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ORIGINAL ARTICLE
Year : 2022  |  Volume : 13  |  Issue : 1  |  Page : 7-10  

Inhibition of bacillus spores germination by cinnamon bark, fingerroot, and moringa leaves extract


Department of Biology Pharmacy, Faculty of Pharmacy, Padjadjaran University, West Java, Indonesia

Date of Submission25-Sep-2021
Date of Decision30-Sep-2021
Date of Acceptance09-Nov-2021
Date of Web Publication21-Jan-2022

Correspondence Address:
Dr. Sri Agung Fitri Kusuma
Komplek Permata Biru, 71D, West Java
Indonesia
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/japtr.japtr_286_21

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  Abstract 


This study was intended to discover the natural food preservatives by comparing the antibacterial effect of the ethanolic extract of cinnamon bark, finger root, and moringa leaves toward Bacillus cereus both the vegetative cells and spores. The antibacterial activities of the investigated extracts were assessed against cells using the agar diffusion method. Whereas the sporicidal test was performed by observing the colony growth, after various times of incubation (1, 3, and 5 h). The investigated extracts produced inhibition in a diameter ranging from 10.6 to 35.3 mm, and it can be classified that the extract of cinnamon bark was the most potent extract to inhibit the vegetative cells form, followed by fingerroot and the moringa leaves extract. Consistently, the ethanolic extract of cinnamon bark and fingerroot significantly yielded sporicidal activities higher than the moringa leaves extract. Both extracts exerted sporicidal activity within 1 h of contact time at the lowest test concentration of 5% w/v, whereas moringa leaves extract required a longer contact time (5 h) at higher concentration of 20% w/v. It can be concluded that cinnamon bark and fingerroot extract have great potential as effective food preservative candidates to inhibit the B. cereus growth than moringa leaves extract.

Keywords: Bacillus cereus, cinnamon bark, fingerroot, moringa leaves, spores, vegetative cells


How to cite this article:
Kusuma SA, Septyadi R, Sofian FF. Inhibition of bacillus spores germination by cinnamon bark, fingerroot, and moringa leaves extract. J Adv Pharm Technol Res 2022;13:7-10

How to cite this URL:
Kusuma SA, Septyadi R, Sofian FF. Inhibition of bacillus spores germination by cinnamon bark, fingerroot, and moringa leaves extract. J Adv Pharm Technol Res [serial online] 2022 [cited 2023 Mar 29];13:7-10. Available from: https://www.japtr.org/text.asp?2022/13/1/7/336209




  Introduction Top


Bacillus cereus is ever present distributed in the milieu and known as a high-potential bacteria that can poison food manufacturing processes, improper food storage, refrigeration of improperly cooked food and ready to eat products, especially dairy products with its prevalence ranging at 2%–52%.[1],[2],[3],[4],[5],[6] Therefore, everyone has a great potential to be infected by these bacteria. The Center for Disease Control website states that monitoring outbreaks of Bacillus-related food poisoning (not just B. cereus) from 1998 to 2015, there were 619 outbreaks, 7385 diseases, 14,681 hospitalization rate and 337 deaths.[7],[8],[9],[10] B. cereus food poisoning is increasingly being reported as a serious and potentially fatal on the gastrointestinal or nonintestinal tract by secreting several toxins which can damage the target tissue.[11] These bacteria produce diarrheal toxins when they growth in the small intestine.[12] The food contamination may show diarrhea symptom if cells or spores in high numbers are ingested or may cause emetic symptom if the preformed toxins are ingested.[6] Furthermore, this bacterium may infect the respiratory tract, eye, and cause lesion.[13],[14] From a clinical and a food industry standpoint, endospores are dangerous because of their resistance to environmental stress and sterilization methods due to their potential to be dormant and possess rigid structure.[15] Therefore, contamination of endospores into food is the main transmission route for B. cereus because endospores can exist anywhere.[16],[17],[18],[19] Sterilization in the high temperature is reported to be effective at killing spores in foodstuffs; however, it should also be considered that overheating can damage organoleptic qualities and nutritional contents.[20] Therefore, this study explored the alternative ways to kill B. cereus spores by utilizing edible herbs, such as: Cinnamon Bark, fingerroot, and moringa leaves based on their antibacterial chemical content.


