial agar plugs at 22°C.
FIG 5
FIG 5
Transmission electron micrographs of thin sections of Sclerotinia sclerotiorum isolates 328 and DK3 showing the degradation of mitochondria (M) and of nuclei (N) and the formation of lipid vesicles (V) associated with mycovirus infection. Cross sections through mycelia of virus-free S. sclerotiorum isolate DK3 (A), isolate DK3 transfected with SsHV2L showing vesicles associated with cell walls (B), and isolate 328 infected with SsHV2L and SsEV1 (C) and a high-magnification image of isolate 328 infected with SsHV2L and SsEV1 showing vesicles associated with the nucleus and cytoplasm (D).
FIG 6
FIG 6
Secondary structure model for the 5′ untranslated region (nt 1 to 428) of the Sclerotinia sclerotiorum hypovirus 2L (SsHV2L) genome. Nucleotides are highlighted according to their SHAPE reactivity: black letters, low reactivity; gray letters, medium reactivity; white-filled letters, strong reactivity. The position of the putative 5′ recombination breakpoint in SsHV2L with a virus distantly related to Valsa ceratosperma hypovirus 1 is indicated in the large stem-loop structure beginning at nt 265.

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