Cercospora Apii Research Articles

Insights into the identity and infectivity of the fungi causing Cercospora leaf spots on two ornamental aroids in Brazil

AbstractTwo members of the Araceae broadly cultivated as ornamentals, namely Epipremnum aureum (common name golden pothos or, in Brazil, jiboia) and Zantedeschia aethiopica (common name arum lily or, in Brazil, copo‐de‐leite), were observed bearing Cercospora leaf spots. The former is a very common garden plant, whereas the latter is an important crop for the flower industry. An examination of the fungus associated with the disease on each plant revealed a very similar morphology which suggested that those might be conspecific. A polyphasic taxonomic study, including phylogenetic analyses based on act, cal and his3 sequences, was conducted. Both isolates from the two aroids were found to belong to the Cercospora apii complex, but were genetically distinct. Cercospora sp. Q was identified as the etiological agent of the leaf spots on E. aureum, whereas the fungus on Z. aethiopica was found to belong to Cercospora sp. G. Inoculations confirmed the pathogenicity of both isolates to their original hosts, and cross‐pathogenicity assessments revealed that both isolates were capable of infecting both E. aureum and Z. aethiopica. The limited morphological and pathological distinction between the fungi on these two hosts reflects the continued difficulty in the taxonomic treatment and species delimitation for Cercospora sp. G, Cercospora sp. Q, as well as other provisional code‐based Cercospora spp., and other components of the broad C. apii s. lat. complex. The name Cercospora richardiicola (as C. richardiaecola) was mistakenly used for the fungus on Z. aethiopica in earlier publications and this has been corrected herein.

Complete Genome Sequence Resource for Cercospora apii Causing Leaf Spot of Celery.

Cercospora apii is an important seedborne pathogenic fungus causing severe Cercospora leaf spot of celery worldwide. Here, we first present a complete genome assembly of C. apii QCYBC from celery, based on Illumina paired-end and PacBio long-read sequencing data. The high-quality genome assembly contains 34 scaffolds with a 34.81 Mb genome size, 330 interspersed repeat genes, 114 noncoding RNAs, and 12,631 protein-coding genes. The benchmarking universal single-copy ortholog (BUSCO) analysis indicated that 98.2% of the BUSCOs were complete, whereas 0.3, 0.7, and 1.1% were duplicated, fragmented, and missing, respectively. Based on annotation, 508 carbohydrate-active enzymes, 243 cytochromes P450 enzymes, 1,639 translocators, 1,358 transmembrane proteins, and 1,146 virulence genes were identified. This genome sequence provides a valuable reference for future studies to improve understanding of the C. apii-celery pathosystem. [Formula: see text] Copyright © 2023 The Author(s). This is an open access article distributed under the CC BY-NC-ND 4.0 International license.

First Report of Leaf Spot and Blight on Crown Daisy Caused by Cercospora apii in China.

