Research Article |
Corresponding author: Tsveteslava Ignatova-Ivanova ( tsignatovaivanova@shu.bg ) Corresponding author: Radoslav Ivanov ( rado_cvet@abv.bg ) Corresponding author: Nikolay Natchev ( natchev@shu.bg ) Academic editor: Plamen Peikov
© 2022 Tsveteslava Ignatova-Ivanova, Sevginar Ibryamova, Darina Bachvarova, Seniha Salim, Simona Valkova, Yoanna Simeonova, Dimitar Dimitrov, Radoslav Ivanov, Nesho Chipev, Nikolay Natchev.
This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation:
Ignatova-Ivanova T, Ibryamova S, Bachvarova D, Salim S, Valkova S, Simeonova Y, Dimitrov D, Ivanov R, Chipev N, Natchev N (2022) Determination of the antimicrobial activity of lactic acid bacteria isolated from the Black sea mussel Mytilus galloprovincialis Lamarck, 1819. Pharmacia 69(3): 637-644. https://doi.org/10.3897/pharmacia69..e84850
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The present study reports on the determination of the antimicrobial activity of lactic acid bacteria (LAB) isolated from the Black sea mussel Mytilus galloprovincialis Lamarck, 1819. The samples were collected in the period of August 2018 until March 2021. The BIOLOG system was used for microbiological determination. From the mussel M. galloprovincialis Lam. four species of LAB were isolated - Sporolactobacillus kofuensis, Lactobacillus sakei, Streptococcus gallolyticus ss gallolyticus and Lactibacillus brevis. The activity of the strains was determined against test cultures (Escherichia coli 3398, Staphylococus aureus 745, Bacillus subtilis 6633, Salmonella typhimurium 3591, Listeria monocytogens 863 Enterobacter aerogenes 3691, Aspergillus niger, Penicillium claviforme, Saccharomyces cerevisae, Candida albicans 8673 and Candida glabrata 72). Before the analysis for antimicrobial activity, the LAB were cultured in media with different concentrations of sugars - 2, 5 and 10%. The results showed that 4 strains S. kofuensis, L. sakei, S. gallolyticus ss gallolyticus and L. brevis cultured on glucose and oligosaccharides completely lost their activity in all studied variants. Therefore, some carbohydrates (glucose) and oligosaccharides induce the synthesis outside the cell of biologically active molecules, which can probably be attributed to peptides/proteins.
antimicrobial activity, bacteriocins, Black Sea, lactic acid bacteria, Mytilus galloprovincialis Lam
Тhe consumption of safe food is a significant social problem in the modern world.Worldwide bivalve production has consistently increased over the years from 7.1 million in 1995 to 16.1 million in 2014, and the consumer demand is expected to further increase in the next future
The aim of the present study was to determine the antimicrobial activity of lactic acid bacteria (LAB) isolated from the Black Sea mussel Mytilus galloprovincialis Lam. with a view to their use either as safe bioconservatives for seafood in food storage or as a way to protect black mussels from various pathogens present in their habitat.
The study was conducted at the Department of Biology, University of Shumen, Bulgaria, from August 2018 until March 2021.The samples were collected from the regions of Mussel farm – Kavarna 43.4108°N, 28.3566°E; Port Varna 43.1880°N, 27.9113°E; Sozopol; 42.4005°N, 27.7202°E; Tyulenovo 43.4836°N, 28.5810°E; Constanta 44.1747°N, 28.6583°E (Fig.
After collection, the samples (about 10 kg) were immediately refrigerated (4 °C) and transported to the laboratory for the analyses.
Three subsamples (each of about 1 kg of mussels) were used for the microbiological analyses. The mussels were scrubbed free of dirt, washed in hypochlorite solution (20 mg l-1), rinsed with sterile distilled water, and shucked with a sterile knife. The whole soft tissue of the mussel’sliquor samples (about 100 g) were homogenized. Lactic acid bacteria (LAB) were isolated in media of MRS (de Mann Rogosa Sharpe, Biolife 272-20128, Milano, Italia). The strains were cultured overnight (16–18 h) on MRS at 37 °C and in limitation of oxygen (tubes or Petri dishes with the strains were incubated in plastic bags, which limited the oxygen content).