  Materials and Methods Top


Materials

All herbs collected from Manoko plantations in Lembang, Indonesia, in the periode of November–December 2020 and authenticated by Faculty of Biology, Padjadjaran University, Indonesia. The tested bacteria used in this study were B. cereus 11,778 and the bacteria was grown in Mueller Hinton Agar media (MHA-Oxoid CM0337).

Extraction

The plant materials were dried, weighed, and powdered using a grinder. A 500 g of each powdered materials was placed into macerator and soaked in ethanol (70% V/V) for 72 h at room temperature. The extract then analyzed to detect the secondary metabolites contents.[21]

Antibacterial activity

The antibacterial activities of the extracts were assessed against B. cereus using the standard agar diffusion method.

Sporicidal activity test

A total of one Ose of B. cereus colonies was suspended in a 5 mL sterile MHB and incubated for 96 h at 37°C to induce the spore forming. The suspension of vegetative cell was lysed for 5 min using sonication then centrifuged (12,000 × g for 2 min, 4°C) to isolate spores.[22],[23] The collected spores were resuspended and rinsed using sterile distilled water by repeated centrifugation. The pellets containing spore were resuspended in sterile physiological saline solution and the condition of spore was observed by spore stain technique using carbol fuchsin ast the primer stain and methylene blue as the counter dye. The sporicidal activity of the extract was determined by observing the presence or absence of colony growth on agar media. Spore suspension (0.5 McFarland) was taken for 10 μL and challenged with 1 mL of each extract with various concentrations then incubated at 37°C for various times. The spores were isolated by centrifugation, following by pellets washing and resuspension in 1 mL of sterile saline solution. A 10 μL of spore suspension was spread on MHA and the viable spores were observed.


  Results and Discussion Top


A total of three crude ethanolic extracts was screened for the antibacterial potential against the vegetative cells form of B. cereus, presented in [Figure 1] and [Table 1]. In this present study, the investigated extracts possessed different secondary metabolite content, Cinnamomum bark contains of flavonoids, tannins, polyphenolics, monoterpenoids and sesquiterpenoids, and quinones; fingerroot contains of flavonoids, polyphenolics, quinones, monoterpenoids and sesquiterpenoids; moringa contains of flavonoids, tannins, polyphenolics, and quinones. Another study reported that flavonoids substance containing in Roselle extract was suggested to play a role as the antibacterial agent against B. cereus cells.[24] Flavonoids can form complexes with dissolved proteins that are located outside the bacterial cell and disturb the DNA synthesis.[25],[26],[27] The polyphenolics substances were also predicted to have an important role in the inhibition of investigating extracts against B. cereus. Several studies have depicted that the polyphenolic compounds can modify the cell membrane permeability.[26],[28],[29],[30], [31,[32],[33] Meanwhile, Quinones work by inactivate the bacterial protein by irreversibly binding to the bacterial amino acids.[34] The antibacterial activity demonstrated that the Cinnamon bark extract generated the highest antibacterial potential against the vegetative cells, followed by fingerroot extract. Meanwhile, the effectivity of moringa leaf extract was less effective. These results were in accordance with the secondary metabolite content of each extract. The differences in the types and concentrations of secondary metabolites are thought to yield a great effect on the inhibition potency of the extract against B. cereus cells.[35] The moringa leaves extract required a minimum concentration of 20%w/v to produce antibacterial activity against B. cereus cells. The sporicidal activities of the extracts are presented in [Table 2]. We revealed that the ethanolic extract of cinnamon bark and fingerroot significantly yielded sporicidal activities higher than the moringa leaves extract. Both extracts exerted sporicidal activity spores within 1 h at the lowest test concentration of 5% w/v, meanwhile moringa leaves extract required a longer contact time (5 h) at higher concentration of 20% w/v. The result showed that cinnamon bark and fingerroot extract have great potential as effective food preservative candidates to inhibit both forms of B. cereus. This is interesting because up to now, resistance cases of B. cereus spores against chemical substances and sporicidal enzymes have been identified, especially due to their integrity structure with triple layering of the spore (coat, protoplast membrane, and nucleus) and chemical composition to face the stressful environmental.[36],[37],[38] Meanwhile, for the spore integrity, the outer membrane is not an essential protective layer because its release was found not provide a significant effect on spore resistance.[36],[37] In contrast to the outer, the inner membrane is a vigorous permeability constraint, importantly maintains the inside structure of the spore, especially the DNA, and have resistance mechanisms towards the anti-sporicidal chemical substances.[36],[35],[36],[37],[38],[39],[40] We suggested that the investigated extracts can penetrate and made the inner membrane of the spore to be lysed, thus, the spore unable to germinate and grow on the media. These findings provide strong evidence that the content of secondary metabolites in the studied extracts was responsible for the antibacterial activity against B. cereus. By comparing the secondary metabolite content in others plant extracts, we suggested that our investigated extracts had the same opportunity as the sporicidal agent candidate of B. cereus's spore germination and outgrowth. As reported in another study, edible burdock root and olives extract that consist of flavonoid-types, terpenoids, several polyphenols and tannins, provided the sporicidal activity on B. cereus spores.[41],[42] Thus, this finding is interesting because spores have a complex structure and are not easily to be penetrated. Moreover, considering that plant extracts that are effective against B. cereus spores have been reported less than those of B. subtilis. In addition, as Lau and Rukayadi said, reports of studies of sporicidal activity derived from plants are still rare.[43] Therefore, scientific evidence of the ability of ethanol extract of cinnamon bark and fingerroot provides a great opportunity in overcoming the problem of resistance to B. cereus spores that have existed so far.
Figure 1: Antibacterial activity of cinnamon bark (a), Fingerroot (b) and Moringa leaves (c) ethanolic extract against vegetative cells of Bacillus cereus