Crown daisy (Glebionis coronaria L.), also known as chrysanthemum greens, is a popular vegetable in Asia, especially in China. The leaves have been used in folk medicine as a tonic for the liver, blood, intestines and to control anemia and high blood pressure. In November 2020, severe leaf spot and blight was observed with 80% to 95% incidence on crown daisy growing in greenhouses in Fengxian, Shanghai, China(121°22'E, 30°53'N). Irregular rounded spots appeared with a light gray center and water-soaked margins. Round lesions enlarged and merged with age, followed by the development of a necrotic area resulting in the typical "frog-eye" and causing a continuous deterioration of crown daisy. Diseased leaves were washed in running water for 30 min. Small fragments (5 × 5 mm) taken from the margin of lesions were disinfected with 1% NaClO for 3 min, rinsed three times with sterile water, cultured on potato sucrose agar (PSA) augmented with 50 mg streptomycin/liter at 26 oC,and incubated in the dark. Colonies had identical morphology, and TH11290202 was selected and deposited in the plant pathology lab of Shanghai Academy of Agricultural Sciences. Mycelium was initially cottony and white and became appressed to the medium and dark brown with time. Conidia did not form on any media, including PSA, PDA, V8 agar (V8A), maize leaf carbonate agar (MLPCA), pepper leaf carbonate agar (PLPCA), etc. To confirm the identity of the pathogen, genomic DNA was extracted from TH11290202 with the cetyltrimethylammonium ammonium bromide (CTAB) method from the mycelia. Five loci were PCR amplified, namely, the internal transcribed spacer (ITS), translation elongation factor (TEF), calmodulin (cmdA), histone (H3) and actin (ACT), using primers ITS1/ITS4 (White et al. 1990), EF1-728F/EF1-986R (Jaklitsch et al. 2005), CAL-F/CAL-R (O'Donnell et al. 2000), cylh3f/cylh3r (Glass and Donaldson 1995), and ACT-512F/ACT-783R (Carbone and Kohn 1999), respectively. The resulting sequences were deposited in GenBank (MW819910, MW981277, MW981278, ON798723, and MW981279). Analysis of the ITS, TEF, cmdA, H3 and ACT gene sequences of isolate TH11290202 revealed that it was a member of the genus Cercospora, sharing 99.79%, 99.66%, 98.10% 99.74% and 100% sequence similarity with type strain of Cercospora apii CBS 116455. A multilocus phylogenetic analysis was performed using sequences from other closely related taxa obtained from GenBank. Based on morphological and molecular characteristics, TH11290202 was identified as C. apii (Crous and Braun 2003; Groenewald et al. 2006; Milosavljević et al. 2014). To confirm pathogenicity, Koch's postulates were fulfilled on 30 mature plants, which were maintained in a growth chamber (at 26 °C, relative humidity 90%, 12/12 h light/dark). Surface-sterilized leaves were sprayed with a mycelial suspension. Brown lesions were formed 7 days after inoculation on 15 plants, whereas the noninoculated controls remained asymptomatic on the other 15 plants. To our knowledge, this is the first report of C. apii causing leaf spot and blight on G. coronaria in China and will provide useful information for developing effective control strategies.

First Report of Cercospora apii sensu lato 'sp. Q' Leaf Spot on Hop in Brazil.

Hop - Humulus lupulus (Cannabaceae) - is an important and ancient, herbaceous, temperate, perennial crop. It is a vine which, although having other uses, is cultivated predominantly for the brewing industry (Laws 2013). Cultivation of hops in Brazil is relatively new and has increased in the last twenty years. There is only one published record of a fungal disease affecting hop in Brazil - powdery mildew (Fagherazzi et al 2021). In January 2021, leaf spots appeared on all eight hops plants ithe collection maintained in the Infectarium, a disease demonstration garden on the campus of the Universidade Federal de Viçosa (UFV), Viçosa, Minas Gerais, Brazil (https://www.infectario.ufv.br/). Symptoms were small, sub-circular to irregular spots, up to 5 mm, with a whitish to grayish center, surrounded by a dark brown necrotic margin, followed by a narrow yellowish outer margin. Older lesions became larger, grayish-brown, coalesced leading to extensive necrosis and stem dieback. A sample was collected, dried in a plant press, and deposited in the Herbarium of UFV (Acc. No VIC 47534). A dematiaceous fungus was found sporulating in the center of the lesions, when examined with a dissecting microscope. Fungal structures were scraped with a scalpel, mounted in lactoglycerol and observed with a light microscope (Olympus BX51). A pure culture was obtained after conidia were transferred onto PDA plates with a sterile fine-pointed needle. A representative isolate was deposited in the culture collection of the UFV (COAD 3368). The fungus had the following morphology: conidiophores cylindrical, geniculate, proliferating sympodially, 53 to 380 µm × 3 to 6.5 µm, 3 to 15-septate, smooth, with thickened and dark conidial scars, brown; conidia acicular to filiform, 47 to 210 µm × 2.5 to 5 µm, 3 to 17-septate, thin‑walled, smooth, with thickened and dark hila, hyaline. This combination is typical of Cercospora apii sensu lato, as described by Crous and Braun (2003). Genomic DNA was extracted from a 7-day-old culture of COAD 3368 and three loci were PCR amplified, namely: actin (ACT), with 512-F and 783-R primers; calmodulin (CAL), using the primers 228F and 2Rd; and histone H3 gene (HIS3), with the primers CYLH3F and CYLH3R. PCR products were sequenced by Macrogen (Seoul, South Korea) and the resulting sequences were deposited in GenBank (OM677624, OM677625 and OM677626, respectively). A multilocus Bayesian phylogenetic grouped COAD 3368 with Cercospora 'sp. Q' (Groenewald et al. 2013). This is a yet unresolved species complex within C. apii. Six 6‑month‑old healthy hop plants (cv. Cascade) were sprayed with a COAD 3368 conidial suspension (105 conidia/ mL) whereas another group of six plants was sprayed with sterile distilled water, serving as controls. Plants were placed in a dew chamber for 5 days and then transferred to a greenhouse bench, where they were observed daily. Thirty days after inoculation, symptoms similar to those observed in the field had developed on all inoculated plants, whereas control plants remained healthy. The fungus growing on inoculated hops produced typical Cercospora conidiophores and conidia. Upon reisolation, pure cultures with the same morphology of COAD 3368 were obtained. There are no previous records of Cercospora 'sp. Q' on hops worldwide. Fungi in Cercospora 'sp. Q' are known to have a broad host-range. A previous record of Cercospora 'sp. Q' leaf spots was published from its observation on Dioscorea cayennensis in the Infectarium (Torres et al. 2016). Damage to the hop plants was severe and it is possible that Cercospora leaf spot will become an emerging threat to commercial hop plantations in Brazil.

