Prakriti Sharma
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Prakriti Sharma has a total of 21 co-authors. Here are the top co-authors by number of shared publications:
- Rajeev Kumar Tyagi
Biomedical Parasitology and Translational-immunology Lab, University Centre for Research and Development (UCRD), University Institute of Biotechnology, Chandigarh University, Mohali 140413, India
4 shared publications - Nikunj Tandel
Department of Biotechnology, Veer Narmad South Gujarat University (VNSGU)
3 shared publications - Abhishek Ramachandra Panigrahi
Department of Zoology, School of Biological Sciences, Central University of Punjab, Ghudda, Bathinda 151401, India
1 shared publication - Bhishma Raj Dahal
Agriculture and Forestry University, Chitwan, Nepal
1 shared publication - Dinesh Kumar Prajapati
Department of Biotechnology, IIET, Invertis University, Bareilly 243001, India
1 shared publication - Geetika Verma
Department of Experimental Medicine and Biotechnology, Post Graduate Institute of Medical Education and Research (PGIMER), Chandigarh 160012, India
1 shared publication
Latest Publications
- Open Access
- 1 January 2026
- Published by XMLink in Immune Network
- Vol. 26 (5)
Th17/Treg Paradox in Autoimmune Diseases: Treg Dysfunction, Plasticity, and Metabolic Reprogramming
Negi S, et al. Immune Netw. 2026 Oct;26(5):e44. https://doi.org/10.4110/in.2026.26.e44
- 1 January 2026
- Published by XMLink in Immune Network
- Vol. 26 (5)
Open AccessTh17/Treg Paradox in Autoimmune Diseases: Treg Dysfunction, Plasticity, and Metabolic Reprogramming
Negi S, et al. Immune Netw. 2026 Oct;26(5):e44. https://doi.org/10.4110/in.2026.26.e44
- Open Access
- 19 June 2024
- Published by Elsevier in STAR Protocols
- Vol. 5 (3) , 103141
Protocol for oleuropein-induced autophagy mediating drug tolerance in P. falciparum
- 19 June 2024
- Published by Elsevier in STAR Protocols
- Vol. 5 (3) , 103141
Open AccessProtocol for oleuropein-induced autophagy mediating drug tolerance in P. falciparum
- Open Access
- 1 January 2024
- Published by Wiley in Journal of Toxicology
- Vol. 2024 (1) , 5261994
In Vivo Exposure of Deltamethrin Dysregulates the NFAT Signalling Pathway and Induces Lung Damage
Deltamethrin is an insecticide used to control harmful agricultural insects that otherwise damage crops and to control vector‐borne diseases. Long‐term exposure to deltamethrin results in the inflammation of the lungs. The present study elucidates the molecular mechanism underlying the deltamethrin‐induced lung damage. The lung samples were extracted from the Swiss albino mice following the treatment of low (2.5 mg/kg) and high (5 mg/kg) doses of deltamethrin. The mRNA expression of TCR, IL‐4, and IL‐13 showed upregulation, while the expression of NFAT and FOS was downregulated following a low dose of deltamethrin. Moreover, the expression of TCR was downregulated with the exposure of a high dose of deltamethrin. Furthermore, the immunohistochemistry data confirmed the pattern of protein expression for TCR, FOS, IL‐4, and IL‐13 following a low dose of deltamethrin exposure. However, no change was seen in the TCR, NFAT, FOS, JUN, IL‐4, and IL‐13 immunopositive cells of the high‐dose treatment group. Also, ELISA results showed increased expression of IL‐13 in the BAL fluid of animals exposed to low doses of deltamethrin. Overall, the present study showed that deltamethrin exposure induces lung damage and immune dysregulation via dysregulating the NFAT signalling pathway.
- 1 January 2024
- Published by Wiley in Journal of Toxicology
- Vol. 2024 (1) , 5261994
Open AccessIn Vivo Exposure of Deltamethrin Dysregulates the NFAT Signalling Pathway and Induces Lung Damage
Deltamethrin is an insecticide used to control harmful agricultural insects that otherwise damage crops and to control vector‐borne diseases. Long‐term exposure to deltamethrin results in the inflammation of the lungs. The present study elucidates the molecular mechanism underlying the deltamethrin‐induced lung damage. The lung samples were extracted from the Swiss albino mice following the treatment of low (2.5 mg/kg) and high (5 mg/kg) doses of deltamethrin. The mRNA expression of TCR, IL‐4, and IL‐13 showed upregulation, while the expression of NFAT and FOS was downregulated following a low dose of deltamethrin. Moreover, the expression of TCR was downregulated with the exposure of a high dose of deltamethrin. Furthermore, the immunohistochemistry data confirmed the pattern of protein expression for TCR, FOS, IL‐4, and IL‐13 following a low dose of deltamethrin exposure. However, no change was seen in the TCR, NFAT, FOS, JUN, IL‐4, and IL‐13 immunopositive cells of the high‐dose treatment group. Also, ELISA results showed increased expression of IL‐13 in the BAL fluid of animals exposed to low doses of deltamethrin. Overall, the present study showed that deltamethrin exposure induces lung damage and immune dysregulation via dysregulating the NFAT signalling pathway.