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Table 1: Antibacterial activity of all tested ethanolic extract against Bacillus cereus cells vegetative

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Table 2: Sporicidal activities of the extracts

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  Conclusion Top


The present findings indicated that the ethanolic extract of cinnamon bark and fingerroot provided strong and significant antibacterial and sporicidal agents, compared to that of moringa leaves extract. Thus, cinnamon bark and fingerroot extracts might be potential to be further studied as a food preservative.

Acknowledgment

The research was supported and funded by Padjadjaran University.

Financial support and sponsorship

A grant from Padjadjaran University.

Conflicts of interest

There are no conflicts of interest.



 
  References Top

1.
Granum PE, Lund T. Mini review: Bacillus cereus and its food poisoning toxin. FEMS Microbiol Lett 1997;157:223-8.  Back to cited text no. 1
    
2.
Wijnands LM, Dufrenne JB, Rombouts FM, in 't Veld PH, van Leusden FM. Prevalence of potentially pathogenic Bacillus cereus in food commodities in the Netherlands. J Food Prot 2006;69:2587-94.  Back to cited text no. 2
    
3.
Wong HC, Chen YL, Chen CL. Growth, germination and toxigenic activity of Bacillus cereus in milk products. J Food Prot 1988;51:707-10.  Back to cited text no. 3
    
4.
Svensson B, Monthán A, Shaheen R, Andersson MA, Salkinoja M, Salonen A, et al. Occurrence of emetic toxin producing Bacillus cereus in the dairy production chain. Int Dairy J 2006;16:740-9.  Back to cited text no. 4
    
5.
Spanu C, Scarano C, Spanu V, Pala C, Casti D, Lamon S, et al. Occurrence and behavior of Bacillus cereus in naturally contaminated ricotta salata cheese during refrigerated storage. Food Microbiol 2016;58:135-8.  Back to cited text no. 5
    
6.
Schneider KR, Parish ME, Goodrich RM, Cookingham T. Preventing Foodborne Illness: Bacillus Cereus and Bacillus Anthracis. University of Florida: Florida; 2004.  Back to cited text no. 6
    
7.
Thein CC, Trinidad RM, Pavlin BI. A large foodborne outbreak on a small Pacific island. Pac Health Dialog 2010;16:75-80.  Back to cited text no. 7
    
8.
May FJ, Polkinghorne BG, Fearnley EJ. Epidemiology of bacterial toxin-mediated foodborne gastroenteritis outbreaks in Australia, 2001 to 2013. Commun Dis Intell Q Rep 2016;40:E460-9.  Back to cited text no. 8
    
