Atul Kumar Johri
Assistant Professor
School of Life Sciences
Jawaharlal Nehru University
New Delhi -110067, India.
Room No.     :  404
Lab No.         :  409
Off. Phone    :  26704511      
E-mail           :  ajohri@mail.jnu.ac.in

 

Education

MS (1989)
M.Phil (1992)
Ph.D. (1995) University of Delhi, Delhi – 110007, India.

Career:

May, 7-17, 2007 Visiting Scientist, Queensland Institute of Medical research, Brisbane, Australia

June, 2004 –till date

Assist. Professor School of Life Sciences JNU New Delhi India

2002- 2004

Research fellow in Medicine Channing laboratory, Harvard Medical School, Boston MA USA.

2000- 2002

Post Doctoral Associate, Biotechnology and Bioengineering Centre, Tufts University, Medford, MA USA.

2000

Post Doctoral Fellow, Dept. of Chemical Engineering University California, and Riverside, California, USA.

1998-2000

Senior Research Associate, Dept. of Chemistry, University of Delhi, India.

1997

Visiting Scientist, Dept. of Chemical Engineering, University of Waterloo, Waterloo, Ontario, Canada

1995-1997

Senior Research Fellow, Department of Zoology, University of Delhi, India.

Research Projects

Serotyping, invasiveness and Proteomics analysis of Group A Streptococcus. DBT, Govt of India for 2005-2008 (67 Lakhs).

Isolation, Identification and Characterization of Promoter Region of Phosphate Transporter (PiPT) Gene from Root Endophyte Fungus Piriformospora indica . DST, Govt of India 2009-2012.

Development of the transformation system for the Piriformospora indica, CSIR, 2008-2011.

Molecular  epidemiology  of  Group  A  Streptococcus  in  Norh  India:  identification  of  region-specific  vaccine  candidates  Indo-German  ICMR  and  BMBF  Germany  2009-2011 

Awards and Honour

  1. Junior Research Fellowship, Dept. of Environment Government of India. (1993).

  2. Senior Research Fellowship from Council of Scientific and Industrial Research (CSIR) Government of India (1994).

  3. UNESCO-Young Scientist Award in Biotechnology, Paris,France(1997).

  4. Senior Research Associateship from Dept. of Science and Technology, Govt. of India (1998-2000)

  5. Post Doctoral Fellowship at Chemical Engineering, University of California, Riverside, CA USA (2000).

  6. Post Doctoral Assoicatship at Bioengineering Centre, Tufts University, Medford MA USA(2000-2002).

  7. Research Fellowship in Medicine at Channing Laboratory,Harvard Medical School, Boston MA USA (2002).

Membership

New York Academy of Sciences USA

American Society for Microbiology USA.

Selected Publications

  1. Manoj Kumar,  Hemant Kumar, Narendra Tuteja, Meenakshi Dua and Atul Kumar Johri, (2010): Development of electroporation-mediated transformation system for axenically cultivable root endophyte fungus Piriformospora indica. Nature Protocols. http://www.natureprotocols.com/2010/07/22/development_of_electroporation.php 

  2. Vikas Yadav*, Manoj Kumar*, Hemant Kumar, Deepak Kumar Deep, Takshila Tripathi, Ruby Sharma, Narendra Tuteja, Ajay Kumar Saxena and Atul Kumar Johri (2010): A Phosphate Transporter from the Root Endophytic Fungus Piriformospora indica Plays a Role in the Phosphate Transport to the Host Plant. Journal of Biological Chemistry. 285. (*contributed equally).

  3. Kumar M, Yadav V, Tuteja N, Johri AK. (2009) : Antioxidant enzymes activities in maize plants colonized with Piriformospora indica ,  Microbiology. 155:780-790.

  4. Johri AK, Immaculada, M., Broenstrup M., Brettoni, C., Hua, L.,  Gygi, SP, Telford, J., Grandi, G., Paoletti LC. (2007) :Transcriptional and proteomic profiles of Group B Streptococcus type V reveal potential adherence proteins associated with high-level invasion) Infection and Immunity.  Volume 75 (3) 1473-1483

  5. Johri A.K., Paolett, LC, Glaser, P., Dua, M., Sharma, PK, Grandi, G., and Rappuoli, R (2006): Group B Streptococcus” global incidence and vaccine development: Nature Reviews Microbiology 4: (12) 932-942.

