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4 results on '"M. Senthil Alias Sankar"'

1. List of contributors

Author

Samuel Abebrese, Noemi Lizbeth Acuña-Flores, Mustafa Adhab, Joseph Adjebeng-Danquah, Parinita Agarwal, Pradeep K. Agarwal, Richard Yaw Agyare, Nawres A. Alkuwaiti, Benjamin Annor, Leonardo D. Arévalo-Monterrubio, José Trinidad Ascencio-Ibáñez, Alexandre Autechaud, Bhagirath M. Baraiya, Natalia Barboza, Mritunjoy Barman, Kwabena Asare Bediako, Eduardo R. Bejarano, Zineb Belabess, Sachin Ashok Bhor, Araceli G. Castillo, Supriya Chakraborty, Swati Chakraborty, Chinnaraja Chinnadurai, Aparna Chodon, Tathagata Choudhuri, Henryk Czosnek, Sarbani Das, Samantha de Jesus Rivero-Montejo, Ragunathan Devendran, Subham Dutta, Vincent N. Fondong, Elizabeth P.B. Fontes, Murad Ghanim, Prabu Gnanasekaran, Alireza Golnaraghi, Gokul Uttamgir Gosavi, Martine Granier, Ramón Gerardo Guevara-González, Vipin Hallan, Luko Hilje, Shridhar Hiremath, Yasir Iftikhar, Shaikhul Islam, Margaux Jammes, Jayaraj Jayaraman, Ajeet Kumar Jha, Jeyalakshmi Karanthamalai, Jawaid A. Khan, Zainul A. Khan, Mounika Kollam, Nagendran Krishnan, Aditya Kulshreshtha, Abhinav Kumar, Alok Kumar, Manish Kumar, R. Vinoth Kumar, Rakesh Kumar, Sailendra Kumar, Shweta Kumari, C.N. Lakshminarayana Reddy, Rosa Lozano-Durán, Israel Macias-Bobadilla, Lalit Mahatma, T. Makeshkumar, V.G. Malathi, Aakansha Manav, Anirban Mandal, Mahsa Mansourpour, M. Mantesh, Humberto Martínez-Montoya, Yamila Martínez-Zubiaur, Laura Mejía-Teniente, Leander Dede Melomey, Ritesh Mishra, M. Mohanraj, Prashant More, Mustansar Mubeen, Arindam Mukherjee, S. Nakkeeran, Michael Kwabena Osei, Koshlendra Kumar Pandey, Gopal Pandi, Harshalkumar P. Patel, Michel Peterschmitt, Malyaj R. Prajapati, Ved Prakash, null Priyanka, Nguyen Bao Quoc, Gabriel S. Raimundo, S.K. Raj, Adesh Ramsubhag, Koushlesh Ranjan, P. Renukadevi, Kumari Rhaeva, Luisa Katiana Rivas-Ramirez, Poonam Roshan, Nabanita Roy Chattopadhyay, Faustine Ryckebusch, Snigdha Samanta, B. Sangeetha, V.K. Satya, Nicolas Sauvion, Sangeeta Saxena, M. Senthil Alias Sankar, Niayesh Shahmohammadi, K.S. Shankarappa, Fredy Davi A. Silva, Jitender Singh, Sneha Sinha, Sunil Kumar Snehi, Ashish Srivastava, Sukumaran Sunitha, Jayanta Tarafdar, Jebasingh Tennyson, Ajay Kumar Tiwari, Reyna Ivonne Torres-Acosta, Rodolfo Torres-delosSantos, Irineo Torres-Pacheco, Eric Troadec, Muhammad Umer, Cica Urbino, Marcela Vargas-Hernandez, V. Venkataravanappa, Heshani De Silva Weligodage, Mengshi Wu, Sneha Yogindran, and Muhammad Ahmad Zeshan

Published
2022
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3. Polymerase chain reaction assay for rapid, sensitive detection, and identification of Colletotrichum gloeosporioides causing greater yam anthracnose

Author

Pravi Vidyadharan, S. Vishnu Nath, M. Senthil alias Sankar, P. V. Archana, M. L. Jeeva, Mithun Raj, and Vivek Hegde

Subjects
Bioengineering, Biology, Applied Microbiology and Biotechnology, Biochemistry, Glomerella cingulata, Polymerase Chain Reaction, Conidium, law.invention, Microbiology, Species Specificity, law, Colletotrichum, DNA, Fungal, Molecular Biology, Pathogen, Polymerase chain reaction, Soil Microbiology, DNA Primers, Plant Diseases, Dioscorea, Fungal genetics, Sequence Analysis, DNA, Spores, Fungal, biology.organism_classification, Spore, Horticulture, Soil microbiology, Nested polymerase chain reaction, Biotechnology
Abstract

Anthracnose caused by Colletotrichum gloeosporioides is an economically important disease which affects greater yam (Dioscorea alata L.) worldwide. Apart from airborne conidia, the pathogen propagules surviving in soil and planting material are the major sources of inoculum. A nested PCR assay has been developed for specific detection of C. gloeosporioides in soil and planting material. In conventional (single-round) PCR, the limit of detection was 20 pg, whereas in nested PCR the detection limit increased to 0.2 pg of DNA. The primers designed were found to be highly specific and could be used for accurate identification of the pathogen up to species level. The protocol was standardized for detection of the pathogen in artificially and naturally infected field samples.

Published
2012

4. Polymerase chain reaction assay for rapid, sensitive detection, and identification of Colletotrichum gloeosporioides causing greater yam anthracnose.

Author

Raj M, Jeeva M, Hegde V, Vidyadharan P, Archana P, Senthil alias Sankar M, and Nath SV

Subjects
Colletotrichum pathogenicity, DNA Primers genetics, DNA, Fungal genetics, Sequence Analysis, DNA, Soil Microbiology, Species Specificity, Spores, Fungal genetics, Spores, Fungal isolation & purification, Colletotrichum genetics, Colletotrichum isolation & purification, Dioscorea microbiology, Plant Diseases microbiology, Polymerase Chain Reaction methods
Abstract

Anthracnose caused by Colletotrichum gloeosporioides is an economically important disease which affects greater yam (Dioscorea alata L.) worldwide. Apart from airborne conidia, the pathogen propagules surviving in soil and planting material are the major sources of inoculum. A nested PCR assay has been developed for specific detection of C. gloeosporioides in soil and planting material. In conventional (single-round) PCR, the limit of detection was 20 pg, whereas in nested PCR the detection limit increased to 0.2 pg of DNA. The primers designed were found to be highly specific and could be used for accurate identification of the pathogen up to species level. The protocol was standardized for detection of the pathogen in artificially and naturally infected field samples.

Published
2012
Full Text
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