- Open Access
Understanding Mutations in Human SARS-CoV-2 Spike Glycoprotein: A Systematic Review & Meta-Analysis
Genetic variant(s) of concern (VoC) of SARS-CoV-2 have been emerging worldwide due to mutations in the gene encoding spike glycoprotein. We performed comprehensive analyses of spike protein mutations in the significant variant clade of SARS-CoV-2, using the data available on the Nextstrain server. We selected various mutations, namely, A222V, N439K, N501Y, L452R, Y453F, E484K, K417N, T478K, L981F, L212I, N856K, T547K, G496S, and Y369C for this study. These mutations were chosen based on their global entropic score, emergence, spread, transmission, and their location in the spike receptor binding domain (RBD). The relative abundance of these mutations was mapped with global mutation D614G as a reference. Our analyses suggest the rapid emergence of newer global mutations alongside D614G, as reported during the recent waves of COVID-19 in various parts of the world. These mutations could be instrumentally imperative for the transmission, infectivity, virulence, and host immune system’s evasion of SARS-CoV-2. The probable impact of these mutations on vaccine effectiveness, antigenic diversity, antibody interactions, protein stability, RBD flexibility, and accessibility to human cell receptor ACE2 was studied in silico. Overall, the present study can help researchers to design the next generation of vaccines and biotherapeutics to combat COVID-19 infection.
Open AccessUnderstanding Mutations in Human SARS-CoV-2 Spike Glycoprotein: A Systematic Review & Meta-Analysis
Genetic variant(s) of concern (VoC) of SARS-CoV-2 have been emerging worldwide due to mutations in the gene encoding spike glycoprotein. We performed comprehensive analyses of spike protein mutations in the significant variant clade of SARS-CoV-2, using the data available on the Nextstrain server. We selected various mutations, namely, A222V, N439K, N501Y, L452R, Y453F, E484K, K417N, T478K, L981F, L212I, N856K, T547K, G496S, and Y369C for this study. These mutations were chosen based on their global entropic score, emergence, spread, transmission, and their location in the spike receptor binding domain (RBD). The relative abundance of these mutations was mapped with global mutation D614G as a reference. Our analyses suggest the rapid emergence of newer global mutations alongside D614G, as reported during the recent waves of COVID-19 in various parts of the world. These mutations could be instrumentally imperative for the transmission, infectivity, virulence, and host immune system’s evasion of SARS-CoV-2. The probable impact of these mutations on vaccine effectiveness, antigenic diversity, antibody interactions, protein stability, RBD flexibility, and accessibility to human cell receptor ACE2 was studied in silico. Overall, the present study can help researchers to design the next generation of vaccines and biotherapeutics to combat COVID-19 infection.
- Open Access
- 8 February 2023
- Published by IntechOpen
Introductory Chapter: Liposome - A Versatile Tool for Drug Delivery in Nanobiomedicine
Open access peer-reviewed chapter
- 8 February 2023
- Published by IntechOpen
Open AccessIntroductory Chapter: Liposome - A Versatile Tool for Drug Delivery in Nanobiomedicine
Open access peer-reviewed chapter
- Open Access
- 25 June 2020
- Published by Agriculture and Environmental Science Academy in Archives of Agriculture and Environmental Science
- Vol. 5 (2) , 168-173
Life cycle and eco-friendly management of Chinese fruit fly (Bactrocera minax) in sweet orange (Citrus sinesis Osbeck) in Nepal
Sweet orange (Citrus sinensis Osbeck) is a highly profitable fruit crop of Nepal. However, for the past five years, farmers experienced poor productivity partly attributed to the severe infestation of exotic Chinese fruit fly (Bactorcera minax), particularly in Sindhuli and Ramechhap district of Nepal. In this context, we attempted to review on identification, life cycle, and eco-friendly management of Chinese fruit fly. The review is documented based on a field visit and relevant works of literature from Journal articles, books, pamphlets, etc. The Chinese fruit fly has tremendous ability to take a long-range flight, thus, migrated from China to Bhutan and crossing the Indo-Nepal eastern border, finally reached to eastern mid-hills of Nepal. Moderate temperature and low humidity of mid-hills of Nepal are favorable for the exponential growth of the pest. Being sweet orange most preferable commodity, the host range of the fly includes almost all the citrus fruits. The fly has damaged 20-50% of the fruit every year and resulted in a loss of millions of rupees. Therefore various pest management practices can be deployed for sustainable eco-friendly management of the pest. The Chinese fruit fly can be successfully managed by hydrolase protein baits, regular pruning, augmentation of bio-control agents, and using soft systemic insecticides. Various other options for the management of Chinese fruit fly are also discussed with their biological efficacy for the sustainable and eco-friendly management of pests.
- 25 June 2020
- Published by Agriculture and Environmental Science Academy in Archives of Agriculture and Environmental Science
- Vol. 5 (2) , 168-173
Open AccessLife cycle and eco-friendly management of Chinese fruit fly (Bactrocera minax) in sweet orange (Citrus sinesis Osbeck) in Nepal
Sweet orange (Citrus sinensis Osbeck) is a highly profitable fruit crop of Nepal. However, for the past five years, farmers experienced poor productivity partly attributed to the severe infestation of exotic Chinese fruit fly (Bactorcera minax), particularly in Sindhuli and Ramechhap district of Nepal. In this context, we attempted to review on identification, life cycle, and eco-friendly management of Chinese fruit fly. The review is documented based on a field visit and relevant works of literature from Journal articles, books, pamphlets, etc. The Chinese fruit fly has tremendous ability to take a long-range flight, thus, migrated from China to Bhutan and crossing the Indo-Nepal eastern border, finally reached to eastern mid-hills of Nepal. Moderate temperature and low humidity of mid-hills of Nepal are favorable for the exponential growth of the pest. Being sweet orange most preferable commodity, the host range of the fly includes almost all the citrus fruits. The fly has damaged 20-50% of the fruit every year and resulted in a loss of millions of rupees. Therefore various pest management practices can be deployed for sustainable eco-friendly management of the pest. The Chinese fruit fly can be successfully managed by hydrolase protein baits, regular pruning, augmentation of bio-control agents, and using soft systemic insecticides. Various other options for the management of Chinese fruit fly are also discussed with their biological efficacy for the sustainable and eco-friendly management of pests.