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organism_group: Fungi ✕

Method / resourceobservedoriginal resultpositivemeasured

Claim · model-written summary

The optimized enzymatic digestion protocol yielded a high quantity of viable protoplasts of C. camelliae.

Taxon
Colletotrichum camelliaeColletotrichum camelliaee0
Outcome
viable protoplastse1
Value
high quantitye1

Verbatim

e0

“Colletotrichum camelliae is a highly virulent fungal pathogen responsible for anthracnose in tea plants”

✓ located verbatim in the source · abstract, characters 13–116
e1

“The optimized enzymatic digestion protocol yielded a high quantity of viable protoplasts”

✓ located verbatim in the source · abstract, characters 1013–1101

Title

PEG-mediated transformation: a tool for random integration or targeted gene replacement in Colletotrichum camelliae

Fang-Fang Huang; Yu-Huan Xie; Qun Hu; et al. Frontiers in Microbiology 2026. doi:10.3389/fmicb.2026.1814272

Other claims from this paper (2)
Method / resourceobservedoriginal resultmeasured

Claim · model-written summary

The assay distinguished L412F and L412V mutations using diagnostic bands.

Taxon
Botrytis cinereaBotrytis cinereat0
Outcome
detect the nucleotide alterationse0
Value
702 bpe0

Verbatim

e0

“A TETRA-primer amplification refractory mutation system polymerase chain reaction (T-ARMS-PCR) was developed to rapidly detect the nucleotide alterations that lead to L412F and L412V mutations, producing a 702 bp band in all isolates, with additional 470 bp (F) or 252 bp (V) fragments”

✓ located after whitespace/quote normalisation · abstract, characters 510–795
t0

“Botrytis cinerea”

✓ located verbatim in the source · title, characters 14–30

Title

Resistance of Botrytis cinerea to anilinopyrimidine fungicides: A novel ARMS ‐ PCR method for the detection of Bcpos5 mutations and characterization of resistance using CRISPR /Cas9 editing

Georgios Sofianos; Athanasios Petmezas; Anastasios Samaras; et al. Pest Management Science 2026. doi:10.1002/ps.70864

Other claims from this paper (9)
Method / resourceobservedoriginal resultmeasured

Claim · model-written summary

The assay detected G408V with MlyI digestion.

Taxon
Botrytis cinereaBotrytis cinereat0
Outcome
confirm the mutatione0
Value
467 bp + 235 bpe0

Verbatim

e0

“Isolates harboring only the 702 bp band were further digested with MlyI to confirm the mutation leading to the amino acid substitution G408V mutation (467 bp + 235 bp)”

✓ located verbatim in the source · abstract, characters 797–964
t0

“Botrytis cinerea”

✓ located verbatim in the source · title, characters 14–30

Title

Resistance of Botrytis cinerea to anilinopyrimidine fungicides: A novel ARMS ‐ PCR method for the detection of Bcpos5 mutations and characterization of resistance using CRISPR /Cas9 editing

Georgios Sofianos; Athanasios Petmezas; Anastasios Samaras; et al. Pest Management Science 2026. doi:10.1002/ps.70864

Other claims from this paper (9)
Method / resourceobservedoriginal resultmeasured

Claim · model-written summary

Sanger sequencing validated the assay results.

Taxon
Botrytis cinereaBotrytis cinereat0
Outcome
Results were validatede0
Comparator
Sanger sequencinge0

Verbatim

e0

“Results were validated by Sanger sequencing”

✓ located verbatim in the source · abstract, characters 966–1009
t0

“Botrytis cinerea”

✓ located verbatim in the source · title, characters 14–30

Title

Resistance of Botrytis cinerea to anilinopyrimidine fungicides: A novel ARMS ‐ PCR method for the detection of Bcpos5 mutations and characterization of resistance using CRISPR /Cas9 editing

Georgios Sofianos; Athanasios Petmezas; Anastasios Samaras; et al. Pest Management Science 2026. doi:10.1002/ps.70864

Other claims from this paper (9)
Method / resourceobservedoriginal resultbasis n/a

Claim · model-written summary

ITS, TEF1-α and RPB2 sequences were deposited in GenBank.

Taxon
Fusarium coffeibaccaeFusarium coffeibaccaet0
Outcome
sequences were deposited in GenBanke0
Value
PV211189 and PV211190e0
Qualifier
TEF1-α (PQ867811 and PQ867812), and RPB2 (PV261064 and PV261065)e0

Verbatim

e0

“sequences were deposited in GenBank as for ITS (PV211189 and PV211190), TEF1-α (PQ867811 and PQ867812), and RPB2 (PV261064 and PV261065).”

