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Objectives Cancer is the most common cause of death every year. Moreover, high incidence of bacterial resistance to the most frequently used antibiotics contributes a significant death and disability worldwide. Hence, formulation of novel antimicrobial and anticarcinogenic agents is required. Methods In the current study, the antibacterial efficiency of clove extracts (acetonic, dichloromethane, ethanolic, and petroleum ether) against four pathogenic bacterial strains [Escherichia coli, Salmonella typhi, Staphylococcus aureus and Methicillin-resistant Staphylococcus aureus (MRSA)] was estimated by disc diffusion method. Furthermore, the anticancer potency of S. aromaticum extracts against HCT human colon carcinoma was appraised using MTT assay. The phytochemical ingredients of the most effective extract were determined using gas chromatography–mass spectrometry (GC–MS) analysis. Results and conclusion The dichloromethane extract presented the highest antibacterial potency against the pathogenic isolates recording minimum inhibitory concentration (MIC) of 1 mg/disc against MRSA strain and 0.5 mg/disc against both of E. coli and S. typhi strains. Furthermore, the minimum bactericidal concentration (MBC) of clove dichloromethane extract was recoded at 2 mg/disc against MRSA stain, and 1 mg/disc against E. coli and S. typhi strains. The dichloromethane extract of clove showed the lowest cytotoxic activity against HCT cell line whereas, the ethanolic extract exerted the highest efficacy with relative IC50 of 6.71 and 2.53 µg/ml respectively. GC–MS analysis revealed that the clove dichloromethane extract was comprised of eugenol (50.65%) and eugenyl acetate (12.54%) as major active components. In conclusion, clove extracts could be utilized as potential antibacterial and anticarcinogenic agents.

Background Saprolegniasis often cause a significant economic losses to fish hatchery and intensive fish industry. The treatment of saprolegnoid diseases with malachite green seems to have harmful effect and is considered as a mutagenic and carcinogenic substance. The teratogenic and carcinogenic potential of malachite green increased the necessity to find an effective alternative treatment to control the disease. Methods In the present study, seven fungicides used in agriculture were investigated to control Saprolegnia parasitica and S. diclina in vitro. The antifungal activity of each fungicide was compared with that of malachite green as reference fungicide using food poisoning technique. Fish toxicity of the effective fungicides was performed to detect the most applicable fungicides in fish aquarium. Results Four of seven fungicides were found to be effective against the two saprolegnoid fungi. Azoxystrobin and metalaxyl were the most effective fungicides inhibited fungal growth of the two saprolegnoid fungi completely at concentration of 200 ppm and 250 ppm respectively while cyazofamid and etridiazole were moderately effective. Acute toxicity assay of the two effective fungicides showed metalaxyl was low toxic to fish with LC50 of 360 ppm while azoxystrobin was 225 ppm. Hence, it was confirmed that 200 and 250 ppm of azoxystrobin and metalaxyl which completely inhibited mycelial growth of the saprolegniod fungi could be safely used for saprolegniasis control. Conclusion These fungicides which proved to be effective and fishery safer may be applicable as a aquatic fungicides avoiding teratogenic and carcinogenic risk of malachite green.

Alfalfa mosaic virus (AMV) is a worldwide distributed virus that has a very wide host range and causes significant crop losses of many economically important crops, including potato (Solanum tuberosum L.). In this study, the antiviral activity of Bacillus licheniformis strain POT1 against AMV on potato plants was evaluated. The dual foliar application of culture filtrate (CF), 24 h before and after AMV-inoculation, was the most effective treatment that showed 86.79% reduction of the viral accumulation level and improvement of different growth parameters. Moreover, HPLC analysis showed that a 20 polyphenolic compound was accumulated with a total amount of 7,218.86 and 1606.49 mg/kg in POT1-treated and non-treated plants, respectively. Additionally, the transcriptional analysis of thirteen genes controlling the phenylpropanoid, chlorogenic acid and flavonoid biosynthetic pathways revealed that most of the studied genes were induced after POT1 treatments. The stronger expression level of F3H, the key enzyme in flavonoid biosynthesis in plants, (588.133-fold) and AN2, anthocyanin 2 transcription factor, (97.005-fold) suggested that the accumulation flavonoid, especially anthocyanin, might play significant roles in plant defense against viral infection. Gas chromatography-mass spectrometry (GC-MS) analysis showed that pyrrolo[1,2-a]pyrazine-1,4-dione is the major compound in CF ethyl acetate extract, that is suggesting it acts as elicitor molecules for induction of systemic acquired resistance in potato plants. To our knowledge, this is the first study of biological control of AMV mediated by PGPR in potato plants.