Cercospora apii (early blight: celery)

Cercospora apii (early blight: celery)

Phylogeny of cercosporoid fungi (Mycosphaerellaceae, Mycosphaerellales) from Hawaii and New York reveals novel species within the Cercospora beticola complex

The taxonomy of 44 specimens of cercosporoid fungi from Hawaii and New York, USA, was elucidated through multi-locus phylogenetic analyses of the LSU and ITS regions of the nrDNA as well as partial sequences of the actin, calmodulin, histone H3, and translation elongation factor 1-α genes. Sequences of four additional loci, namely, partial beta-tubulin, glyceraldehyde-3-phosphate dehydrogenase, the second largest subunit of RNA polymerase II, and the cercosporin facilitator protein-encoding gene, were used to resolve evolutionary species boundaries within the Cercospora beticola species complex using concatenated multi-locus phylogenies and the genealogical divergence index (gdi). Four novel Cercospora species, C. americana sp. nov., C. hawaiiensis sp. nov., C. manoa sp. nov., and C. tecta sp. nov. are described. Neocercospora carotae comb. nov. is made for Cercospora apii var. carotae, which is neotypified. Cercospora cf. citrulina and Pseudocercospora ocimi-basilici are reported for the first time in Hawaii. Cercospora beticola, Pluripassalora bougainvilleae, and Pseudocercospora pittospori are confirmed in Hawaii. Strelitziana africana, isolated from leaves of Ipomoea pes-caprae and Bougainvillea sp. affected by Cercospora spp., is reported for the first time in the USA.

Diversity of Endophytic Fungi of Psidium guajava (Myrtaceae) and Their Antagonistic Activity against Two Banana Pathogens

Aims: The present study was carried out to determine the diversity of endophytic fungi that colonize the leaves of Psidium guajava, and to evaluate their antagonistic activity against Fusarium oxysporum f.sp. cubense and Mycosphaerella fijiensis which are the two main phytopathogens of banana plants.
 Place and Duration of Study: The research was carried out at Microbiology Laboratory, Faculty of Sciences, University of Yaoundé I and Microbiology Laboratory, Faculty of Biotechnologies, University of Agronomic Sciences and Veterinary Medicine Bucharest, between April 2018 and February 2020.
 Methodology: Fragments of surface sterilized leaves of Psidium guajava were inoculated on Potato Dextrose Agar supplemented with chloramphenicol. The isolated and purified endophytic fungi were identified based on their macroscopic and microscopic characters using a mycological atlas as guide. The non-sporulating isolates were identified by comparing the ITS regions of their DNA to those of known fungi registered in the GenBank database. The antagonistic activity of the endophytic fungi isolated against Fusarium oxysporum and Mycosphaerella fijiensis was screened using dual culture method.
 Results: A total of 28 endophytic fungal were isolated from the leaves of Psidium guajava corresponding to a colonization frequency of 33.33%. These isolates were identified as: Aspergillus sp., Botryosphaeria sp., Fusarium sp., Neoscytalidium sp., Xylaria sp., Phyllosticta capitalensis, Cercospora apii, Xylaria longipes, Phomopsis sp., Phomopsis asparagi, Aspergillus versicolor, Pallidocercospora thailandica, and Xylaria grammica that belonged to the Deuteromycota and Ascomycota divisions. These endophytic fungi inhibited the growth of Fusarium oxysporum f.sp. cubense and Mycosphaerella fijiensis with the percentage inhibition varying respectively from 23.25% to 73.52% and from 21.36% to 100%. The species Botryosphaeria sp., Phomopsis sp., Phomopsis asparagi, and Xylaria longipes exhibited the greatest activity.
 Conclusion: The leaves of Psidium guajava have a fairly varied diversity of endophytic fungi. These endophytic fungi can serve as potential biological control agents against Panama and Sigatoka diseases of banana and also would produce secondary metabolites with antifungal properties.

