Measure the levels of TGF-β in Induced Wound Infection with Staphylococcus aureus

Authors

  • Athraa Hassan Al-Khafaji
  • Kifah Fadhil Al-Shabaa Faculty of Veterinary medicine, University of Kufa, iraq

DOI:

https://doi.org/10.36320/ajb/v14.i1.11741

Keywords:

Animal model, Bacterial Inoculum, Staphylococcus aureus, Wound Infection

Abstract

Aim: Staphylococcus aureus wound infections are the leading cause of mortality and morbidity in patients around the world, Animal models is standard tools for studying a wide range of traumatic wound infections. The present paper is aim to study the effect of Staphylococcus aureus (SA) in wound and how the innate immune system interacts with the  infection , by Measure TGF-β cytokine , and there’s roles on recovery of wound. Methodology : 51 female  albino Rats  were used at the age of  ( 6-9) week , the animals were divided in to three group (17 animal in the group) the healthy control (Group I), wound control group(Group II), and infection contamination group with SA (Group III), , To mimic clinically occurring infections caused by SA infection , excision wound were made on dorsal side of the animals , and SA  2 × 108 (CFU)/mL were inoculated on the wound site in infection contamination group   ,  The blood collected after 24hours post infection for three days (24, 48, 72 hours) , histopathological examination with  ELISA tecinque was made for Measure TGF-β. Result :Immunological assay results of this study showed that the serum level for TGF-beta were  statistical significant between different values at different time when  (P ≤ 0.02).

Conclusion: TGF-β is a potent immunomodulatory that initiates and terminates tissue repair. It is released in wound areas after tissue damage by the inflammatory cell .

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References

Asada, et al., 2012. Novel models for bacterial colonization and infection of full‐thickness wounds in rats. Wound Repair and Regeneration, pp. 601-610. DOI: https://doi.org/10.1111/j.1524-475X.2012.00800.x

Bayir, et al., 2019. "The effects of Beeswax, Olive oil and Butter impregnated bandage on burn wound healing. Burns, pp. 1410-1417. DOI: https://doi.org/10.1016/j.burns.2018.03.004

Cray & Carolyn, 2012. Acute phase proteins in animals. Progress in molecular biology and translational science, pp. 113-150. DOI: https://doi.org/10.1016/B978-0-12-394596-9.00005-6

d'Acampora, et al., 2006. Morphological analysis of three wound-cleaning processes on potentially contamined wounds in rats. Acta cirurgica brasileira, pp. 332-340. DOI: https://doi.org/10.1590/S0102-86502006000500011

Grada, A., Mervis, J. & Falanga, V., 2018. Research techniques made simple: animal models of wound healing. Journal of Investigative Dermatology, pp. 2095-2105. DOI: https://doi.org/10.1016/j.jid.2018.08.005

Jawa, et al., 2011. Analytic review: interleukin-6 in surgery, trauma, and critical care: part I: basic science. Journal of intensive care medicine, pp. 3-12. DOI: https://doi.org/10.1177/0885066610395678

Kennedy, et al., 2010. Targeting of alpha-hemolysin by active or passive immunization decreases severity of USA300 skin infection in a mouse model. The Journal of infectious diseases, pp. 1050-1058. DOI: https://doi.org/10.1086/656043

Khalaf, et al., 2019. "Histopathological, immunohistochemical, and molecular studies for determination of wound age and vitality in rats. International wound journal, pp. 1416-1425. DOI: https://doi.org/10.1111/iwj.13206

Kim, Hwan Keun, Dominique Missiakas & Olaf Schneewind, 2014. Kim, Hwan Keun, Dominique Missiakas, and Olaf Schneewind. "Mouse models for infectious diseases caused by Staphylococcus aureus. Journal of immunological methods, pp. 88-99. DOI: https://doi.org/10.1016/j.jim.2014.04.007

Kim, M. H. et al., 2008. Dynamics of neutrophil infiltration during cutaneous wound healing and infection using fluorescence imaging. Invest Dermatol , pp. 128(7): 1812-1820.. DOI: https://doi.org/10.1038/sj.jid.5701223

Kugelberg, et al., 2005. Establishment of a superficial skin infection model in mice by using Staphylococcus aureus and Streptococcus pyogenes. Antimicrobial agents and chemotherapy, pp. 3435-3441. DOI: https://doi.org/10.1128/AAC.49.8.3435-3441.2005

Levinson, et al., 2014. Review of medical microbiology and immunology. Estados Unidos: McGraw-Hill Medical, pp. 1113-1950.

Levinson, et al., 2014. Review of medical microbiology and immunology. Estados Unidos. McGraw-Hill Medical, pp. 1113-1950.

