scholarly journals Phytochemical constituents and antibacterial activities of indigenous chewing stick (Anogeissus leiocarpus) stem

2021 ◽  
Vol 14 (1) ◽  
pp. 85-94
Author(s):  
M.M. Namadina ◽  
A.U. Mukhtar ◽  
S.I. Karaye ◽  
F.M. Musa ◽  
I.H. Bah ◽  
...  

The stems from Anogeissus leiocarpus are commonly used as chewing sticks in Northern Nigeria. If properly used, the chewing sticks have proven to be effective in removing dental plaque due to mechanical cleaning and enhanced salivation. Chewing sticks from other plants have been shown to display antimicrobial activities against a broad spectrum of microorganisms. However, there is limited information available in Northern Nigeria on the chemical composition, antimicrobial properties and the ability of the plants under study to prevent bacterial adhesion to tooth surface. Therefore, the purpose of this study was to ascertain the phytochemical and antibacterial properties of Anogeissus leiocarpus and correlate the results obtained to their ethnomedicinal uses as chewing sticks. Powdered stem was exhaustively extracted using methanol at room temperature for 72 hours. Antibacterial activities of the methanol extract was assessed using the agar well diffusion methods against the oral pathogens, Staphylococcus aureus, Streptococcus salivarius, Streptococcus pyogenes, Streptococcus mutans and Streptococcus sanguinis. Acute toxicity study was achieved using Lorke method. Phytochemicals which include flavonoid, steroid, triterpenes, alkaloids, tannins, carbohydrate, glycoside, phenols were detected in the extracts while anthraquinones was absent. The antibacterial results revealed that, the methanol extract had promising antibacterial activity. S. aureuswas found to be the most susceptible bacteria at 500mg/ml with inhibition of 22 mm, Streptococcus salivarius, Streptococcus pyogenes and Streptococcus sanguinis were inhibited at 16 mm while Streptococcus mutans showed inhibition of 14 mm. The extract have MIC and MBC of 31.25 mg/ml and 62.5 mg/ml respectively against all the tested clinical isolates. The LD50 of Anogeissus leiocarpus was found to be greater than 5000 mg/kg and could be considered safe for consumption.

2021 ◽  
Vol 10 (1) ◽  
pp. e39310111539
Author(s):  
Thais Oliveira Cordeiro ◽  
Angélica Kercya Pereira de Mendonça ◽  
Mayra Sousa Gomes ◽  
Emanuelle Louyde Ferreira de Lima ◽  
Maria Regina Macedo Costa ◽  
...  

Objetivo: O objetivo do presente estudo foi avaliar in vitro a atividade antimicrobiana do extrato hidroetanólico da folha de Spondias mombin (S. mombin L.) sobre bactérias do gênero Streptococcus: S. mutans, S. mitis, S. oralis, S. sanguinis e S. salivarius, comparando-a à atividade antimicrobiana da solução de digluconato de clorexidina 0,12% sobre essas mesmas bactérias. Metodologia: Foram realizados os testes in vitro de Determinação da Concentração Inibitória Mínima, Determinação da Concentração Inibitória Mínima de Aderência e Análise da Cinética Bactericida. Resultados: Para o Streptococcus mutans, o grupo controle foi estatisticamente superior (p<0,05) ao extrato até a concentração 31,25mg/ml, não ocorrendo diferença estatística nas demais concentrações. Para o Streptococcus oralis, o extrato foi estatisticamente superior (p<0,05) ao grupo controle em sua forma bruta (500mg/ml), o grupo controle teve significância estatística (p<0,05) sobre o extrato apenas nas concentrações 62,5mg/ml, 31,25mg/ml, 1,95mg/ml e 0,97mg/ml. Para o Streptococcus sanguinis, foi constatado que o extrato foi estatisticamente superior (p<0,05) ao grupo controle nas duas primeiras concentrações 500mg/ml e 250mg/ml, ao passo que o grupo controle teve significância estatística (p<0,05) sobre o extrato apenas nas duas últimas concentrações: 1,95mg/ml e 0,97mg/ml. O grupo controle foi estatisticamente superior (p<0,05) ao extrato em todas as concentrações no Streptococcus mitis, exceto para a concentração 31,25mg/ml. Para a Streptococcus salivarius, o extrato foi estatisticamente superior (p<0,05) ao grupo controle na maioria das concentrações testadas, com exceção apenas para 15,65mg/ml e 1,95mg/ml, que não foram observados diferenças estatisticamente significativas entre o extrato e o grupo controle. Conclusão: o extrato hidroetanólico de Spondias mombin L., em diferentes concentrações, apresenta atividade antimicrobiana semelhante ao digluconato de clorexidina a 0,12% frente a bactérias bucais do gênero Streptococcus.