New phyllosphere hyphomycetes from the montane fagaceous-bamboo forests of Panama

Foliicolous fungi were collected on living plants of mycologically rarely explored plant families in the montane Quercus-Chusquea forest of western Panama. Five new species of the genera Periconiella, Pseudocercospora, Sporidesmium, and Zasmidium are morphologically described from living leaves of Myrsine coriacea (Primulaceae) and Clusia stenophylla (Clusiaceae). A species of Bomarea (B. caldasii, Alstroemeriaceae) is recorded as host for a cercosporoid fungus (Cercospora apii s.lat.) for the first time.

Cryptic diversity, pathogenicity, and evolutionary species boundaries in Cercospora populations associated with Cercospora leaf spot of Beta vulgaris

The taxonomy and evolutionary species boundaries in a global collection of Cercospora isolates from Beta vulgaris was investigated based on sequences of six loci. Species boundaries were assessed using concatenated multi-locus phylogenies, Generalized Mixed Yule Coalescent (GMYC), Poisson Tree Processes (PTP), and Bayes factor delimitation (BFD) framework. Cercospora beticola was confirmed as the primary cause of Cercospora leaf spot (CLS) on B. vulgaris. Cercospora apii, C. cf. flagellaris, Cercospora sp. G, and C. zebrina were also identified in association with CLS on B. vulgaris. Cercospora apii and C. cf. flagellaris were pathogenic to table beet but Cercospora sp. G and C. zebrina did not cause disease. Genealogical concordance phylogenetic species recognition, GMYC and PTP methods failed to differentiate C. apii and C. beticola as separate species. On the other hand, multi-species coalescent analysis based on BFD supported separation of C. apii and C. beticola into distinct species; and provided evidence of evolutionary independent lineages within C. beticola. Extensive intra- and intergenic recombination, incomplete lineage sorting and dominance of clonal reproduction complicate evolutionary species recognition in the genus Cercospora. The results warrant morphological and phylogenetic studies to disentangle cryptic speciation within C. beticola.

First Record of Cercospora apii sensu lato Causing Leaf Spots on Yellow Guinea Yam in Brazil

First Record of Cercospora apii sensu lato Causing Leaf Spots on Yellow Guinea Yam in Brazil

Mycobiota of the weed Tradescantia fluminensis in its native range in Brazil with particular reference to classical biological control

Tradescantia fluminensis [Commelinaceae] (common name wandering Jew or trad), is a native Brazilian herbaceous plant, which has been introduced to be used as an ornamental in many warm areas of the world. In New Zealand and other countries it has become an aggressive invader of natural ecosystems, causing serious environmental disturbances and threatening biodiversity. Surveys of pathogen and insect natural enemies of T. fluminensis were conducted over several years in Brazil to identify potential candidates for use as classical biological control agents in New Zealand. The surveys found seven pathogenic fungi associated with T. fluminensis and related Tradescantia species: Cercospora apii (leaf spot), Rhizoctonia solani (leaf blight), Sclerotium rolfsii (crown rot) and Uromyces commelinae (rust), and three novel species described in this paper: Ceratobasidium tradescantiae sp. nov. (web blight), Colletotrichum riograndense sp. nov. (anthracnose) and Kordyana brasiliensis sp. nov. (white smut-like disease). Observations of damage in the field and expected host-range suggest that K. brasiliensis and U. commelinae have the highest potential for use as classical biological control agents.

A conserved proline residue in Dothideomycete Avr4 effector proteins is required to trigger a Cf-4-dependent hypersensitive response.

