M M Parida

Summary

Country: India

Publications

  1. pmc Real-time reverse transcription loop-mediated isothermal amplification for rapid detection of West Nile virus
    Manmohan Parida
    Department of Virology, Institute of Tropical Medicine, Nagasaki University, Nagasaki 852 8523, Japan
    J Clin Microbiol 42:257-63. 2004
  2. pmc Rapid detection and differentiation of dengue virus serotypes by a real-time reverse transcription-loop-mediated isothermal amplification assay
    Manmohan Parida
    Department of Virology, Institute of Tropical Medicine, Nagasaki University, 1 12 4 Sakamoto, Nagasaki 852 8523, Japan
    J Clin Microbiol 43:2895-903. 2005
  3. pmc Development and evaluation of reverse transcription-loop-mediated isothermal amplification assay for rapid and real-time detection of Japanese encephalitis virus
    M M Parida
    Division of Virology, Defence Research and Development Establishment, Gwalior, Madhya Pradesh 474002, India
    J Clin Microbiol 44:4172-8. 2006
  4. pmc Japanese Encephalitis Outbreak, India, 2005
    Manmohan Parida
    Division of Virology, Defence Research and Development Establishment, Gwalior, India
    Emerg Infect Dis 12:1427-30. 2006
  5. pmc Rapid and real-time detection of Chikungunya virus by reverse transcription loop-mediated isothermal amplification assay
    M M Parida
    Division of Virology, Defence Research and Development Establishment, Jhansi Road, Gwalior 474002 M P, India
    J Clin Microbiol 45:351-7. 2007
  6. pmc Yeast expressed recombinant Hemagglutinin protein of novel H1N1 elicits neutralising antibodies in rabbits and mice
    T N Athmaram
    Division of Virology, Defence Research and Development Establishment, Ministry of Defence Govt, of India, Gwalior, MP 474 002, India
    Virol J 8:524. 2011
  7. pmc Molecular epidemiology of novel swine origin influenza virus (S-OIV) from Gwalior, India, 2009
    Shashi Sharma
    Division of Virology, Defence Research and Development Establishment, Gwalior 474002, India
    Virol J 8:280. 2011
  8. pmc Reemergence of dengue virus type-3 (subtype-III) in India: implications for increased incidence of DHF & DSS
    Paban Kumar Dash
    Division of Virology, Defence R and D Establishment, Jhansi Road, Gwalior 474002, MP, India
    Virol J 3:55. 2006
  9. pmc Development and evaluation of one step single tube multiplex RT-PCR for rapid detection and typing of dengue viruses
    Parag Saxena
    Division of Virology, Defence Research and Development Establishment, Jhansi Road, Gwalior 474 002, MP, India
    Virol J 5:20. 2008
  10. pmc Appearance of E1: A226V mutant Chikungunya virus in Coastal Karnataka, India during 2008 outbreak
    S R Santhosh
    Division of Virology, Defence R and D Establishment DRDE, Jhansi Road, Gwalior, MP, PIN 474 002, India
    Virol J 6:172. 2009

Collaborators

Detail Information

Publications41

  1. pmc Real-time reverse transcription loop-mediated isothermal amplification for rapid detection of West Nile virus
    Manmohan Parida
    Department of Virology, Institute of Tropical Medicine, Nagasaki University, Nagasaki 852 8523, Japan
    J Clin Microbiol 42:257-63. 2004
    ..These results indicate that the RT-LAMP assay is extremely rapid, cost-effective, highly sensitive, and specific and has potential usefulness for rapid, comprehensive WN virus surveillance along with virus isolation and/or serology...
  2. pmc Rapid detection and differentiation of dengue virus serotypes by a real-time reverse transcription-loop-mediated isothermal amplification assay
    Manmohan Parida
    Department of Virology, Institute of Tropical Medicine, Nagasaki University, 1 12 4 Sakamoto, Nagasaki 852 8523, Japan
    J Clin Microbiol 43:2895-903. 2005
    ..These findings demonstrate that RT-LAMP assay has the potential clinical application for detection and differentiation of dengue virus serotypes, especially in developing countries...