MacDonald, K. P. et al., 2010. An antibody against the colony-stimulating factor 1 receptor depletes the resident subset of monocytes and tissue-and tumor-associated macrophages but does not inhibit inflammation. The Journal of the American Society of Hematology, pp. DOI: https://doi.org/10.1182/blood-2010-02-266296

(19), 3955-3963.

Malachowa، et al.، 2013. Mouse model of Staphylococcus aureus skin infection." In Mouse Models of Innate Immunity. Humana Press, Totowa, NJ، pp. 109-116. DOI: https://doi.org/10.1007/978-1-62703-481-4_14

Mohammad, et al., 2021. Staphylococcus aureus lipoproteins promote abscess formation in mice, shielding bacteria from immune killing. Communications biology, pp. 1-12. DOI: https://doi.org/10.1038/s42003-021-01947-z

Nayak, Lexley M & Pinto Pereira, 2006. Catharanthus roseus flower extract has wound-healing activity in Sprague Dawley rats. BMC Complementary and Alternative medicine, p. 41. DOI: https://doi.org/10.1186/1472-6882-6-41

Nguyen, V. T., 2015. "Mechanisms of delayed wound healing in various models of human diseases." PhD diss. 6 ed. s.l.:Paris.

Nguyen, V. T., 2015. Mechanisms of delayed wound healing in various models of human diseases. PhD diss., Paris, pp. 18-177.

Pang, Jingbo, Norifumi Urao & Timothy J. Koh, 2020. Proliferation of Ly6C+ monocytes/macrophages contributes to their accumulation in mouse skin wounds. Journal of leukocyte biology, pp. 551-560. DOI: https://doi.org/10.1002/JLB.3HI1119-389RRRR

Pérez, et al., 2021. Comparison of antibacterial activity and wound healing in a superficial abrasion mouse model of Staphylococcus aureus skin infection using photodynamic therapy based on methylene blue or mupirocin or both. Frontiers in Medicine. DOI: https://doi.org/10.3389/fmed.2021.673408

Shankar، M.، B، R.، D، R. K. و M، N. B.، 2014. . "Wound healing and it’s important—a review.". Der Pharmacologia Sinica، pp. 24-30.

Silva, et al., 2013. Low level laser therapy (AlGaInP) applied at 5J/cm2 reduces the proliferation of Staphylococcus aureus MRSA in infected wounds and intact skin of rat. Anais brasileiros de dermatologia, pp. 50-55. DOI: https://doi.org/10.1590/S0365-05962013000100005

Thurlow, Lance R, Gauri S. Joshi & Anthony R. Richardson, 2018. Peroxisome proliferator-activated receptor γ is essential for the resolution of Staphylococcus aureus skin infections. Cell host & microbe, pp. 261-270. DOI: https://doi.org/10.1016/j.chom.2018.07.001

Treuting, P. M., Suzanne, M., Dintzis & Kathle, 2018. Comparative anatomy and histology: a mouse, rat, and human atlas. s.l.:Academic Press.

Tsige, et al., 2020. Prevalence of Methicillin-Resistant Staphylococcus aureus and Associated Risk Factors among Patients with Wound Infection at Referral Hospital, Northeast Ethiopia. Journal of pathogens. DOI: https://doi.org/10.1155/2020/3168325

Wang, et al., 2017. Transforming growth factor β plays an important role in enhancing wound healing by topical application of Povidone-iodine. Scientific reports, pp. 1-8. DOI: https://doi.org/10.1038/s41598-017-01116-5

Yang, et al., 2020. Antimicrobial and anti-inflammatory potential of Angelica dahurica and Rheum officinale extract accelerates wound healing in Staphylococcus aureus-infected wounds. Scientific reports, pp. 1-10. DOI: https://doi.org/10.1038/s41598-020-62581-z

Yeng, et al., 2019. nvestigation of wound healing effect of Acalypha indica extract in sprague dawley rats. Biomedical and Pharmacology Journal, pp. 1857-1865. DOI: https://doi.org/10.13005/bpj/1816

Zaiss, et al., 2019. Immune‐and non‐immune‐mediated roles of regulatory T‐cells during wound healing. Immunology 157, pp. 190-197. DOI: https://doi.org/10.1111/imm.13057

Zhao, et al., 2017. TGF-β1 promotes Staphylococcus aureus adhesion to and invasion into bovine mammary fibroblasts via the ERK pathway. Microbial pathogenesis, pp. 25-29. DOI: https://doi.org/10.1016/j.micpath.2017.01.044

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Published

2022-03-11

How to Cite

Hassan Al-Khafaji, A., & Fadhil Al-Shabaa , K. (2022). Measure the levels of TGF-β in Induced Wound Infection with Staphylococcus aureus. Al-Kufa University Journal for Biology, 14(1), 28–37. https://doi.org/10.36320/ajb/v14.i1.11741

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