CfAvr4, a chitin-binding effector protein produced by the Dothideomycete tomato pathogen Cladosporium fulvum, protects the cell wall of this fungus against hydrolysis by secreted host chitinases during infection. However, in the presence of the Cf-4 immune receptor of tomato, CfAvr4 triggers a hypersensitive response (HR), which renders the pathogen avirulent. Recently, several orthologues of CfAvr4 have been identified from phylogenetically closely related species of Dothideomycete fungi. Of these, DsAvr4 from Dothistroma septosporum also triggers a Cf-4-dependent HR, but CaAvr4 and CbAvr4 from Cercospora apii and Cercospora beticola, respectively, do not. All, however, bind chitin. To identify the region(s) and specific amino acid residue(s) of CfAvr4 and DsAvr4 required to trigger a Cf-4-dependent HR, chimeric and mutant proteins, in which specific protein regions or single amino acid residues, respectively, were exchanged between CfAvr4 and CaAvr4 or DsAvr4 and CbAvr4, were tested for their ability to trigger an HR in Nicotiana benthamiana plants transgenic for the Cf-4 immune receptor gene. Based on this approach, a single region common to CfAvr4 and DsAvr4 was determined to carry a conserved proline residue necessary for the elicitation of this HR. In support of this result, a Cf-4-dependent HR was triggered by mutant CaAvr4 and CbAvr4 proteins carrying an arginine-to-proline substitution at this position. This study provides the first step in deciphering how Avr4 orthologues from different Dothideomycete fungi trigger a Cf-4-dependent HR.

Cercosporoid fungi of Poland

<p>The paper presents characteristics of cercosporoid fungal species from three genera, <em>Cercospora</em>, <em>Passalora</em>, and <em>Pseudocercospora</em>, occurring in Poland and deposited in Polish herbaria or to be expected due to the occurrence of their host plants in the Polish flora. The physiographic literature, but primarily own collections, as well as those gathered in the national herbaria, were the object of the revision.</p><p>This monograph provides morphological descriptions, lists of hosts and distribution in Poland and worldwide as well as detailed illustrations for 41 species. Dichotomous keys for identification of fungi parasitizing hosts from different plant families were prepared within the individual fungal genera.</p><p>The present study represents a compilation of 115 cercosporoid species, of which 63 are reported from Poland and another 6 were doubtful and excluded. The fungi parasitize 221 taxa of host plants from 131 genera and 47 families, out of which 158 taxa from 94 genera and 29 families have been actually found in Poland. Fourteen species described in this book belong to <em>Cercospora apii</em> s. l. Nine quarantine species are listed, from which only three have been published so far.</p><p>This study will be helpful to mycologists, plant pathologist, and Polish plant protection services for identification purposes of the fungi concerned.</p>

First Report of Cercospora apii, Causal Agent of Cercospora Early Blight of Celery, in Serbia.

Celery (Apium graveolens var. dulce) is a very important vegetable crop intensively cultivated in eastern and southern Serbia. During a field survey in August and September 2012, we observed symptoms similar to those of Cercospora early blight in eastern Serbia, with some of the affected fields showing up to 80% disease severity. The lesions on leaves were amphigenous, subcircular to angular and more or less confluent. Lesions enlarged and merged with age, followed by the development of necrotic area causing a continuous deterioration of the plant. Conidiophores arising from the stromata formed dense fascicles, sometimes appearing solitary, brown at the base, paler toward the apex, simple, straight to slightly curved, and rarely geniculate (dimensions 40 to 90 × 5 to 8 μm). Conidia were solitary, hyaline, at first cylindro-obclavate then acicular to acicular-obclavate, straight to slightly curved, subacute to obtuse at the apex, while truncated and thickened at the base (dimensions 45 to 160 × 4 to 5 μm), 5 to 13 septate. Based on the morphological features, we identified the pathogen as Cercospora apii Fresen. (2). In order to obtain monosporic isolates of the fungus, single conidia were cultivated on potato dextrose agar (PDA). To confirm the pathogenicity of the isolates, 5 mm-diameter mycelial plugs from the PDA plates were placed upside down on the adaxial leaf surface of 2-week-old celery seedlings of cv. Yuta. Control plants were inoculated with a sterile PDA plug. Three leaves per plant were disinfected with 70% ethanol, epidermis was scratched with a sterile needle to promote the infection, and inoculated. A total of 12 plants were inoculated with the mycelial plugs and 12 were used as control plants. Inoculated and control plants were kept in a moist chamber for 48 h and then transferred to a greenhouse at 25 ± 2°C. After 2 weeks, the first necrotic spots appeared on inoculated leaves, similar to the symptoms manifested in the field, while control plants remained symptomless. The pathogen was re-isolated and its identity was verified based on morphological and molecular features. To confirm the pathogen's identity, three isolates (CAC4-1, CAC24, and CAC30) were subjected to molecular identification based on the internal transcribed spacer region (ITS) using the ITS1/ITS4 universal primers (5), a partial calmodulin gene (CAL) using CAL-228F/CAL2Rd primers (1,4), and partial histone H3 gene (H3) using CYLH3F/CYLH3R primers (3). Sequences of the amplified regions were deposited in GenBank under accessions KJ210596 to KJ210604. The BLAST analyses of the ITS sequences revealed 100% identity with several Cercospora species (e.g., C. apii [JX143532], C. beticola [JX143556], and C. zebrina [KC172066]), while sequences of CAL and H3 showed 100% identity solely with sequences of C. apii (JX142794 and JX142548). Based on combined morphological and molecular data, the pathogen infecting celery was identified as C. apii, which to our knowledge represents the first report of the presence of the causal agent of Cercospora early blight disease in Serbia.