  3. pmc Development and evaluation of reverse transcription-loop-mediated isothermal amplification assay for rapid and real-time detection of Japanese encephalitis virus
    M M Parida
    Division of Virology, Defence Research and Development Establishment, Gwalior, Madhya Pradesh 474002, India
    J Clin Microbiol 44:4172-8. 2006
    ....
  4. pmc Japanese Encephalitis Outbreak, India, 2005
    Manmohan Parida
    Division of Virology, Defence Research and Development Establishment, Gwalior, India
    Emerg Infect Dis 12:1427-30. 2006
    ..Phylogenetic analysis showed that these isolates belonged to genogroup 3...
  5. pmc Rapid and real-time detection of Chikungunya virus by reverse transcription loop-mediated isothermal amplification assay
    M M Parida
    Division of Virology, Defence Research and Development Establishment, Jhansi Road, Gwalior 474002 M P, India
    J Clin Microbiol 45:351-7. 2007
    ....
  6. pmc Yeast expressed recombinant Hemagglutinin protein of novel H1N1 elicits neutralising antibodies in rabbits and mice
    T N Athmaram
    Division of Virology, Defence Research and Development Establishment, Ministry of Defence Govt, of India, Gwalior, MP 474 002, India
    Virol J 8:524. 2011
    ....
  7. pmc Molecular epidemiology of novel swine origin influenza virus (S-OIV) from Gwalior, India, 2009
    Shashi Sharma
    Division of Virology, Defence Research and Development Establishment, Gwalior 474002, India
    Virol J 8:280. 2011
    ..India also witnessed severe H1N1 pandemic virus epidemic with considerable morbidity and mortality in different parts starting from May 2009...
  8. pmc Reemergence of dengue virus type-3 (subtype-III) in India: implications for increased incidence of DHF & DSS
    Paban Kumar Dash
    Division of Virology, Defence R and D Establishment, Jhansi Road, Gwalior 474002, MP, India
    Virol J 3:55. 2006
    ..We have carried out a detailed investigation of the 2004 outbreak by Serosurveillance, RT-PCR, nested PCR, virus isolation and genotyping. We also report the molecular epidemiological investigation of these outbreaks...
  9. pmc Development and evaluation of one step single tube multiplex RT-PCR for rapid detection and typing of dengue viruses
    Parag Saxena
    Division of Virology, Defence Research and Development Establishment, Jhansi Road, Gwalior 474 002, MP, India
    Virol J 5:20. 2008
    ....
  10. pmc Appearance of E1: A226V mutant Chikungunya virus in Coastal Karnataka, India during 2008 outbreak
    S R Santhosh
    Division of Virology, Defence R and D Establishment DRDE, Jhansi Road, Gwalior, MP, PIN 474 002, India
    Virol J 6:172. 2009
    ..This is the first report regarding the appearance of this mutation in Karnataka state of India. The present study identified the presence and association of A226V mutant virus with Chikungunya outbreak in India during 2008...
  11. doi request reprint Loop mediated isothermal amplification (LAMP): a new generation of innovative gene amplification technique; perspectives in clinical diagnosis of infectious diseases
    Manmohan Parida
    Division of Virology, Defence Research and Development Establishment, Gwalior 474002, MP, India
    Rev Med Virol 18:407-21. 2008
    ....
  12. pmc Development and evaluation of reverse transcription loop-mediated isothermal amplification assay for rapid and real-time detection of the swine-origin influenza A H1N1 virus
    Manmohan Parida
    Division of Virology, Defence Research and Development Establishment, Gwalior, India
    J Mol Diagn 13:100-7. 2011
    ..This suggests that the RTLAMP assay is a valuable tool for rapid, real-time detection and quantification of S-OIV in acute-phase throat swab samples without requiring sophisticated equipment...
  13. ncbi request reprint Rapid and real-time detection technologies for emerging viruses of biomedical importance
    M M Parida
    Department of Virology, Defence R and D Establishment, Gwalior 474 002, India
    J Biosci 33:617-28. 2008
    ..The establishment of these real time molecular assays will certainly facilitate the rapid detection of viruses with high degree of precision and accuracy in future...
