Exploring Listeria monocytogenes in Ewe Milk: ssrA Gene-based Real-time PCR Identification, Phylogenetic Analysis, and Antibacterial Assessment of Magnesium Oxide Nanoparticles Synthesized with Myrtus communis Leaf Extract

Jenan Nadhim Sadeq, Balsam Miri Mizher, Alyaa Abdulhussein Alsaedi, Ola Hakim Khudhair

Abstract


Background: Listeria monocytogenes, a zoonotic pathogen affecting humans and animals, exhibits a global distribution, including Iraq. This study focused on the rapid identification and phylogenetic analysis of L. monocytogenes in freshly collected ewe milk samples from various farms in Al-Qadisiyah province, Iraq.

Methods: The study was conducted with care and precision, involving 150 milk samples. These samples were subjected to traditional bacterial isolation and identification using the enrichment culture method and biochemical tests, with the PCR technique confirming the results. The antibacterial activity of MgONPs was then assessed using the disc diffusion method, ensuring a comprehensive and reliable approach to the study.

Result: The results show that 150 ewe milk samples underwent real-time PCR (RT-PCR) targeting the ssrA gene, followed by partial 16S rRNA gene sequencing (PSGS) of purified conventional PCR products. Furthermore, the study entails the biosynthesis of magnesium oxide nanoparticles using Myrtus communis  leaf extract, followed by a comprehensive characterization utilizing UV-spectra, FTIR, SEM, and TEM techniques. The Agar well diffusion method assessed the antibacterial efficacy of these Biosynthesized nanoparticles against L. monocytogenes. The RT-PCR results revealed the presence of L. monocytogenes in 36 out of 150 samples (24%). Subsequent PCR analysis confirmed the presence of the pathogen in 30 out of these 36 positive samples (83.33%). Sequencing of two purified PCR products demonstrated 100% nucleotide identity with global isolates from Iraq and Turkey. Furthermore, the study demonstrated that L. monocytogenes exhibited substantial sensitivity (24.66 ± 0.3) to the biosynthesized magnesium oxide nanoparticles. These findings underscore the speed and precision of the RT-PCR method for detecting L. monocytogenes in fresh ewe milk samples.

Conclusion: This comprehensive investigation enhances our understanding of L. monocytogenes prevalence in ewe milk and highlights the potential of Myrtus communis -derived nanoparticles for combating this pathogen.

Keywords: Antibacterial nanoparticles; Listeria monocytogenes; Magnesium oxide; Myrtus communis  sheep milk; ssrA gene  


Full Text:

PDF

References


ECDC, EFSA. The European Union One Health 2019 Zoonoses Report. European Food Safety Authority Journal, (2019); 17(12): e05926.

Quereda JJ, Leclercq A, Moura A, Vales G, Gómez-Martín Á, et al. Listeria valentina sp. nov., isolated from a water trough and the faeces of healthy sheep. International Journal of Systematic and Evolutionary Microbiology, (2020); 70(11): 5868–79.

Charlier C, Disson O, Lecuit M. Maternal-neonatal listeriosis. Virulence, (2020); 11(1): 391–7.

NicAogáin K, O’Byrne CP. The Role of Stress and Stress Adaptations in Determining the Fate of the Bacterial Pathogen Listeria monocytogenes in the Food Chain. Frontiers in Microbiology, (2016); 7(11): 1865.

Radoshevich L, Cossart P. Listeria monocytogenes: towards a complete picture of its physiology and pathogenesis. Nature Reviews Microbiology, (2018); 16(1): 32–46.

Schlech WF. Epidemiology and Clinical Manifestations of Listeria monocytogenes Infection. Microbiology Spectrum, (2019); 7(3): 1–12.

Al-Nabulsi A, Al-Holy MA, Shahbaz HM, Alimat AN, Abu Ghoush MH, et al. Emergence of antibiotic resistance in Listeria monocytogenes isolated from food products: a comprehensive review. Comprehensive Reviews in Food Science and Food Safety, (2018); 17(5): 1277-92.

Anand U, Carpena M, Kowalska-Góralska M, Garcia-Perez P, Sunita K, et al. Safer plant-based nanoparticles for combating antibiotic resistance in bacteria: A comprehensive review on its potential applications, recent advances, and future perspective. Science of The Total Environment, (2022); 821: 153472.

Castillo-Henríquez L, Alfaro-Aguilar K, Ugalde-Álvarez J, Vega-Fernández L, Montes de Oca-Vásquez G, et al. Green synthesis of gold and silver nanoparticles from plant extracts and their possible applications as antimicrobial agents in the agricultural area. Nanomaterials, (2020); 10(9): 1763.

Soni V, Raizada P, Singh P, Cuong HN, Rangabhashiyam S, et al. Sustainable and green trends in using plant extracts for the synthesis of biogenic metal nanoparticles toward environmental and pharmaceutical advances: A review. Environmental Research, (2021); 202: 111622.

Ramrakhiani L, Ghosh S. Metallic nanoparticle synthesised by biological route: safer candidate for diverse applications. IET Nanobiotechnology, (2018); 12(4): 392-404.

MacFaddin JF. Biochemical tests for identification of medical bacteria. Williams and Wilkins, Philadelphia, PA, 2000; 113(7).5

Gasanov U, Hughes D, Hansbro PM. Methods for the isolation and identification of Listeria spp. and Listeria monocytogenes: a review. FEMS Microbiology Reviews, (2005); 29(5): 851–75.