Since high concentrations of sugars and oligosaccharides stimulate the synthesis of bacteriocins and increase the antimicrobial activity of ICD (
LAB were grown in MRS broth (Merck). Overnight grown cells were washed twice in saline (0.85% NaCl solution), and 10% of the bacterial suspension (107 cfu ml-1) was used to inoculate modified MRS broth and agar medium (pH 6.8) containing either 2,5 and 10% glucose, 2,5 and 10% GOS (glucooligosaccharides), 2,5 and 10% FOS (fructooligosaccharides). The anaerobic fermentations were performed in 100 ml glass bottles at 37 °C for 48 h (BBL Gas Pak anaerobic system envelopes).
The microbial identification was performed by the Biolog Microbial Identification System VIO45101AM. The isolated strains were screened on BL4021502 Tryptic Soy Agar (TCA), cultured for 24 hours at 37 °C and then subjected to Gen III plaque identification to identify Gram positive and Gram negative aerobic bacteria. The microscopic pictures were performed using stereomicroscope OPTIKA (Italy) with a DinoEye, Eyepiece camera with 5 megapixels. The photographs were performed by using a Canon EOS 60D camera. The GEN III MicroPlate test panel provides a standardized micromethod using 94 biochemical tests to profile and identify a broad range of Gram-negative and Gram-positive bacteria. Biolog’s Microbial Identification Systems software (e.g. OmniLog Data Collection) is used to identify the bacterium from its phenotypic pattern in the GEN III MicroPlate. The Biologsystem allows to quickly and accurately identify more than 2900 species of aerobic and anaerobic bacteria, yeasts, and fungi. Biolog’s advanced phenotypic technology provides valuable information on the properties of the strains, in addition to species-level identification. Biolog’s carbon technology identifies the environment and pathogenic microorganisms by producing a characteristic pattern or “metabolic fingerprint” of discrete test reactions performed in a 96-well microplate. The culture suspensions are tested with a panel of pre-selected assays, then incubated, read and compared with extensive data-bases. https://www.biolog.com/products-portfolio-overview/microbial-identification.
Escherichia coli 3398 NBIMCC, Staphylococusaureus 745 NBIMCC, Bacillus subtilis 6633 ATCC, were obtained American Type, Culture Collection (ATCC), Salmonella typhimurium 3591 NBIMCC, Listeria monocytogens 863 NBIMCC, Enterobacter aerogenes 3691 NBIMCC, Aspergillus niger NBIMCC, Penicillium claviforme NBIMCC, Saccharomyces cerevisae NBIMCC, Candida albicans 8673 NBIMCC and Candida glabrata 72 NBIMCC were obtained from the National Bank for Industrial Microorganisms and Cell Cultures, Sofia, Bulgaria (NBIMCC). All the isolates were checked for purity and maintained in slants of Nutrient agar. The test organisms were propagated in appropriate media as follows: Escherichia coli grown on LB (Luria-Bertani) agar medium (Sigma, St. Louis, MO), Listeria monocytogens 863 grown on BH (Brain Heart)-agar medium (Biokar Diagnostics, Beauvais, France), Salmonella typhimurium grown on Elliker, and Bacillus sp. grown on nutrition broth and agar.
Antimicrobial assay was performed by the well diffusion method using soft 2% agar. Agar medium was added to sterile Petri dishes seeded with 100 µl of each test bacterial strains. Wells of equal distance were dug on the seeded plates. Each well was filled up with 100 µl of exponential Lactobacillus cultures in mMRS broth were used as inoculum for the antifungal tests. After adjusting the pH at 6.5 by NaOH, the activity of the plant extracts was checked. The plates were incubated at 37 °C for 48 hours. The antibacterial activity was assayed by measuring the diameter of the inhibition zone formed around the well (
Effects of heat and hydrolytic enzymes (trypsin from Sigma, No. T-8253; proteinase K from Sigma, No. P-0390) on bacteriocin activity were determined according to (
The microorganisms were isolated from M. galloprovincialis Lam collected from five localities of the north and south Bulgarian Black Sea aquatory and the region of Constanta, Romania. After 24 h of cultivation on different media, various microbial colonies were obtained. The species of microorganisms were confirmed not only on selective media, but also by the results of the BIOLOG system.