  6. Johri A.K., Dua M., Sharma, P., Sharma, A., Saraya, R., Arpana and Hemlata. (2006): Use of Proteomics in Microbial Pathogenesis. Advance BioTech. March. Issue  15-20 (cover and feature story)

  7. Saxena, A., Mozumdar, S., and Johri A.K. (2006) Ultra-low sized cross-linked polyvinylpyrrolidone nanoparticles as non-viral vectors for in vivo gene delivery.  Biomaterials.  27(32):5596-602 

  8. Johri AK, Patwardhan V, Paoletti LC (2005) : Growth rate and oxygen regulates  interaction of group B Streptococcus with polarized epithelial cells Canadian J.  Microbiol.  51: 283-286.

  9. Mikamo H, Johri AK, Paoletti LC, Madoff LC, Onderdonk AB., (2004)   Adherence to, invasion by, and cytokine production in response to serotype VIII group B Streptococci. Infection and Immunity.  72 (8):4716-22.

  10. Johri AK, Padilla J, Malin G, Paoletti LC. (2003)  Oxygen regulates invasiveness and virulence of group B streptococcus. Infection and Immunity. 71(12):6707-11.

  11. Johri A.K. Manssur, Y. and David L. Kaplan. (2003) Incorporation of Fluorinated fatty acids into emulsan by Acinetobacter calcoaceticus RAG-1 Biochemical Engineering Journal 16 (2),  175-181

  12. Johri AK, Blank W, Kaplan DL. (2002) : Bioengineered emulsans from Acinetobacter calcoaceticusRAG-1 transposon mutants. Appl Microbiol Biotechnol.  59(2-3):217-23.

  13. Dua M, Singh A, Sethunathan N, Johri AK. (2002) Biotechnology and bioremediation successes and limitations. Appl Microbiol Biotechnol.  59 (2-3):143-52. 

  14. Panilaitis B, Johri A, Blank W, Kaplan D, Fuhrman J. (2002)    Adjuvant activity of emulsan, a secreted lipopolysaccharide from acinetobacter calcoaceticus. Clin Diagn Lab Immunol. 9 (6):1240

  15. Johri AK, Dua M, Saxena DM, Sethunathan N. (2002) Enhanced degradation of hexachlorocyclohexane isomers by Sphingomonas paucimobilis. Current Microbiology. ; 41(5):309-11.

  16. Johri AK, Dua M, Singh A, Sethunathan N, Legge RL. (1999) Characterization and regulation of catabolic genes. Critical Reviews Microbiology. 25(4):245-73.

  17. Johri AK, Saxena DM, Lal R. (1997)   Interaction of synthetic pyrethroids with micro-organisms a review. Microbios.; 89(360-361):151-156..

  18. Johri AK, Dua M, Tuteja D, Saxena R, Saxena DM, Lal R. (1996) Genetic manipulations of microorganisms for the degradation of hexachlorocyclohexane. FEMS Microbiology Reviews. 19(2):69-84.

  19. Johri, A.K., Dua M. Tuteja, D., Saxena, R., Saxena, D.M., and Lal, R. (1998)  Degradation of Alpha, beta, gamma and delta-hexachlorocylohexanes by Sphingomonas paucimobilis. Biotechnology Letters, 20 (9):885-889.

  20. Johri A.K., Saxena D.M. and Lal R.  (1994) Impact of Synthetic pyrethroid insecticide fenvalerate on Tetrahymena thermophila. Pestic. Res. J. 61994 (1); 60-66.

Chapters

Kuhad A., Johri A K and Singh A (2005) Biodegradation of pesticides (Invited contribution) book on Bioremediation Eds (Singh A and Ward O.P. Elsevier Science Publishers).

Invited talks
  1. Use of proteomics in vaccine development against Group B Streptococcus causing mortality in infants, ISCBC-09, Department of Chemistry, Delhi University, Delhi (2009).

  2. Use of ultra low size nanoparticles for the diagnosis of the microorganisms. PDM college of Pharmacy Bahadurgarh, Haryana, (2009).

  3. Use of Nanotechnology in drug and gene delivery. College of Life Science, Gwalior cancer hospital and research institute, M.P. (2008).

  4. Use of Nanotechnology in detection of cancer (International symposium on cancer, JNU, New Delhi 18-20 December (2008).

  5. Use of nanosystems in microbial pathogenesis. Indo-Australian conference on nanoscience and naotechnology and its applications, Delhi University, Delhi, 19-21 Dec (2007)

  6. Use of ultra-low size nanoparticles for gene targeting. Internatinal conference on nanoscience and nanotechnology, AIT, Gourgoan, Haryana 19-21 Dec, (2007)

  7. Application of Proteomics in Microbial pathogenesis, Queensland Institute of Medical Research , Brisbane, Australia in the laboratory of Prof. Sriprakrash 13 May (2007).