Vulvovaginal candidiasis is a common health problem affecting about 75% of women at reproductive age. Teratogenicity and fetal toxicity resulting from antifungal therapy during pregnancy necessitates formulation of novel therapeutic agents. Disk diffusion method was performed to evaluate the antifungal activity of Mentha longifolia extracts against different candidal strains. Moreover, the anticancer activity of different M. longifolia extracts against MCF7 breast cancer cell line was evaluated by MTT assay. The M. longifolia n-hexane extract exhibited the highest antifungal activity, while the methanolic extract showed no antimicrobial activity against the tested Candida strains. Minimum inhibitory concentration (MIC) of n-hexane extract was 250 µg/disk against C. tropicalis while it was 500 µg/disk against C. albicans and C. glabrata. Minimum fungicidal concentration (MFC) was 0.5 mg/disk against C. albicans and C. tropicalis, and 1 mg/disk against C. glabrata. GC–MS analysis of the n-hexane extract was performed to detect the active phytochemical components. Menthone (18.37%) was the main phytochemical active component of n-hexane extract followed by butyloctanol (16.13%), 1,5-(1-Bromo-1-methylethyl)-2-methyl-2-cyclohexen-1-one (14.89%), α-tocopherol (13.13%), eugenol (12.21%), α-resorcylamide (11.56%), citronellal (3.71%), butylated hydroxytoluene (3.21%), isocaryophyllene (2.81%), 2-hexyldecanol (2.12%) and tau-cadinol (1.87%). The methanolic extract exhibited the highest anticancer activity against MCF7 breast cancer cell line while diethyl ether extract exhibited the lowest activity with IC50 of 91.67 and 244.70 µg/ml respectively. M. longifolia extracts could be used as a potential source of novel anticandidal and anti-carcinogenic therapeutic agents. Keywords: Vulvovaginal candidiasis, Mentha longifolia, Anti-candida, Minimum inhibitory concentration, Cytotoxicity, Phytochemicals

Objectives A high incidence of stalk rot disease of maize causes huge economic losses as well as deleterious effects on the environment and human health resulting from fungicide use. Against this background, the current study was established to evaluate the antagonistic efficacy of Trichoderma viride and Trichoderma harzianum strains against Fusarium proliferatum and Fusarium verticillioides strains, the most common causative agents of stalk rot disease of maize. Methods Dual culture assay was performed to determine the antagonistic efficacy of Trichoderma strains against some fusarial pathogens of maize. Mycoparasitic relationships of the antagonistic fungal strains against fungal pathogens were investigated using a slide culture technique. Furthermore, a food poisoning technique was performed to detect the antimycotic efficacy of Trichoderma culture filtrates against fusarial pathogens of maize. Antifungal activity of organic solvent extracts of T. harzianum and T. viride was evaluated using the disc diffusion method. GC–MS analysis was used to detect the active components of these extracts. Results and conclusion Trichoderma viride showed antagonistic activity against F. proliferatum and F. verticillioides with mycelial inhibition rates of 80.17% and 70.46%, while T. harzianum exhibited rates of 68.38% and 60.64%, respectively. The culture filtrates of T. viride and T. harzianum strains exhibited antifungal activity against F. verticillioides strain with suppressive rates of 56.7% and 32.2%, while the mycelial inhibition rates against F. proliferatum strain were 44.09% and 23.50%, respectively. Mycoparasitic action of T. harzianum strain against fusarial strains was detected, while no mycoparasitism was observed between T. viride and fungal pathogens. The fungicidal concentration of carbendazim fungicide against F. proliferatum was 2.00 ppm, while F. verticillioides strain exhibited resistance to carbendazim fungicide. Moreover, the acetonic extracts of T. viride and T. harzianum strains exerted the highest antifungal potency against F. proliferatum strain, recording minimum inhibitory concentrations of 0.25 and 0.50 mg/ml, respectively. The main bioactive constituents of the acetonic extracts of T. viride and T. harzianum strains were palmitic acid (22.87%) and acetic acid (21.36%), respectively. In conclusion, the antagonistic strains could be a potential source of novel biological fungicides, especially against carbendazim-resistant F. verticillioides strain, avoiding side effects of chemical fungicides.

