Expression Profiling of Transglutaminase 2 and Inflammatory Host Response in Aspergillus Fumigatus After Treatment with Curcuma Extracts

Authors

  • Omar Sadik Shalal College of health and Medical Technology, Middle Technical University, Baghdad, Iraq

DOI:

https://doi.org/10.51173/jt.v3i4.385

Keywords:

Aspergillus fumigatus, Transglutaminase 2, ROS, Interleukins

Abstract

Aspergillus fumigatus, is considered the most common human pathogen causing Aspergillosis, and is a tough opportunistic pathogen. This pathogen is very capable of forming biofilms via developing hyphal walls radially. The current therapies are known for their limitations where they couldn’t target the proteins involved in undoing host response. Here we aimed to screen the possible antifungal role of Curcumin and its effect on the Transglutaminase 2 and Reactive Oxygen species response. We also screened the levels of cytokines with and without the treatment to confirm the activity. We could neutralize the elevated levels of TG2 by using the treatment (methanol extract). Even the cytokine levels could be normalized with the extract treatment which is usually highly elevated with the fungal infection. We found that TG2 and IL 1β and IL 18 got elevated significantly in control in addition, as well as our extract could confirm the possible role of ROS and its effect on TG2 which is said to play a major role in apoptosis.

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References

akoma, D.O., Department of Biological Sciences (Microbiology Option) Faculty of Science Benson Idahosa University Benin City. 2017.

Hassan, A.S., et al., In-vitro assessment of first-line antifungal drugs against Aspergillus spp. caused human keratomycoses. Journal of Infection and Public Health, 2020. 13(12): p. 1907-1911.

Desforges, M., et al., Human coronaviruses and other respiratory viruses: underestimated opportunistic pathogens of the central nervous system? Viruses, 2020. 12(1): p. 14.

Viegas, C., et al., Aspergillus spp. and azole-resistance characterization on filtering respiratory protective devices from waste sorting industry. 2020.

Ikwegbue, P.C., et al., Interplay between heat shock proteins, inflammation and cancer: a potential cancer therapeutic target. American journal of cancer research, 2019. 9(2): p. 242.

Arias, M., et al., Preparations for invasion: modulation of host lung immunity during pulmonary aspergillosis by gliotoxin and other fungal secondary metabolites. Frontiers in immunology, 2018. 9: p. 2549.

Kolahi, M., et al., Oxidative stress induced by cadmium in lettuce (Lactuca sativa Linn.): Oxidative stress indicators and prediction of their genes. Plant Physiology and Biochemistry, 2020. 146: p. 71-89.

Katt, W.P., M.A. Antonyak, and R.A. Cerione, Opening up about tissue transglutaminase: when conformation matters more than enzymatic activity. Med one, 2018. 3(6).

Dewidar, B., C. Meyer, and S. Dooley, TGF-β in hepatic stellate cell activation and liver fibrogenesis—updated 2019. Cells, 2019. 8(11): p. 1419.

Verzella, D., et al., Life, death, and autophagy in cancer: NF-κB turns up everywhere. Cell death & disease, 2020. 11(3): p. 1-14.

Bhat, A.A., et al., Tight junction proteins and signaling pathways in cancer and inflammation: a functional crosstalk. Frontiers in Physiology, 2019. 9: p. 1942.

Wang, S.-T., et al., Tea polyphenols and their chemopreventive and therapeutic effects on colorectal cancer. World journal of gastroenterology, 2020. 26(6): p. 562.

Lawani-Luwaji, E.U., Differential expression of long and short isoforms of tissue transglutaminase 2; Implications for cisplatin resistance in an in-vitro MCF-7 breast cancer model. 2019, Anglia Ruskin University.

Wouters, A., et al., The intriguing interplay between therapies targeting the epidermal growth factor receptor, the hypoxic microenvironment and hypoxia-inducible factors. Current pharmaceutical design, 2013. 19(5): p. 907-917.

Gundemir, S., et al., Transglutaminase 2: a molecular Swiss army knife. Biochimica et Biophysica Acta (BBA)-Molecular Cell Research, 2012. 1823(2): p. 406-419.

Labib, P.L., G. Goodchild, and S.P. Pereira, Molecular pathogenesis of cholangiocarcinoma. BMC cancer, 2019. 19(1): p. 1-16.

Sieniawska, E., et al., Plant-based food products for antimycobacterial therapy. EFood, 2020. 1(3): p. 199-216.

Süntar, I., et al., Pharmacological and chemical features of Nepeta L. genus: Its importance as a therapeutic agent. Phytotherapy Research, 2018. 32(2): p. 185-198.

Naghdibadi, H., et al., An overview on two valuable natural and bioactive compounds, thymol and carvacrol, in medicinal plants. Journal of Medicinal Plants, 2017. 16(63): p. 1-32.

Salehi, M., M.R. Naghavi, and M. Bahmankar, A review of Ferula species: Biochemical characteristics, pharmaceutical and industrial applications, and suggestions for biotechnologists. Industrial Crops and Products, 2019. 139: p. 111511.

Saez, N.J. and V. Herzig, Versatile spider venom peptides and their medical and agricultural applications. Toxicon, 2019. 158: p. 109-126.

Leontopoulos, S., et al., Bioactivity potential of polyphenolic compounds in human health and their effectiveness against various food borne and plant pathogens. A review. J. Food Biosyst. Eng, 2017. 7: p. 1-19.

Devi, R., et al., Fungal secondary metabolites and their biotechnological applications for human health, in New and Future Developments in Microbial Biotechnology and Bioengineering. 2020, Elsevier. p. 147-161.

Bonifácio, B.V., et al., Antifungal activity of a hydroethanolic extract from Astronium urundeuva leaves against Candida albicans and Candida glabrata. Frontiers in microbiology, 2019. 10: p. 2642.

Abbas, S. and S. Malla, Cytotoxicity and expression studies of angiogenesis-promoting genes in cancer cell lines under the treatment of cancer candidate drugs. Asian J Pharm Clin Res, 2019. 12(5): p. 130-134.

Praditya, D., et al., Anti-infective properties of the golden spice curcumin. Frontiers in microbiology, 2019. 10: p. 912.

Ficociello, G., et al., Anti-candidal activity and in vitro cytotoxicity assessment of graphene nanoplatelets decorated with zinc oxide nanorods. Nanomaterials, 2018. 8(10): p. 752.

Guillin, O.M., et al., Selenium, selenoproteins and viral infection. Nutrients, 2019. 11(9): p. 2101.

Shrestha, R., et al., Fungus-derived hydroxyl radicals kill hepatic cells by enhancing nuclear transglutaminase. Scientific reports, 2017. 7(1): p. 1-11.

Kawai, T. and S. Akira, Toll-like receptors and their crosstalk with other innate receptors in infection and immunity. Immunity, 2011. 34(5): p. 637-650.

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Published

2021-12-31

How to Cite

Shalal, O. S. (2021). Expression Profiling of Transglutaminase 2 and Inflammatory Host Response in Aspergillus Fumigatus After Treatment with Curcuma Extracts. Journal of Techniques, 3(4), 37–43. https://doi.org/10.51173/jt.v3i4.385

Issue

Section

Medical techniques