Navas J, Ortiz S, Lopez P, Jantzen MM, Lopez V, et al. Evaluation of Effects of Primary and Secondary Enrichment for the Detection of Listeria monocytogenes by Real-Time PCR in Retail Ground Chicken Meat. Food Control, (2007); 3(4). 347-54.

Heo EJ, Song BR, Park HJ, Kim YJ, Moon JS, et al. Rapid Detection of Listeria monocytogenes by Real-Time PCR in Processed Meat and Dairy Products. Journal of Food Protection, (2014); 77(3): 453–58.

Lan ZW, Xiao MJ, Guan YL, Zhan YJ, Tang XQ. Detection of Listeria monocytogenes in a patient with meningoencephalitis using next-generation sequencing: a case report. BMC Infectious Diseases, (2020); 20(1): 721.

Wagner E, Fagerlund A, Langsrud S, Møretrø T, Jensen MR, et al. Surveillance of Listeria monocytogenes: Early Detection, Population Dynamics, and Quasimetagenomic Sequencing during Selective Enrichment. Applied and Environmental Microbiology, (2021); 87(24): e01774-21.

Crowther CV, Hilton SH, Kemp LK, Hayes MA. Isolation and Identification of Listeria monocytogenes Utilizing DC Insulator-based Dielectrophoresis. Analytica Chimica Acta, (2019); 1068(8): 41–51.

Amagliani G, Giammarini C, Omiccioli E, Brandi G, Magnani M. Detection of Listeria monocytogenes using a commercial PCR kit and different DNA extraction methods. Food Control, (2007); 18(9): 1137–42.

Churchill RLT, Lee H, Hall JC. Detection of Listeria monocytogenes and the toxin listeriolysin O in food. Journal of Microbiological Methods, (2006); 64(2): 141–170.

Jin D, Luo Y, Zhang Z, Fang W, Ye J, Wu F, Ding G. Rapid molecular identification of Listeria species by use of real-time PCR and high-resolution melting analysis. FEMS Microbiology Letters, (2012); 330(1): 72–80.

Krypuy M, Newnham GM, Thomas DM, Conron M, Dobrovic A. High resolution melting analysis for the rapid and sensitive detection of mutations in clinical samples: KRAS codon 12 and 13 mutations in non-small cell lung

cancer. BMC Cancer, (2006); 6(12): 295.

Liu D. Identification, subtyping and virulence determination of Listeria monocytogenes, an important foodborne pathogen. Journal of Medical Microbiology, (2006); 55(Pt 6): 645–59.

Price EP, Smith H, Huygens F, Giffard PM. High-resolution DNA melt curve analysis of the clustered, regularly interspaced short-palindromic-repeat locus of Campylobacter jejuni. Applied and Environmental Microbiology, (2007); 73(10): 3431–36.

Bhagwat AA. Simultaneous detection of Escherichia coli O157:H7, Listeria monocytogenes and Salmonella strains by real-time PCR. International Journal of Food Microbiology, (2003); 84(2): 217–24.

Terentjeva M, Šteingolde Ž, Meistere I, Elferts D, Avsejenko J, et al. Prevalence, genetic diversity and factors associated with distribution of Listeria monocytogenes and other Listeria spp. in cattle farms in Latvia. Pathogens, (2021); 10(7): 851.

Swetha CS, Porteen K, Elango A, Ronald BS, Kumar TS, et al. Genetic diversity, virulence and distribution of antimicrobial resistance among Listeria monocytogenes isolated from milk, beef, and bovine farm environment. Iranian Journal of Veterinary Research, (2021); 22(1): 1.

Sharma SK, Khan AU, Khan M, Gupta M, Gehlot A, Park S, Alam M. Biosynthesis of MgO nanoparticles using Annona squamosa seeds and its catalytic activity and antibacterial screening. Micro & Nano Letters, (2020); 15(1): 30-4.

Balakrishnan G, Velavan R, Batoo KM, Raslan EH. Microstructure, optical and photocatalytic properties of MgO nanoparticles. Results in Physics, (2020); 16: 103013.

Dutta G, Sugumaran A. Bioengineered zinc oxide nanoparticles: Chemical, green, biological fabrication methods and its potential biomedical applications. Journal of Drug Delivery Science and Technology, (2021); 66: 102853.

Mehrdel B, Yehya AHS, Dheyab MA, Jameel MS, Aziz AA, et al. The antibacterial and toxicological studies of mycosynthesis silver nanoparticles by isolated phenols from Agaricus bisporus. Physica Scripta, (2023); 98(12): 125007.

Jameel MS, Aziz AA, Dheyab MA, Khaniabadi PM, Kareem AA, et al. Mycosynthesis of ultrasonically-assisted uniform cubic silver nanoparticles by isolated phenols from Agaricus bisporus and its antibacterial activity. Surfaces and Interfaces, (2022); 29: 101774.

Alavi M, Rai M. Recent advances in antibacterial applications of metal nanoparticles (MNPs) and metal nanocomposites (MNCs) against multidrug-resistant (MDR) bacteria. Expert Review of Anti-infective Therapy, (2019); 17(6): 419-28.




DOI: http://dx.doi.org/10.62940/als.v11i3.2905

Refbacks

  • There are currently no refbacks.