Presently, the bioprocessing of agricultural residues to various bioactive compounds is of great concern, with the potential to be used as plant growth promoters and as a reductive of various diseases. Lycopersiconesculentum, one of the most consumed crops in the human diet, is attacked by Fusarium wilt disease, so the main aim is to biocontrol the pathogen. Several fungal species were isolated from decayed maize stover (MS). Trichodermaasperellum was chosen based on its organic acid productivity and was molecularly identified (GenBank accession number is MW195019). Citric acid (CA) was the major detected organic acid by HPLC. In vitro, CA of T.asperellum at 75% completely repressed the growth of Fusariumoxysporum f. sp. lycopersici (FOL). In vivo, soaking tomato seeds in CA enhanced the seed germination and vigor index. T. asperellum and/or its CA suppressed the wilt disease caused by FOL compared to control. There was a proportional increment of plant growth and yield, as well as improvements in the biochemical parameters (chlorophyll pigments, total phenolic contents and peroxidase, and polyphenol oxidase activities), suggesting targeting both the bioconversion of MS into CA and biological control of FOL.

Bacillus velezensis manifests robust biocontrol activity against fungal plant pathogens, however, its antiviral activity has rarely been investigated. Bacillus velezensis strain PEA1 was isolated, characterized, and evaluated for antifungal and antiviral activities against Fusarium oxysporum MT270445 and cucumber mosaic virus (CMV) MN594112. Our findings proved that strain PEA1 had intense antagonist activity against F.oxysporum. Under greenhouse conditions, the antiviral activities (protective, curative, and inactivation) of PEA1-culture filtrate (CF) on Datura stramonium plants were assayed, using a half-leaf method. The inactivation treatment exhibited the highest inhibition rate (97.56%) and the most considerable reduction of CMV-CP accumulation levels (2.1-fold) in PEA1-CF-treated plants when compared with untreated plants (26.9-fold). Furthermore, PEA1-CF induced systemic resistance with significantly elevated transcriptional levels of PAL, CHS, HQT, PR-1, and POD genes in D. stramonium leaves after all treatments. Gas chromatography‒mass spectrometry analysis showed that pyrrolo[1,2-a]pyrazine-1,4-dione is the main compound in the PEA1-CF ethyl acetate extract, which may act as an elicitor molecule that induces plant systemic resistance and inhibits both fungal growth and viral replication. Consequently, B. velezensis can be considered as a potential source for the production of bioactive compounds for the management of plant diseases. To our knowledge, this is the first report of the antiviral activity of B. velezensis against plant viral infection.

This research aims to explore the effects of nanoparticles such as alumina (Al2O3) on the physical and mechanical properties of medium density fiberboards (MDF). The nanoparticles are added in urea-formaldehyde (UF) resin with different concentration levels e.g., 1.5%, 3%, and 4.5% by weight. A combination of forest fibers such as Populus Deltuidess (Poplar) and Euamericana (Ghaz) are used as a composite reinforcement due to their exceptional abrasion confrontation as well as their affordability and economic value with Al2O3-UF as a matrix or nanofillers for making the desired nanocomposite specimens. Thermo-gravimetric analysis (TGA) and thermal analytical analysis (TAA) in the form of differential scanning calorimetry (DSC) are carried out and it has been found that increasing the percentage of alumina nanoparticles leads to an increase in the total heat content. The mechanical properties such as internal bonding (IB), modulus of elasticity (MOE) and modulus of rupture (MOR), and physical properties such as density, water absorption (WA), and thickness swelling (TS) of the specimens have been investigated. The experimental results showed that properties of the new Nano-MDF are higher when compared to the normal samples. The results also showed that increasing the concentration of alumina nanoparticles in the urea-formaldehyde resin effects the mechanical properties of panels considerably.