9.
Kotiranta A, Haapasalo M, Kari K, Kerosuo E, Olsen I, Sorsa T, et al. Surface structure, hydrophobicity, phagocytosis, and adherence to matrix proteins of Bacillus cereus cells with and without the crystalline surface protein layer. Infect Immun 1998;66:4895-902.  Back to cited text no. 9
    
10.
European Food Safety Authority (EFSA). Risks for public health related to the presence of Bacillus cereus and other Bacillus spp. Including Bacillus thuringiensis in foodstuffs. EFSA J 2016;14:1-93.  Back to cited text no. 10
    
11.
Jovanovic J, Ornelis VF, Madder A, Rajkovic A. Bacillus cereus food intoxication and toxicoinfection. Compr Rev Food Sci Food Saf 2021;20:3719-61.  Back to cited text no. 11
    
12.
Ehling-Schulz M, Guinebretiere MH, Monthán A, Berge O, Fricker M, Svensson B. Toxin gene profiling of enterotoxic and emetic Bacillus cereus. FEMS Microbiol Lett 2006;260:232-40.  Back to cited text no. 12
    
13.
Nguyen AT, Tallent SM. Screening food for Bacillus cereus toxins using whole genome sequencing. Food Microbiol 2019;78:164-70.  Back to cited text no. 13
    
14.
Hölzel CS, Tetens JL, Schwaiger K. Unraveling the role of vegetables in spreading antimicrobial-resistant bacteria: A need for quantitative risk assessment. Foodborne Pathog Dis 2018;15:671-88.  Back to cited text no. 14
    
15.
Jenson I, Moir CJ. Bacillus cereus and other Bacillus species. In: Hocking AD, editor. Foodborne Microorganisms of Public Health Significance. 6th ed., Ch. 14. Sydney: Australian Institute of Food Science and Technology (NSW Branch); 2003.  Back to cited text no. 15
    
16.
Vilain S, Luo Y, Hildreth MB, Brözel VS. Analysis of the life cycle of the soil saprophyte Bacillus cereus in liquid soil extract and in soil. Appl Environ Microbiol 2006;72:4970-7.  Back to cited text no. 16
    
17.
Andersson A, Granum PE, Rönner U. The adhesion of Bacillus cereus spores to epithelial cells might be an additional virulence mechanism. Int J Food Microbiol 1998;39:93-9.  Back to cited text no. 17
    
18.
Rönner U, Husmark U, Henriksson A. Adhesion of Bacillus spores in relation to hydrophobicity. J Appl Bacteriol 1990;69:550-6.  Back to cited text no. 18
    
19.
Ubong A, New CY, Chai LC, Nur FA, Nur HK, Nishibuchi M, et al. Impact of temperature on Bacillus cereus spore germination in ultra-high temperature chocolate milk. Food Res 2019;3;808-13.  Back to cited text no. 19
    
20.
Cho WI, Chung MS. Antimicrobial effect of a combination of herb extract and organic acid against Bacillus subtilis spores. Food Sci Biotechnol 2017;26:1423-8.  Back to cited text no. 20
    
21.
Farnsworth NR, Akerele O, Bingel AS, Soejarto DD, Guo Z. Medicinal plants in therapy. Bull World Health Organ 1985;63:965-81.  Back to cited text no. 21
    
22.
Hamouda T, Shih AY, Baker JR Jr. A rapid staining technique for the detection of the initiation of germination of bacterial spores. Lett Appl Microbiol 2002;34:86-90.  Back to cited text no. 22
    
23.
Cho WI, Choi JB, Lee KP, Cho SC, Park EJ, Chung MS, et al. Antimicrobial activity of medicinal plants against Bacillus subtilis spore. Food Sci Biotechnol 2007;16:1072-7.  Back to cited text no. 23
    
24.
Elmanama AA, Alyazji AA, Abu-Gheneima N. Antibacterial, antifungal and synergistic effect of Lawsonia inermis, Punica granatum and Hibiscus sabdariffa. Ann Alquds Med 2011;7:33-41.  Back to cited text no. 24
    
25.
Tsuchiya H, Sato M, Miyazaki T, Fujiwara S, Tanigaki S, Ohyama M, et al. Comparative study on the antibacterial activity of phytochemical flavanones against methicillin-resistant Staphylococcus aureus. J Ethnopharmacol 1996;50:27-34.  Back to cited text no. 25
    
