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ArticleCurrent microbiology2026

Morpho-Molecular Characterization and Technique for Induction of Growth, Sporulation in Cercospora longipes Causing Brown Spot Disease in Sugarcane.

Dnyaneshwar Borase, Yogesh Thorat, Santosh Watpade, Dinesh Singh, Sayanti Guha Majumdar, Dinesh Singh, R Viswanathan, Jyotsana Tilgam, Prashant Patil, Bharat Bhalerao

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Article in Current microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

10 authors.

Dnyaneshwar BoraseICAR-Indian Sugarcane Research Institute, Biological Control Center, Pravaranagar, Maharashtra, 413712, India. borseiipr@gmail.com.
Yogesh ThoratICAR-Indian Sugarcane Research Institute, Biological Control Center, Pravaranagar, Maharashtra, 413712, India.
Santosh WatpadeICAR-IARI Regional Station, Shimla, Himachal Pradesh, 171004, India.
Dinesh SinghICAR-Indian Sugarcane Research Institute, Lucknow, Uttar Pradesh, 226002, India.
Sayanti Guha MajumdarICAR-Indian Sugarcane Research Institute, Lucknow, Uttar Pradesh, 226002, India.
Dinesh SinghICAR-Indian Sugarcane Research Institute, Lucknow, Uttar Pradesh, 226002, India.
R ViswanathanICAR-Indian Sugarcane Research Institute, Lucknow, Uttar Pradesh, 226002, India.
Jyotsana TilgamICAR-National Bureau of Agriculturally Important Microorganisms (NBAIM), Mau, Uttar Pradesh, 275103, India.
Prashant PatilDepartment of Agricultural Botany, Goa College of Agriculture, Old Goa, Goa, 403402, India.
Bharat BhaleraoMahatma Phule Krishi Vidyapeeth, Rahuri, Maharashtra, 413722, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A significant outbreak of brown spot disease caused by Cercospora longipes E. J. Butler has recently been observed in sugarcane growing regions of India. Cercosporoid fungi grow slowly and sporulate sparsely, making their isolation challenging. In vitro studies were conducted to standardize the isolation technique and optimize the media and culture conditions for growth and sporulation. The causal organism was isolated from brown spot-infected leaves. After 14 days of incubation on PDA, the mycelium exhibited a light yellow-green coloration with dark brown-greenish-black pigmentation. The phylogenetic analysis of ITS region, 18S rRNA, actin, and β-tubulin genes, revealed that Cercospora IISRBCCBP01 isolate form distinct branch, from closely related C. nicotianae, C. kikuchi and C. armoraciae. The morphological characteristics also support this finding, and thus, it was identified as Cercospora longipes. Pathogenicity tests were conducted based on Koch's postulates. Among the fourteen-host plant extract agar media tested, highest growth and conidial production was observed on 25% fresh leaf (FL) + 20% V8 agar media, at a temperature of 25 ℃ and a slightly acidic pH. Continuous light or dark photoperiods induced higher sporulation and growth than alternating light periods. These findings provide a reliable method for isolation and cultivation of this pathogen, while also offering foundational molecular data for future investigations.

Indexed as

CercosporaPlant DiseasesSaccharumSpores, FungalActinsCulture MediaDNA, FungalIndiaPhylogenyPlant LeavesRNA, Ribosomal, 18STubulinActinsCulture MediaDNA, FungalRNA, Ribosomal, 18STubulin

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.