Asessment of antibacterial activity of bacteria immunized Muga silkworm (Antheraea assamensis Helfer) and its comparison with market antibiotics

Paper Details

Research Paper 08/08/2023
Views (341) Download (46)
current_issue_feature_image
publication_file

Asessment of antibacterial activity of bacteria immunized Muga silkworm (Antheraea assamensis Helfer) and its comparison with market antibiotics

Shibani Kalita, Tanushree Biswas, Ankita Devi , Sanghamitra Saharia, Dimpimoni Kalita, Sunayan Bardoloi
Int. J. Biosci.23( 2), 220-227, August 2023.
Certificate: IJB 2023 [Generate Certificate]

Abstract

The Muga silkworm, Antheraea assamensis Helfer, which plays a huge role in the socio-economic scenario of Assam is susceptible to a wide range of infections due to the outdoor rearing of  these silkworms. Infection or injury triggers the immune response of their body, which involves several components including the production of some antimicrobial proteins for defense against the invading microorganism. The current study deals with the immunization of the Muga silkworms with Bacillus thuringiensis to observe the response of the activated haemolymph against E. coli and B. thuringiensis. Analysis was carried out to compare the antibacterial activity of the immunized haemolymph with that of three common market antibiotics, Levofloxacin, Azithromycin and Rifaximin. After immunization, haemolymph was procured at different time intervals i,e 6 hours, 12 hours, 18 hours and 24 hours and each time interval was taken as a different group along with one control group. Analysis for total protein and free amino acid for all groups were carried out which showed increase in protein and free amino acid concentration in all groups as compared to the control haemolymph samples. No antimicrobial action was shown by the samples obtained at 6 hours, 12 hours and 18 hours with only the immunized haemolymph obtained after 24 hours showed positive activity against both B. thuringiensis as well as E.coli along with potency almost at par with the antibiotics taken for the study. Thus, the study revealed clear roles of bacteria immunized haemolymph to fight against infections and proper characterization of the components of the immunized haemolymph might lead to more specific understanding of such immune mechanisms as well as their role as future antibiotics.

VIEWS 50

Adamo SA. 2004. Estimating disease resistance in insects: Phenoloxidase and lysozyme-like activity and disease resistance in the cricket Gryllus texensis. Journal of Insect Physiology 50, 209-216. https:// doi.org/10.1016/j.jinsphys.2003.11.011

Browne K, Chakraborty S, Chen R, Willcox MD, Black DS, Walsh WR, Kumar NA. 2020. New Era of Antibiotics: The Clinical Potential of Antimicrobial Peptides. International Journal of Molecular Sciences 21(19), 7047.

El-Sadawy HA, Abou-Nour AA, Sobh HA, Ghally SE. 2009. Biochemical Changes in Parasarcophaga. aegyptiaca and Argas (persicargas) persicus Haemolymph Infected with Entomopathogenic Nematode. Nature and Science 7(6), 70-81.

Florkin M, Jeuniaux C. 1974. Haemolymph composition. In the physiology of insecta. Roskstein, M.ed 5, 255-307.

Gad AA. 2012. Immune responses of Bombyx mori larvae towards the bacterial infections with Escherichia coli and Bacillus thuringeinsis. The Egyptian Science Magazine 7(3, 4), 1-5.

Haloi K, Kalita M, Nath R, Devi D. 2016. Characterization and pathogenicity assessment of gut-associated microbes of muga silkworm Antheraea assamensis Helfer (Lepidoptera: Saturniidae). Journal of Invertebrate Pathology 138, 73-85. https://doi.org/10.1016/j.jip.2016.06.006

Hoffmann JA. 1995. Innate immunity of insects. Current Opinion in Immunology 7(1), 4-10. https://doi.org/10.1016/0952-7915(95)80022-0

Lavine MD, Strand MR. 2001. Surface characteristics of foreign targets that elicit an encapsulation response by the moth Pseudoplusia includens. Journal of Insect Physiology. 47(9), 965-974. https://doi.org/10.1016/S0022-1910(01)00071-

Lavine MD and Strand MR. 2002. Insect hemocytes and their role in immunity. Insect biochemistry and molecular biology 32(10), 1295-1309.  https://doi.org/10.1016/S0965-1748(02) 000

Lavine MD, Strand MR. 2003. Haemocytes from Pseudoplusia includens express multiple α and β integrin subunits. Insect molecular biology 12(5), 441-452. https://doi.org/10.1046/j.1365-2583 .2003

Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. 1951. Protein measurement with the Folin phenol reagent. Journal of biological chemistry 193, 265-275.

Moore S and Stein WH. 1968. A modified ninhydrin reagent for the photometric determination of amino acids and related compounds. Journal of Biological Chemistry 211, 907-913.

Neog K, Gogoi SN, Chakravorty R. 2005. Present status and constraints of muga silkworm host plant germplasm conservation. In: Proceedings of the Workshop on Strategies for Maintenance of Non-Mulberry Silkworm and Host Plant Germplasm Held at Central Muga Eri Research & Training Institute, Lahdoigarh, Jorhat, Assam, India pp.1-10.

Portelinha J, Angeles-Boza AM. 2021. The Antimicrobial Peptide Gad-1 Clears Pseudomonas aeruginosa Biofilms under Cystic Fibrosis Conditions. Chem Bio Chem 22(9), 1646-1655. https://doi.org/10.1002/cbic.202000816

Ribeiro C, Brehelin M. 2006. Insect haemocytes: What type of cell is that? Journal of Insect Physiology 52(5), 417-429. https://doi.org/10.1016 /j.jinsphys. 2006.01.005

Saito A, Ueda K, Imamura M, Miura N, Atsumi S, Tabunoki H, Sato R. 2004. Purifiction and cDNA cloning of a novel antibacterial peptide with a cysteinestabilized αβ motif from the longicorn beetle, Acalolepta luxuriosa. Developmental and Comparative Immunology 28, 1-7. https://doi.org/ 10.1016 /S0145-305X(03)00088-0

Schafer S, Aavani F, Kopf M, Drinic A, Sturmer EK, Fuest S, Grust ALC, Gosau M, Smeets R. 2023. Silk proteins in reconstructive surgery: Do they possess an inherent antibacterial activity. A systematic review. Wound Repair and Regeneration 31(1), 99-110. https://doi.org /10.1111

Sharma J, Yadav A, Unni BG, Kalita MC. 2005. Antibacterial proteins from non-mulberry silkworms against flacherie causing Pseudomonas aeruginosa AC-3. Current Science pp. 1613-1618.

Silver LL. 2011. Challenges of antibacterial discovery. Clinical Microbiology Reviews 24, 71-109. https://doi.org/10.1128/cmr.00030-10

Singh RN, Bajpeyicm, Tikader A, Saratchandra B. 2013. Muga Culture. S.B. Nagia, A.P.H. Publishing Corporation pp. 198-351.

Tacconelli E, Carrara E, Savoldi A, Harbarth S, Mendelson M, Monnet DL, Pulcini C, Kahlmeter G, Kluytmans J, Carmeli Y. 2018. Discovery, research, and development of new antibiotics: The WHO priority list of antibiotic-resistant bacteria and tuberculosis. Lancet Infectious Diseases 18, 318-327. https://doi.org/10.1016/S1473-3099(17)30753-3

Wang YP, Lai R. 2010. Insect antimicrobial peptides: structures, properties and gene regulation. Dongwuxue Yanjiu 31(1), 27-34. https://doi.org /10.3724 /sp.j.1141.2010.01027