Cercosporoid hyphomycetes associated with Tibouchina herbacea (Melastomataceae) in Brazil

A survey of fungal pathogens associated with cane tibouchina, Tibouchina herbacea (Melastomataceae), was conducted in the neotropics, concentrated in south and southeastern Brazil and aimed at finding potential biological control agents for this herbaceous invasive weed for introduction into Hawaii. Numerous fungal species were found, including five cercosporoid fungi. Four new taxa are described and illustrated here: Passalora tibouchinae, Pseudocercospora subsynnematosa, Pseudocercospora tibouchina-herbaceae and Pseudocercospora tibouchinicola. A phylogenetic analysis of the ITS and TEF-1α regions of the three new species of Pseudocercospora was conducted and confirmed their separation as distinct taxa as indicated by morphological and cultural features. Additionally, Cercospora apii is reported for the first time on T. herbacea. Among the species of fungi described in this study, two appear particularly promising for use in a biological control program because they were found to cause severe disease on T. herbacea: Passalora tibouchinae and Pseudocercospora subsynnematosa. Additional tests, including host-specificity screening, will be required in order to confirm this potential.

Morphological and molecular identification of Cercospora apii on celery in Serbia

C. apii is one of the most damaging plant pathogenic fungi of celery. During the 2012, samples of celery with typical symptoms of leaf blight were collected on the territory of Veliko Grdaište and their identification is performed using morphological and molecular methods. The pathogenicity test was conducted on healthy plants and all tested isolates caused typical symptoms after inoculation. Conidiophores arising from the stromata formed dense fascicles or single, straight to slightly curved, brown. Conidia are solitary, hyaline and septate (5-13 septa), cylindrical to obclavate, or straight to slightly curved, obtuse at the apex. Truncated and thickened at the base. Fragments of the expected length for the internal transcribed spacer (ITS1/ITS4), calmodulin (CAL-228F/CAL2Rd) and histone (CYLH3F/ CYLH3R) gene were amplified and the obtained sequences showed 100% identity with the C. apii sequences deposited in GenBank.

A new species and new records of cercosporoid fungi from ornamental plants in Taiwan

A newly described species of Pseudocercospora from Ficus microcarpa differs from other Pseudocercospora species on Ficus spp. (Moraceae) by small fascicles of branched conidiophores hidden in the suprastomatal chamber and by the absence of leaf spots, of stromata and of external hyphae. Newly recorded fungi on other ornamental plants in Taiwan are Cercospora apii s. lat. (C. pistiae) on Pistia stratiotes, C. flagellaris, Passalora bougainvilleae, Pseudocercospora pancratii, Ps. violamaculans, and Ps. wedeliae.

Moringa oleifera, a new host record of Cercospora apii s. lat. from Uttar Pradesh, India

Introduction Moringa oleifera Lam. belongs to family Moringaceae and is commonly called muringa or sahjan. It was introduced from tropical Asia or Malaysia in prehistoric times and is now pan tropic in cultivation, commonly found in India. The flowers and fruits are fried and used as a vegetable. It also has medicinal value as a blood purifier and for treatment of skin diseases, eye diseases, paralysis, antibiotic, scurvy, flatulence, galactagogue, dog bite, antispasmodic, hysteria, vulnerary, diuretic, rubefacient, counterirritant, neuralgia, earache, inflammation, caries, headache, palsy, rheumatism, gout, edema, dyspepsia and lumbago. Due to its great significance in medicine, the plant has high demand but attack by the foliicolous fungus, Cercospora apii s. lat. causes serious foliar infection resulting in the death of leaves. Upon critical morphological examination and comparison of morphological features with closely related fungi, the collection appears as a new host record of Cercospora apii s. lat..