  14. ncbi request reprint Development and evaluation of SYBR Green I-based one-step real-time RT-PCR assay for detection and quantification of Chikungunya virus
    S R Santhosh
    Division of Virology, Defence Research and Development Establishment, Jhansi Road, Gwalior 474002, Madhya Pradesh, India
    J Clin Virol 39:188-93. 2007
    ..1 to 10(7)PFU/ml. These findings demonstrated that the reported assay has the potential usefulness for clinical diagnosis due to simultaneous detection and quantification of Chikungunya virus in acute-phase patient serum samples...
  15. doi request reprint East Central South African genotype as the causative agent in reemergence of Chikungunya outbreak in India
    P K Dash
    Division of Virology, Defence R and D Establishment, Gwalior, Madhya Pradesh, India
    Vector Borne Zoonotic Dis 7:519-27. 2007
    ..This study conclusively proved the genotype shift from Asian to ECS African as the major factor in the reemergence of Chikungunya in an unprecedented outbreak in India after a gap of 32 years...
  16. doi request reprint Comparative full genome analysis revealed E1: A226V shift in 2007 Indian Chikungunya virus isolates
    S R Santhosh
    Division of Virology, Defence R and D Establishment, Gwalior, MP, India
    Virus Res 135:36-41. 2008
    ....
  17. doi request reprint Emergence of dengue virus type 4 (genotype I) in India
    P K Dash
    Division of Virology, Defence R and D Establishment, Jhansi Road, Gwalior, MP, India
    Epidemiol Infect 139:857-61. 2011
    ..This is the first report regarding the molecular characterization of Indian isolates of DENV-4, which has the potential to be involved in future outbreaks...
  18. ncbi request reprint Comparison of a dipstick dot-ELISA with commercial assays for anti-dengue virus IgM antibodies
    A V Abhyankar
    Division of Virology, Defense Research and Development Establishment, Gwalior, India
    Viral Immunol 19:630-6. 2006
    ..Although the Panbio kit is widely used in various laboratories in India, the DRDE dipstick dot-ELISA promises to be a useful kit because of its field applicability and comparable sensitivity...
  19. ncbi request reprint Development and evaluation of SYBR Green I-based one-step real-time RT-PCR assay for detection and quantitation of Japanese encephalitis virus
    S R Santhosh
    Division of Virology, Defence Research and Development Establishment, Jhansi Road, Gwalior, Madhya Pradesh 474002, India
    J Virol Methods 143:73-80. 2007
    ..These findings demonstrate the potential clinical application of the reported assay as a sensitive diagnostic test for rapid and real-time detection and quantitation of JEV in acute-phase clinical samples...
  20. ncbi request reprint Evaluation of a dipstick ELISA and a rapid immunochromatographic test for diagnosis of Dengue virus infection
    M M Parida
    Division of Virology, Defence Research and Development Establishment, Gwalior, M P, India
    Acta Virol 45:299-304. 2001
    ..The sensitivity of the Dipstick ELISA with reference to the IC test in detecting IgM and IgG antibodies was 84% and 94%, respectively, and the specificity of the Dipstick ELISA was 98% and 92%, respectively...
  21. doi request reprint Comparative complete genome analysis of dengue virus type 3 circulating in India between 2003 and 2008
    Shashi Sharma
    Division of Virology, Defence R and D Establishment DRDE, Jhansi Road, Gwalior 474002, MP, India
    J Gen Virol 92:1595-600. 2011
    ..This is the first extensive study on complete genome analysis of dengue type 3 viruses in India...
  22. doi request reprint Characterization of Chikungunya virus infection in human neuroblastoma SH-SY5Y cells: role of apoptosis in neuronal cell death
    R Dhanwani
    Division of Virology, Defence Research and Development Establishment, Gwalior, India
    Virus Res 163:563-72. 2012
    ..This study suggested the implication of virus induced apoptosis in disease pathogenesis which may give a fresh insight for CHIKV induced neuronal cell damage and antiviral therapeutics...