✓ located verbatim in the source · abstract, characters 644–781
t0

“Fusarium coffeibaccae”

✓ located verbatim in the source · title, characters 59–80

Title

First Report of Coffea arabica Fruit Rot Disease Caused by Fusarium coffeibaccae in China

Rui Wang; Yunjin Shi; Jin Xu; et al. Journal of Fungi 2026. doi:10.3390/jof12030191

Other claims from this paper (5)
Method / resourceobservedoriginal resultmeasured

Claim · model-written summary

The standard PCR assay had 91.79% sensitivity for C. theobromae detection.

Taxon
C. theobromaeCeratobasidium theobromaee0
Outcome
sensitivitye0
Value
91.79%e0

Not reportedDirection

Verbatim

e0

“C. theobromae was detected in symptomatic samples using a standard PCR assay, with a sensitivity of 91.79% and a specificity of 95.24%”

✓ located verbatim in the source · abstract, characters 630–764

Title

Genome analysis of Ceratobasidium theobromae and its causal association with cassava witches’ broom disease in the Philippines

Cris Q. Cortaga; Alejandra Gil-Ordóñez; Mónica F. Fronda; et al. Frontiers in Fungal Biology 2026. doi:10.3389/ffunb.2026.1800255

Other claims from this paper (7)
Method / resourceobservedoriginal resultmeasured

Claim · model-written summary

The standard PCR assay had 95.24% specificity for C. theobromae detection.

Taxon
C. theobromaeCeratobasidium theobromaee0
Outcome
specificitye0
Value
95.24%e0

Not reportedDirection

Verbatim

e0

“C. theobromae was detected in symptomatic samples using a standard PCR assay, with a sensitivity of 91.79% and a specificity of 95.24%”

✓ located verbatim in the source · abstract, characters 630–764

Title

Genome analysis of Ceratobasidium theobromae and its causal association with cassava witches’ broom disease in the Philippines

Cris Q. Cortaga; Alejandra Gil-Ordóñez; Mónica F. Fronda; et al. Frontiers in Fungal Biology 2026. doi:10.3389/ffunb.2026.1800255

Other claims from this paper (7)
Method / resourceobservedoriginal resultbasis n/a

Claim · model-written summary

WC-02 sequences were deposited in GenBank for ITS, TUB and RPB2.

Taxon
Epicoccum sorghinumEpicoccum sorghinume1
Material
WC-02e0
Outcome
Sequencese0
Value
PZ185680 (ITS), PZ200895(TUB) and PZ200894(RPB2)e0

Verbatim

e0

“Sequences of isolate WC-02 were deposited in GenBank as PZ185680 (ITS), PZ200895(TUB) and PZ200894(RPB2).”

✓ located verbatim in the source · abstract, characters 1463–1568
e1

“Thus, the fungus was identified as Epicoccum sorghinum based on both morphological and molecular data.”

✓ located verbatim in the source · abstract, characters 2068–2170

Title

First Report of Epicoccum sorghinum Causing Leaf Spot on Cassava in China

Yu Wang; Chunxiao Lei; Luoguo Wuremo; et al. Plant Disease 2026. doi:10.1094/pdis-04-26-0803-pdn

Other claims from this paper (13)
Method / resourceobservedoriginal resultmeasured

Claim · model-written summary

Molecular characterization confirmed the pathogen as S. rolfsii.

Taxon
S. rolfsiiAgroathelia rolfsiie0
Outcome
confirmed the pathogen as S. rolfsiie0
Value
98.8–99.0%e0

Verbatim

e0

“Molecular characterisation confirmed the pathogen as S. rolfsii and antagonists as B. subtilis showing 98.8–99.0% nucleotide identity with reference sequences.”

✓ located verbatim in the source · abstract, characters 420–579
t0

“tomato collar rot”

✓ located verbatim in the source · title, characters 41–58

Title

Integrated management strategies against tomato collar rot (Sclerotium rolfsii): A characterisation to management study

ANBU A; SANJEEVKUMAR K; BALABASKAR P; et al. The Indian Journal of Agricultural Sciences 2026. doi:10.56093/ijas.v96i02.172616

Other claims from this paper (12)
Method / resourceobservedoriginal resultpositivemeasured

Claim · model-written summary

Methods were developed for effective transient gene silencing in both conidial and mycelial cells of P. fijiensis.

Organ / stage
conidial and mycelial cellse0
Interactor
P. fijiensisPseudocercospora fijiensise0pathogen
Outcome
effective transient gene silencinge0

Not reportedComparator

Verbatim

e0

“we developed methods for effective transient gene silencing in both conidial and mycelial cells of P. fijiensis”

✓ located verbatim in the source · abstract, characters 458–569

Title

RNA-mediated gene silencing can reduce azole resistance, growth and pathogenicity in Pseudocercospora fijiensis

Flor Yuranny Canacuán Melo; Yohana Katerine Suárez Anaya; Vicente Emilio Rey Valenzuela; et al. PLoS ONE 2025. doi:10.1371/journal.pone.0325057

Other claims from this paper (4)

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