First Report of Cercospora apii Leaf Spot on Capsicum chinense in Brazil.

In Brazil, Capsicum chinense Jacq. is the predominant species of commercial hot peppers because of its popular citrus-like aroma and adaptability to different soils and climates (4). In June 2010, 30 samples of C. chinense with severe leaf spot were collected from a field in the city of Viçosa, state of Minas Gerais, Brazil. Symptoms were observed on leaves, calyxes, fruits, and stems on most of the plants found in the area. On leaves, symptoms included amphigenous lesions that were initially circular to ellipsoid, 1 to 5 mm in diameter, whitish to tan in the center, and surrounded by a dark brown or reddish purple border. Lesions coalesce and turned necrotic with age. A fungus isolated from the lesions matched well with the description of Cercospora apii Fresen. It formed erumpent stromata that were dark brown and spherical to irregular; fascicule conidiophores were clear brown or pale, straight or curved, unbranched, geniculate, 22.5 to 80 × 5 to 7.5 μm, 0 to 3 septate, subtruncate apex; and conidia were solitary, hyaline to subhyaline, filiform, base truncate, tip acute, straight to curved, 12.5 to 140 × 3.5 to 5 μm, and 0 to 11 septate (1,2). A sample was deposited in the herbarium of the Universidade Federal de Viçosa, Minas Gerais, Brazil (VIC 31415). Identity was confirmed by amplifying part of the calmodulin gene with species-specific primers CercoCal-apii and CercoCal-R (3) of fungal DNA from a single-spore culture. In amplification reaction, initial denaturation step was done at 94°C for 5 min, followed by 40 cycles of denaturation at 94°C (30 s), annealing at 56°C (30 s), and elongation at 72°C (30 s). Primers CercoCal-apii and CercoCal-R amplified a single DNA product of 176 bp, and coupled with the morphological characteristics, confirmed the identity of the fungus as Cercospora apii. To check pathogenicity, a 6-mm-diameter plug of the isolate was removed from the expanding edge of a 21-day-old culture grown on potato dextrose agar (PDA) and placed in contact with the adaxial face of the leaves of 8-week-old C. chinense grown in 2-liter plastic pots with soil substrate. Six plants, one per pot, were inoculated with the isolate and six plants were inoculated with the fungus-free PDA plug. Inoculated plants were maintained in a moist chamber for 24 h and then subsequently kept in a greenhouse at 26°C. Leaf spot was observed in all inoculated plants 15 days after inoculation and symptoms were similar to those expressed in the field. The fungus was reisolated from the inoculated plants and matched well with the description of Cercospora apii. All fungus-free PDA inoculated plants remained healthy. Cercospora apii comprises a complex of 281 morphologically indistinguishable species that can infect an extremely wide host range (2). To our knowledge, this pathogen has the potential to cause significant damage to the hot pepper industry of Brazil.

Brazilian mycobiota of the aquatic weed Sagittaria montevidensis

Nine species of fungi on the aquatic weed Sagittaria montevidensis (arrowhead) in southern and southeastern Brazil were collected, identified, described and illustrated in a survey for possible biological control agents against this weed. Seven of them are anamorphic fungi, Alternaria alternata, Botrytis cinerea, Cercospora apii, Cercospora sagittariae, Colletotrichum gloeosporioides, Plectosporium alismatis and Pseudocercospora arthrospora, and two smut fungi, Doassansiopsis deformans and Narasimhania alismatis. All represent new host records or new geographic localities for occurrences of the fungi. Pseudocercospora arthrospora is new to science. It differs from known species of genus Pseudocercospora mainly by its subhyaline and disarticulating conidia and host. This fungus is close to Thedgonia but can be distinguished for this genus by its conidiogenesis. Based on the description and disease symptoms Cylindrocarpon sagittariae, recorded on S. trifolia from Japan, is regarded here as a later synonym of Plectosporium alismatis. Preliminary observations of the fungi in the field and in culture suggest that four of these have potential for use as biocontrol agents against S. montevidensis, namely C. sagittariae, C. gloeosporioides, P. alismatis and P. arthrospora.