  23. ncbi request reprint Serological & virological investigation of an outbreak of dengue fever in Gwalior, India
    M M Parida
    Division of Virology, Defence Research and Development Establishment, Gwalior, India
    Indian J Med Res 116:248-54. 2002
    ..A total of 312 febrile indoor patients suspected to have dengue infection were investigated...
  24. doi request reprint Cellular IMPDH enzyme activity is a potential target for the inhibition of Chikungunya virus replication and virus induced apoptosis in cultured mammalian cells
    M Khan
    Division of Virology, Defence Research and Development Establishment, Jhansi Road, Gwalior 474002, MP, India
    Antiviral Res 89:1-8. 2011
    ..The antiviral activity of MPA against Chikungunya virus is mediated through depletion of GTP pool via inhibition of IMPDH as demonstrated by Immunoblotting and different microscopic analysis...
  25. doi request reprint Chemokine profiling of Japanese encephalitis virus-infected mouse neuroblastoma cells by microarray and real-time RT-PCR: implication in neuropathogenesis
    Nimesh Gupta
    Division of Virology, Defence Research and Development Establishment, Jhansi Road, Gwalior 474002, India
    Virus Res 147:107-12. 2010
    ..Pro- and anti-inflammatory agents targeted against chemokines such as CXCL10 may provide possible therapeutic modalities that can mitigate the morbidity associated with JEV infection of the CNS...
  26. doi request reprint Development and evaluation of a 1-step duplex reverse transcription polymerase chain reaction for differential diagnosis of chikungunya and dengue infection
    Paban Kumar Dash
    Division of Virology, Defence Research and Development Establishment, Gwalior, MP 474 002, India
    Diagn Microbiol Infect Dis 62:52-7. 2008
    ..These findings demonstrate the potential clinical and epidemiologic application of D-RT-PCR for rapid sensitive detection, differentiation, and genotyping of DENV and CHIKV in clinical samples...
  27. doi request reprint Application of real-time RT-PCR in vector surveillance and assessment of replication kinetics of an emerging novel ECSA genotype of Chikungunya virus in Aedes aegypti
    Ankita Agarwal
    Division of Virology, Defence Research and Development Establishment, Jhansi Road, Gwalior 474 002, M P, India
    J Virol Methods 193:419-25. 2013
    ..The implementation of the assay in detecting lower viral load makes it a remarkable tool for surveillance of virus activity in mosquitoes. ..
  28. ncbi request reprint Fusogenic peptide as diagnostic marker for detection of flaviviruses
    Priyabrata Pattnaik
    Virology Division, Defence Research and Development Establishment, Jhansi Road, Gwalior 474 002, MP, India
    J Postgrad Med 52:174-8. 2006
    ....
  29. doi request reprint Development and evaluation of antigen capture ELISA for early clinical diagnosis of chikungunya
    Jyoti Shukla
    Division of Virology Division, Defence Research and Development Establishment, Gwalior 474002, India
    Diagn Microbiol Infect Dis 65:142-9. 2009
    ..This can also be used for rapid screening of large numbers of clinical samples in endemic areas during epidemics...
  30. doi request reprint Assessment of in vitro prophylactic and therapeutic efficacy of chloroquine against Chikungunya virus in vero cells
    Mohsin Khan
    Division of Virology, Defence Research and Development Establishment DRDE, Gwalior, MP, India
    J Med Virol 82:817-24. 2010
    ....
  31. doi request reprint Development of a quantitative competitive reverse transcription polymerase chain reaction (QC-RT-PCR) for detection and quantitation of Chikungunya virus
    Shashi Sharma
    Division of Virology, Defence Research and Development Establishment DRDE, Gwalior, MP, India
    Mol Biotechnol 45:49-55. 2010
    ....
  32. doi request reprint Cloning and expression of domain III of the envelope gene of Japanese encephalitis virus: evaluation for early clinical diagnosis by IgM ELISA
    Jyoti Shukla
    Division of Virology, Defence Research and Development Establishment, Gwalior, India
    J Virol Methods 158:165-70. 2009
    ..The recombinant domain III envelope protein based JEV specific ELISA will be useful for rapid screening of large numbers of clinical samples in endemic areas during outbreaks...