  8. Proteomics and Group B Streptococcus vaccine development. Invited speaker 47 AMI conference Association of Microbiologists of India Bhopal, India (2006)

  9. Use of Proteomics in Group B Streptococcus vaccine development. Pasteur Institute, Genomics microbial pathogenesis unit Paris, France, 13 June (2006).

  10. Role of Proteomics in Microbiology, for Biospark (2005) SLS, JNU, New Delhi, India

  11. Proteomics analysis of group B Streptococcus, Bioinformatics center JNU for a training course. (2005).

  12. Application of Proteomics in Microbial pathogenesis Jamia Milia Islamia, for UGC Academic college course training program (2005).

Regional, National, or International Contributions:

1991

The Second Congress of Asia and Oceania Society of Comparative Endocrinology New Delhi, India.

1993

Effect of synthetic pyrethroid insecticide fenvalerate on Tetrahymena thermophila National symposium on pesticides Future Scenario. Indian Agricultural Research Institute (I.A.R.I.) Pusa, New Delhi, India.

1994

Use of microbes for the degradation of xenobiotics. National symposium on environment II, National Chemical Laboratory (NCL) Invited Speaker Pune, India.

1994

Cloning of catabolic genes responsible for the degradation of gamma – HCH. Micon-International-94 & 35 Annl. Conf. Asso. Microbiol. India. DFRL, Mysore, India.

1996

Kinetics of degradation of alpha, beta, gamma and delta-HCH by Sphingomonsas paucimobilis A laboratory study. Symposium on Biodegradation of organic pollutants, Mallorca, Spain.

1996

Genetic engineering a tool for the degradation of the aromatic hydrocarbons. National symposium on towards green and sustainable environment, Indian Agriculture Research Institute Pusa, New  Delhi, India.

1996

Degradation of HCH isomers by Sphingomonas paucimobilis Molecular Genetics studies. International symposium on subsurface microbilogy (ISSM-96) Davos, Switzerland.

2001

Analysis of biogengineered emulsans from Acinetobacter calcoaceticus RAG-1 and transposon mutants No 18 page 38. Bioengineering meeting Tufts University Science and Technology Centre, Medford MA USA

2001

Engineering of microbial biopolymer analogs. 221 American Chemical Society (ACS) meeting San Diego, California, USA

2002

Effect of Oxygen on Group B Streptococcal Invasiveness. Annual Meeting of Proc Soc., Harvard Medical School, Boston MA USA

2003

Oxygen regulates invasiveness of group B Streptococcus, 103rd general meeting of American Society for Microbiology May  18-22, 2003 Washington DC. USA

2004

Interaction of Group B Streptococcus with Polarized A549 cells American Society for Microbiology May 23-27, 2004l. New Orleans, LA USA

2006

Proteomics and Group B Streptococcus vaccine development 47 Microbiology conference, 6-8 December, Bhopal India (Invited speaker)

2007

Prediction of eligible vaccine candidates of Group A Streptococcus (GAS) by using bioinformatics approach Poster No:P43, Indo-Australian Biotechnology conference, QIMR, Brisbane, Australia, 7-9 May (2007).

2007

Molecular typing and invasiveness of Group A Streptococcus (GAS) of Indian origin, Poster No: P46, Indo-Australian Biotechnology conference, QIMR, Brisbane, Australia, 7-9 May (2007).

2007 Convener: Symposium on Nanotechnology and its applications in biological science, 14 Dec 2007 Jawaharlal Nehru University, New Delhi, India.
2008 Member executive committee International symposium cancer JNU 2008.
2008 Poster, American Society for Microbiology,general meeting, Boston, USA 2008.
2009 Comparative analyses of of Pili Expression by Streptococcus agalactiae Strains of Indian and United States Origin,American Society for Microbiology, Poster , 105general meeting, Philadelphia, USA 2009.

 

Research Specialization:

Microbial Pathogenesis, Genomics, Proteomics and Infectious Disease, Microbial Biotechnology, Bioengineering, Biomedical Engineering, Microbial Degradation of Xenobiotics, Nanotechnology.

(1) Vaccine development for Group A Streptococcus and Group B Streptococcus
We would be using reverse vaccinology approach like Proteomics, Genomics and Bioinformatics for vaccine development for Group B Streptococcus and Group A Streptococcus and other infectious microorganisms using dynamic in vitro attachment and invasion system (DIVAS), a system that combines the advantages of controlling bacterial growth by continuous culture methods with perfusion tissue culture and 60mm dishes. We would be studying invasion and adherence of the group B Streptococcus and other infectious microorganisms with various epithelial and endothelial cell lines to fish out role of various proteins and genes that are upregulated and are involved in invasion and adherence by using SDS-PAGE and 2D-gel electrophoresis, MALDI-TOF-TOF, electro spray ionization liquid chromatography tandem mass spectrometry (ESI-LC-MS/MS), and DNA Micro-array etc.