26.
Cushnie TP, Lamb AJ. Recent advances in understanding the antibacterial properties of flavonoids. Int J Antimicrob Agents 2011;38:99-107.  Back to cited text no. 26
    
27.
Haraguchi H, Tanimoto K, Tamura Y, Mizutani K, Kinoshita T. Mode of antibacterial action of retrochalcones from Glycyrrhiza inflata. Phytochemistry 1998;48:125-9.  Back to cited text no. 27
    
28.
Ikigai H, Nakae T, Hara Y, Shimamura T. Bactericidal catechins damage the lipid bilayer. Biochim Biophys Acta 1993;1147:132-6.  Back to cited text no. 28
    
29.
Stapleton PD, Shah S, Hamilton-Miller JM, Hara Y, Nagaoka Y, Kumagai A, et al. Anti-Staphylococcus aureus activity and oxacillin resistance modulating capacity of 3-O-acyl-catechins. Int J Antimicrob Agents 2004;24:374-80.  Back to cited text no. 29
    
30.
Taguri T, Tanaka T, Kouno I. Antibacterial spectrum of plant polyphenols and extracts depending upon hydroxyphenyl structure. Biol Pharm Bull 2006;29:2226-35.  Back to cited text no. 30
    
31.
Mason TL, Wasserman BP. Inactivation of red beet betaglucan synthase by native and oxidized phenolic compounds. Phytochem 1987;26:2197-202.  Back to cited text no. 31
    
32.
Sikkema J, de Bont JA, Poolman B. Mechanisms of membrane toxicity of hydrocarbons. Microbiol Rev 1995;59:201-22.  Back to cited text no. 32
    
33.
Fei P, Xu Y, Zhao S, Gong S, Guo L. Olive oil polyphenol extract inhibits vegetative cells of Bacillus cereus isolated from raw milk. J Dairy Sci 2019;102:3894-902.  Back to cited text no. 33
    
34.
Stern JL, Hagerman AE, Steinberg PD, Mason PK. Phlorotannin-protein interactions. J Chem Ecol 1996;22:1877-99.  Back to cited text no. 34
    
35.
Monks NR, Lerner C, Henriques AT, Farias RM, Schapoval EE, Suyenaga SS, et al. Anticancer, antichemotactic and antimicrobial activities of marine sponges collected off the coast of Santa Catarina, Southern Brazil. J Exp Mar Biol Ecol 2002;281:1-12.  Back to cited text no. 35
    
36.
Setlow B, McGinnis KA, Ragkousi K, Setlow P. Effects of major spore-specific DNA binding proteins on Bacillus subtilis sporulation and spore properties. J Bacteriol 2000;182:6906-12.  Back to cited text no. 36
    
37.
Nicholson WL, Munakata N, Horneck G, Melosh HJ, Setlow P. Resistance of Bacillus endospores to extreme terrestrial and extraterrestrial environments. Microbiol Mol Biol Rev 2000;64:548-72.  Back to cited text no. 37
    
38.
Russell AD. Bacterial spores and chemical sporicidal agents. Clin Microbiol Rev 1990;3:99-119.  Back to cited text no. 38
    
39.
Driks A. Bacillus subtilis spore coat. Microbiol Mol Biol Rev 1999;63:1-20.  Back to cited text no. 39
    
40.
Cortezzo DE, Setlow P. Analysis of factors that influence the sensitivity of spores of Bacillus subtilis to DNA damaging chemicals. J Appl Microbiol 2005;98:606-17.  Back to cited text no. 40
    
41.
Dabiri A, Karbasizade V. Evaluation of the sporicidal activity of ethanol extract of Arctium lappa root against Bacillus cereus. Zahedan J Res Med Sci 2014;16:47-9.  Back to cited text no. 41
    
42.
Tassou CC, Nychas GJ, Board RG. Effect of phenolic compounds and oleuropein on the germination of Bacillus cereus T spores. Biotechnol Appl Biochem 1991;13:231-7.  Back to cited text no. 42
    
43.
Lau KY, Rukayadi Y. Screening of tropical medicinal plants for sporicidal activity. Int Food Res J 2015;22:415-9.  Back to cited text no. 43
    


    Figures

  [Figure 1]
 
 
    Tables

  [Table 1], [Table 2]



 

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