Novel one-pot multicomponent synthesis of 2-pyrimidinamine derivatives can be achieved via green chemistry, using Cu(II)-tyrosinase enzyme (Cu-Tyr) as a catalyst. This method offers mild reaction conditions and a high yield of derivatives. We synthesised several compounds in this manner and evaluated their larvicidal, and antifeedant activities. Out of the synthesised derivatives, compound 3, with a median lethal dose (LD50) of 21.43 µg/mL, was highly active against Culex quinquefasciatus, compared to compounds 1a–m and 2, and the control, hydantocidin. Compounds 1j, 1d, and 1e were low active against C. quinquefasciatus with LD50 values of 78.46, 78.59, and 79.54 µg/mL, respectively. In antifeedant screening, compounds 1j, 1l, and 2 generated 100% mortality within 24 h against Oreochromis mossambicus at 100 µg/mL, where toxicity was determined as the ratio of the number of dead and live fingerlings (%) at 24 h. In contrast, compounds 1a–f, 1i, 1m, and 3 were less toxic to O. mossambicus as compared to the control, dibromoisophakellin. Therefore, compound 3 had high larvicidal activity against C. quinquefasciatus and was less toxic to non-target aquatic species. Molecular docking studies also supported the finding that compound 3 was an effective larvicide with more inhibition ability than the control hydantocidin (−9.6 vs. −6.1 kcal/mol).

The Batchwa vacha, Eutropiichthys vacha is commercially important, supporting a viable small- and large-scale fishery throughout the Ganges River, NW Bangladesh. This study provides detail information on reproduction of E. vacha including size at sexual maturity, spawning and peak spawning season, and fecundity based on 734 female specimens through regular monthly sampling using cast net, gill net, and square lift net in the Ganges River during January to December 2016. Also, our study estimated the effects of climate change including temperature and rainfall on reproduction of E. vacha in the Ganges River. For each individual, lengths (total length, TL; standard length, SL) and body weight (BW) were measured with slide caliper and digital balance, respectively. Gonads (ovaries) were collected carefully by ventral dissection of each female specimen and weighed to the nearest 0.01 g accuracy. The gonadosomatic index (GSI % = (GW/BW) ×100), modified gonadosomatic index (MGSI % = (GW/BW − GW) × 100), and Dobriyal index (DI = $$ \sqrt[3]{\mathrm{GW}} $$ ) were calculated to estimate the size at sexual maturity (L50) and spawning season. Based on GSI, MGSI, and DI, the L50 was calculated as 12.5 cm TL for female. The TL50, the TL at which 50% of individuals become mature, was calculated by logistic equation as 12.7 cm. Also, on the basis of higher values of GSI, MGSI, and DI, spawning season was ranged from April to August, with the peak in June–July, signifying the peak spawning season for E. vacha in the Ganges River. The total fecundity (FT) ranged from 4800 to 77,976 (mean ± SD, 31384 ± 23,747) and was highly correlated with TL and BW. Water temperature during the spawning period ranged from 28 to 34 °C, with an average of 31 °C and there was significant correlation between temperature and GSI. Also, the spawning season coincides with the peak rainfall and there was significant correlation between rainfall and GSI. Additionally, analysis of long data series indicated that annual average air temperature is increasing by 0.0258 °C/year, while the annual average rainfall is decreasing by 3.107 mm/year. Finally, the findings of this study would be very effective to impose specific management for E. vacha in the Ganges River and surrounding ecosystems.

A series of benzopyran-connected pyrimidine (1a–g) and benzopyran-connected pyrazole (2a–i) derivatives were synthesized via Biginelli reaction using a green chemistry approach. Cu(II)-tyrosinase was used as a catalyst in the synthesis of compounds 1a–g and 2a–i via the Biginelli reaction. The as-synthesized compounds were characterized by IR, 1H NMR, 13C NMR, mass spectroscopy, and elemental analysis. The as-synthesized compounds were screened for larvicidal and antifeedant activities. The larvicidal activity was evaluated using the mosquito species Culex quinquefasciatus, and the antifeedant activity was evaluated using the fishes of Oreochromis mossambicus. The compounds 2a–i demonstrated lethal effects, killing 50% of second instar mosquito larvae when their LD50 values were 44.17, 34.96, 45.29, 45.28, 75.96, and 28.99 μg mL−1, respectively. Molecular docking studies were used for analysis based on the binding ability of an odorant binding protein (OBP) of Culex quinquefasciatus with compound 2h (binding energy = −6.12 kcal mol−1) and compound 1g (binding energy = −5.79 kcal mol−1). Therefore, the proposed target compounds were synthesized via a green method using Cu(II)-enzyme as a catalyst to give high yield (94%). In biological screening, benzopyran-connected pyrazole (2h) was highly active compared with benzopyran-connected pyrimidine (1a–g) series in terms of larivicidal activity.