Figure 1: Streptococcus pyogenes on blood agar plates illustrating β-hemolysis


(2) Use of nanoparticles (non-viral vectors) as gene and drug deliver vectors
In principle, the technique of gene delivery involves taking complete or parts of genes that can code specific message and delivering them to selected cells in the body. Such a transfer of plasmid DNA into mammalian cells has posed major challenges for gene therapy. Although viral vectors are attractive in terms of the scientific strategy of exploiting natural mechanism, such systems suffer from inherent difficulties of effective pharmaceutical processing, immunogenicity, scale up and the possibility of reversion of an engineered virus to the wild type. Non-viral vectors, on the other hand, offer some acute advantages as they can safely transfer larger pieces of DNA, they are weakly immunogenic and are easier to use and produce. Consequently, a major focus is now being given at the development and use of non-viral vectors for safe and efficient delivery of gene. We would be using chitosan, gelatin and emulsan as biomaterials for gene and drug targeting in vitro and in vivo.

Figure 2: Transmission Electron Microscopy picture of PVP nanoparticles encapsulating pDNA. Average size of the nanoparticles is < 100nm. The bar represents 200 nm.

(3) Plant microbe interactions
Arbuscular mycorrhiza (AM) is one of the most prominent symbiotic associations between plant root and fungi. These obligatory biotrophic fungi colonize the root cortex and form arbuscules with in the root cortical cells and also develop a network of hyphae which extend into the soil. Phosphate and carbon transfer between the symbionts is thought to occur at the arbuscule/cortical cell interface. The mechanism by which the plant and symbiont benefit from the association are complex, but it is well documented that the AM fungi absorb mineral nutrients (mainly phosphorus) from the soil and transport them to the host plant, while the fungi acquire photosynthates (reduced carbon) from the plant. The transport of phosphorus by mycorrhizal fungi is particularly significant because phosphorus often becomes depleted around roots due to its high requirement and relative immobility in the soil, thus creating a phosphorus depletion zone. In fungi, the plasma membrane H+-ATPase and phosphate transporter are involved in the phosphorous uptake from the soil, its metabolism and transport to the host plant. We are looking for a phosphate transporter gene and interacting partners in P. indica using cDNA and yeast two hybrid library and PCR techniques.


Figure 3: Visual morphological appearance of fungi P. indica (Axenic growth)

Collaborators:

(1) Dr. L.C. Paoletti: Associate Professor of Medicine, Channing Laboratory, Harvard Medical School, Boston, MA, USA

(2) Dr. Philippe Glaser: Director, Genomics Microbial Pathogenesis unit, Pasteur Institute, Paris, France

(3) Dr. N Tuteja: Associate Scientist, Plant Molecualr Biology , ICGEB, New Delhi, India

(4) Dr. Meenakshi Dua: Assistant Professor, School of Environmental Sciences, JNU, New Delhi

(5) Dr. Rino Rappuoli, Global Head, Novartis Vaccine, Italy

(6) Prof. R. Stroud, and Dr. William Harries, Director, Membrane Biology center, University of California, San Francisco, USA

(7) Prof. G.S. Singh Chhatwal, Head, Helmontz Center for Infectious disease, Germany.

(8) Prof. Geeta Mehta: Head, Microbiology, Lady Hardinge Medical College, Delhi

(9) Dr. Dipti Nayyar, Department of Microbiology, Safdarjung Hospital, New Delhi

Group Members:

Abhinay Sharma: (SRF UGC): Serotyping, invasiveness and proteomics analysis of Group A Streptococcus vaccine development

Hemlata: (SRF CSIR): Group B Streptococcus serotyping, invasivness and transcriptional profiling

Hemant Kumar:  (SRF CSIR) : Expression and purification and structural analysis of a phosphate transporter (PiPT) from axenically grown endophyte fungus P. indica

Deepak Kumar: (SRF RGNF): Group A Streptococcus serotyping and interaction with lung cell line (A549)

Manoj Kumar: Plant microbe interaction using P indica as a model system

Ruby Sharma (Project Fellow, DST)

Takshila Tripathi (Project fellow, CSIR)

Pratap Singh (SRF, CSIR)

Dr. Suriya Mir

Ph.D. Supervised: (3)

Dr. Rajani Malla : Reader, Tribhuvan University, Nepal
Dr. Vikas Yadav : Post Doctoral Fellow, Tufts University, Boston, USA
Dr. Puja Sharma : Post Doctoral Fellow, Harvard Meedical School, Harvard University, Boston, USA.

Ph.D. Registered: 6

M.Phil supervised: 3

MS supervised: 15

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