  33. ncbi request reprint Production of IgM specific recombinant dengue multiepitope protein for early diagnosis of dengue infection
    Nagesh K Tripathi
    Division of Virology, Defence Research and Development Establishment, Jhansi Road, Gwalior 474002, India
    Biotechnol Prog 23:488-93. 2007
    ..These results show that the in-house dipstick ELISA using rDME-M protein can be used as a promising kit because of its comparable sensitivity, specificity, field applicability, and low cost...
  34. ncbi request reprint Isolation and characterization of Clostridium botulinum type E from soil of Gwalior, India
    R K Dhaked
    Department of Biotechnology, Defense Research and Development Establishment, Gwalior, MP, India
    J Nat Toxins 11:49-56. 2002
    ..Group specific and serotype specific primers amplified the DNA fragments of 260 bp and 445 bp, respectively, indicating Clostridium botulinum type 'E.'..
  35. ncbi request reprint Involvement of caspase and reactive oxygen species in cyanobacterial toxin anatoxin-a-induced cytotoxicity and apoptosis in rat thymocytes and Vero cells
    P V Lakshmana Rao
    Division of Pharmacology and Toxicology, Defence Research and Development Establishment, Jhansi Road, Gwalior 474002, India
    Arch Toxicol 76:227-35. 2002
    ..The study demonstrates that anatoxin-induced apoptosis is possibly mediated by generation of reactive oxygen species and caspase activation...
  36. ncbi request reprint Production, purification and characterization of recombinant dengue multiepitope protein
    Nagesh K Tripathi
    Division of Virology, Defence Research and Development Establishment, Jhansi Road, Gwalior 474002, India
    Biotechnol Appl Biochem 46:105-13. 2007
    ..These results show that the product has a promising potential to be used for diagnosis of dengue in both laboratory- and field-based detection systems with minimum cost and a high degree of sensitivity and specificity...
  37. doi request reprint Production and characterization of recombinant dengue virus type 4 envelope domain III protein
    Nagesh K Tripathi
    Division of Virology, Defence Research and Development Establishment, Jhansi Road, Gwalior 474002, India
    J Biotechnol 134:278-86. 2008
    ..This production system may also be suitable for the high yield of other recombinant dengue proteins...
  38. doi request reprint Assessment of immunogenic potential of Vero adapted formalin inactivated vaccine derived from novel ECSA genotype of Chikungunya virus
    Mugdha Tiwari
    Defence Research and Development Establishment, Gwalior, M P, India
    Vaccine 27:2513-22. 2009
    ....
  39. ncbi request reprint Inhibitory potential of neem (Azadirachta indica Juss) leaves on dengue virus type-2 replication
    M M Parida
    Division of Virology, Defence Research and Development Establishment, Gwalior 474 002, MP, India
    J Ethnopharmacol 79:273-8. 2002
    ..The pure neem i.e. Azadirachtin did not reveal any inhibition on Dengue virus type-2 replication in both in vitro and in vivo systems...
  40. doi request reprint RNA interference mediated inhibition of Chikungunya virus replication in mammalian cells
    Paban Kumar Dash
    Division of Virology, Defence Research and Development Establishment, Jhansi Road, Gwalior, MP 474 002, India
    Biochem Biophys Res Commun 376:718-22. 2008
    ..This is the first report demonstrating the effectiveness of siRNA against in vitro replication of Chikungunya virus...
  41. pmc Development and evaluation of a novel loop-mediated isothermal amplification method for rapid detection of severe acute respiratory syndrome coronavirus
    Thi Cam Thai Hong
    Department of Virology, Institute of Tropical Medicine, Nagasaki University, Nagasaki 852 8523, Japan
    J Clin Microbiol 42:1956-61. 2004
    ..Thus, the RT-LAMP assay reported here has the advantages of rapid amplification, simple operation, and easy detection and will be useful for rapid and reliable clinical diagnosis of SARS-CoV in developing countries...