Two molecularly identified tomato isolates, Trichoderma asperelloides Ta41 and Rhizoctonia solani Rs33, were characterized and antagonistically evaluated. The dual culture technique showed that Ta41 had a high antagonistic activity of 83.33%, while a light microscope bioassay demonstrated that the Ta41 isolate over-parasitized the pathogen completely. Under greenhouse conditions, the application of Ta41 was able to promote tomato plant growth and had a significant increase in plant height, root length, and shoot fresh, shoot dry, root fresh, and root dry weight. It also improved chlorophyll content and total phenol content significantly, both in protective and in curative treatments. The protective treatment assay exhibited the lowest disease index (16.00%), while the curative treatment showed a disease index of 33.33%. At 20 days post-inoculation, significant increases in the relative expression levels of four defense-related genes (PR-1, PR-2, PR-3, and CHS) were observed in all Ta41-treated plants when compared with the non-treated plants. Interestingly, the plants treated with Ta41 alone showed the highest expression, with relative transcriptional levels of CHS, PR-3, PR-1, and PR-2 that were, compared with the control, 3.91-, 3.13-, 2.94-, and 2.69-fold higher, respectively, and the protective treatment showed relative transcriptional levels that were 3.50-, 3.63-, 2.39-, and 2.27-fold higher, respectively. Consequently, the ability of Ta41 to promote tomato growth, suppress Rs33 growth, and induce systemic resistance supports the incorporation of Ta41 as a potential bioagent for controlling root rot disease and increasing the productivity of crops, including tomatoes.

The Sclerotium tuber rot fungus (Sclerotium rolfsii Sacc.) represents a serious problem for Jerusalem artichoke (JA) tubers during storage periods. The aim of this study was to investigate an alternative preservation method using a natural essential oil to inhibit the fungal growth, increase storability, and keep nutritive value of JA tubers under storage conditions. In vitro antifungal activity was assessed using two essential oils; caraway and spearmint at concentrations of 2, 3, 4 and 5 %. Among the tested treatments, caraway oil at 2 % resulted in complete inhibition of the fungal growth. In the storage experiment, two preservation methods were applied using caraway oil. In the first method, JA tubers were treated with caraway oil at 2 %, kept in perforated polyethylene bags and stored at 4 °C and 90 % relative humidity (RH). In the second method, JA tubers were treated with caraway oil at 2 %, kept between peat moss layers and stored at room temperature (25/10 °C, day /night) and 70 % RH. Comparing with the infected-untreated control, tubers infected with S. rolfsii and treated with caraway oil which kept in peat moss exhibited lower severity of Sclerotium tuber rot, sprouting percentage and weight loss. On the other hand, this treatment led to the highest dry matter and contents of carbohydrates, protein, inulin and total phenols as well as the activity of peroxidase and polyphenol oxidase enzymes. Based on the obtained results we recommend the use of caraway oil and peat moss when storing JA tubers at room temperature due to its eco-safety and saving of the cooling energy.

During preservation, Jerusalem artichoke (JA) tubers are subjected to deterioration by mold fungi under storage, which signifies a serious problem. A new blue mold (Penicillium polonium) was recorded for the first time on JA tubers. Penicillium mold was isolated, identified (morphologically, and molecularly), and deposited in GenBank, (MW041259). The fungus has a multi-lytic capacity, facilitated by various enzymes capable of severely destroying the tuber components. An economic oil-based procedure was applied for preserving and retaining the nutritive value of JA tubers under storage conditions. Caraway and clove essential oils, at a concentration of 2%, were selected based on their strong antifungal actions. JA tubers were treated with individual oils under storage, kept between peat moss layers, and stored at room temperature. Tubers treated with both oils exhibited lower blue mold severity, sprouting and weight loss, and higher levels of carbohydrates, inulin, and protein contents accompanied by increased levels of defense-related phytochemicals (total phenols, peroxidase, and polyphenol oxidase). Caraway was superior, but the results endorse the use of both essential oils for the preservation of JA tubers at room temperature, as an economic and eco-safe storage technique against the new blue mold.