The results of the antimicrobial activity test for each LAB species are represented in Figs
From the data in figure 2 it is evident that the species St. gallolyticus ss gallolyticus has the highest zone of inhibition relative to E. aerogenes 3691 when culturing 2% FOSs. Relatively high zones of inhibition were also observed against E. coli 3398, S. aureus 745, B. subtilis 6633 and L. monocytogens 863 in the cultivation of 5% FOSs. In the cultivation of the strain on GOS activity was observed against E. aerogenes 3691, E. coli 3398, S. aureus 745, B. subtilis 6633 and L. monocytogens 863, the highest being against B. subtilis 6633. Compared to S. typhimurium 3591, molds and fungi have no areas of activity.
The data represented in Fig.
The data in Fig.
From the data in Fig.
To clarify the nature of the biologically active components, neutralized cell supernatants treated with trypsin and proteinase K were used. The results obtained are shown in Tables
Effect of enzymes and temperature on the inhibitory activity of supernatants of L. brevis and L. sakei.
Strain | After cultivation on FOS (mm sterile zone) | After cultivation on GOS (mm sterile zone) | After cultivation on glucose (mm sterile zone) | |||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
control | temperature | Tripsin | proteinase K | control | temperature | Tripsin | proteinase K | control | temperature | Tripsin | proteinase K | |
L. brevis | 31.9 | no zone | no zone | no zone | 8 | no zone | no zone | no zone | 10 | no zone | no zone | no zone |
L. sakei | 37.5 | no zone | no zone | no zone | 19,74 | no zone | no zone | no zone | 11 | no zone | no zone | no zone |
The results of Tables
Effect of enzymes and temperature on the inhibitory activity of St. gallolyticus and Sp. kofuensis.
Strain | After cultivation on FOS (mm sterile zone) | After cultivation on GOS (mm sterile zone) | After cultivation on glucose (mm sterile zone) | |||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
control | temperature | Tripsin | proteinase K | control | temperature | Tripsin | proteinase K | control | temperature | Tripsin | proteinase K | |
St. gallolyticus | 47.85 | no zone | no zone | no zone | 19.74 | no zone | no zone | no zone | 18.87 | no zone | no zone | no zone |
Sp. kofuensis | 26.9 | no zone | no zone | no zone | 33.45 | no zone | no zone | no zone | 9 | no zone | no zone | no zone |
Mussels can filter up to 10 liters of water per hour (
A review of the available literature reveal, that several probiotics alone or in combination can increase both systemic and local immunity in fish (
There is much evidence in the literature that excessive use of antibiotics in the fight against pathogenic bacteria has led to the emergence of high levels of microbial resistance, which poses new challenges to human health (
The marine environment is extremely hydrophilic and contains not only a wide range of microorganisms but also a high salt content. The marine environment is constituted by approximately 106 bacteria/mL and 109 virus/mL of seawater and, thus, represents a rich source of pathogens (
The antimicrobial activity of AMPs is based on their initial electrostatic interaction with the negatively charged surface of bacteria and thus, the free ions produced by the high environmental concentrations of salt characteristic of some diseases could reduce the interaction and antimicrobial activity. Marine AMPs have evolved to adapt to high salt concentrations in seawater. Marine organisms are therefore a promising source of new bioactive substances for the development of therapeutic agents. There is evidence in the literature for the isolation of AMPs from different marine organisms - different species of fish, crabs, shrimps, jellyfish and sea urchin (
Seawater is a rich and as yet undiscovered source of bioactive molecules for the development of new drugs against microbial pathogens in the current situation of growing antimicrobial resistance. In this regard, marine microorganisms and in particular mussels live in extreme and stressful environments and can become a rich source of templates for the design of new antimicrobial peptides that could become effective drugs for human and veterinary medicine. These are the first results published in the literature on the presence of lactic acid bacteria which exhibit probiotic properties in the microflora of the black mussel in the Bulgarian Black Sea. Our results are extremely important because if these strains successfully ferment oligosaccharides and at the same time produce biologically active substances, they would be important for the functions of the intestinal microflora of seafood consumers and for the protection of mussels from other pathogenic bacteria. The isolated strains may also possess the potential also be used in cosmetics industry.
The contributors express their gratitude for the funding by fund scientific research Bulgaria programme grant KP-06-H21/7/18 Dec 2018, the project by Shumen University project 08-80/09.02.2022 Department of Biology.