Globally, plant viral infection is one of the most difficult challenges of food security, where considerable losses in crop production occur. Nanoparticles are an effective control agent against numerous plant pathogens. However, there is limited knowledge concerning their effects against viral infection. In the present study, the green synthesis of zinc oxide nanoparticles (ZnO NPs) using aqueous leaf extract of Mentha spicata was achieved. X-ray diffraction patterns confirmed the crystalline nature of the prepared ZnO NPs. Dynamic light scattering and scanning electron microscopy analyses revealed that the resultant ZnO NPs were spherical in shape with a particle size ranged from 11 to 88 nm. Fourier transmission infrared spectroscopy detected different functional groups, capping and stability agents, and showed Zn-O bond within wavenumber of 487 cm&minus, 1. Under greenhouse conditions, the antiviral activity of biological synthesized ZnO NPs (100 &micro, g/mL) against Tobacco mosaic virus (TMV) was evaluated. The double foliar application of the prepared ZnO NPs, 24 h before and 24 h after TMV-inoculation, was the most effective treatment that showed a 90.21% reduction of viral accumulation level and disease severity. Additionally, the transcriptional levels of PAL, PR-1 (salicylic acid marker gene), CHS, and POD genes were induced and up-regulated in all ZnO NPs treated plants. Notably, the results exhibited that aqueous extract of Mentha spicata was an effective reducing agent for the green synthesis of ZnO NPs, which showed significant antiviral activity. Finally, the detected protective and curative activity of ZnO NPs against TMV can encourage us to recommend its application for plant viral disease management. To our knowledge, this is the first study describing the antiviral activity of the green synthesized ZnO NPs.

Alfalfa mosaic virus (AMV) causes significant losses in the global agricultural production of crops such as potato (Solanum tuberosum L.). Transcriptional levels of 10 innate defense genes, five related to the polyphenol biosynthetic pathway (PAL, HQT, HCT, CHS, and CHI) and five pathogenesis-related proteins (PR-1, PR-2, PR-3, PR-5 and PR-7) were investigated at different days post-inoculation (dpi). The results revealed that fluctuations in the expression of these examined defense genes between induction and suppression, especially in the first 10 dpi, are common. Interestingly, greater up-regulation of most of the tested genes at 4 dpi was associated with greater down-regulation of PR-2 and a reduction in viral coat protein (CP) accumulation. Conversely, greater activation and accumulation of the virus at 10 dpi suppressed the expressions of all genes except PR-1 (salicylic marker gene), and CHI genes showed 1.189- and 1.028-fold changes respectively. At 30 dpi, the greatest level of AMV-CP accumulation (42.27-fold) was associated with severe symptoms that started appearing at 18 dpi. Consequently, at 30 dpi, none of these genes had an effect on the presence and multiplication of the virus inside the plant cell. This study provides the first valuable information of the molecular transcriptional levels of these potato genes under AMV infection.

Prevention of food spoilage and food poisoning pathogens is usually achieved by use of chemical preservatives which have negative impacts including: human health hazards of the chemical applications, chemical residues in food & feed chains and acquisition of microbial resistance to the used chemicals. Because of such concerns, the necessity to find a potentially effective, healthy safer and natural alternative preservatives is increased. Within these texts, Plant extracts have been used to control food poisoning diseases and preserve foodstuff. Antimicrobial activity of five plant extracts were investigated against Bacillus cereus, Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa and Salmonella typhi using agar disc diffusion technique. Ethanolic extracts of Punica granatum, Syzygium aromaticum, Zingiber officinales and Thymus vulgaris were potentially effective with variable efficiency against the tested bacterial strains at concentration of 10 mg/ml while extract of Cuminum cyminum was only effective against S. aureus respectively. P. granatum and S. aromaticum ethanolic extracts were the most effective plant extracts and showed bacteriostatic and bactericidal activities against the highly susceptible strains of food borne pathogenic bacteria (S. aureus and P. aeruginosa) with MIC's ranged from 2.5 to 5.0 mg/ml and MBC of 5.0 and 10 mg/ml except P. aeruginosa which was less sensitive and its MBC reached to 12.5 mg/ml of S. aromaticum respectively. These plant extracts which proved to be potentially effective can be used as natural alternative preventives to control food poisoning diseases and preserve food stuff avoiding healthy hazards of chemically antimicrobial agent applications.