2018 ◽  
Vol 15 (8) ◽  
pp. 843-850
Author(s):  
Malgorzata Miazga-Karska ◽  
Maciej Wos ◽  
Agnieszka A. Kaczor ◽  
Anna Pachuta-Stec ◽  
Grazyna Ginalska ◽  
...  

2021 ◽  
Vol 11 (7) ◽  
pp. 3232
Author(s):  
Jingyang Zhang ◽  
Sofiya-Roksolana Got ◽  
Iris Xiaoxue Yin ◽  
Edward Chin-Man Lo ◽  
Chun-Hung Chu

Studies have shown that silver diamine fluoride (SDF) is an effective agent to arrest and prevent dental caries due to its mineralizing and antibacterial properties. While plenty of studies have investigated the mineralizing properties, there are few papers that have examined its antibacterial effect on oral biofilm. The objective of this study was to identify the effect of silver diamine fluoride on oral biofilm. Method: The keywords used were (silver diamine fluoride OR silver diammine fluoride OR SDF OR silver fluoride OR AgF AND biofilm OR plaque). Two reviewers screened the titles and abstracts and then retrieved the full text of the potentially eligible publications. Publications of original research investigating the effect of SDF on oral biofilm were selected for this review. Results: This review included 15 laboratory studies and six clinical studies among the 540 papers identified. The laboratory studies found that SDF could prevent bacterial adhesion to the tooth surface. SDF also inhibited the growth of cariogenic bacteria, including Streptococcus mutans, Lactobacillus acidophilus, Streptococcus sobrinus, Lactobacillus rhamnosus, Actinomyces naeslundii, and Enterococcus faecalis, thus contributing to its success in caries arrest. One clinical study reported a decrease in Streptococcus mutans and Lactobacillus sp. in arrested caries after SDF treatment, and another clinical study found that SDF inhibited the growth of periodontitis microbiota, including Porphyromonas gingivalis, Tannerella forsythia, and Prevotella intermedia/nigrescens. However, three clinical studies reported no significant change in the microbial diversity of the plaque on the tooth after SDF treatment. Moreover, one laboratory study and one clinical research study reported that SDF inhibited the growth of Candida albicans. Conclusion: Not many research studies have investigated the effects of SDF on oral biofilm, although SDF has been used as a caries-arresting agent with antibacterial properties. However, a few publications have reported that SDF prevented bacterial adhesion to the teeth, inhibited the growth of cariogenic and periodontal bacteria, and possessed antifungal properties.


2013 ◽  
Vol 80 (1) ◽  
pp. 97-103 ◽  
Author(s):  
Dan Li ◽  
Yukie Shibata ◽  
Toru Takeshita ◽  
Yoshihisa Yamashita

ABSTRACTAStreptococcus mutansmutant defective in aciduricity was constructed by random-insertion mutagenesis. Sequence analysis of the mutant revealed a mutation ingidA, which is known to be involved in tRNA modification inStreptococcus pyogenes. Complementation ofgidAbyS. pyogenesgidArecovered the acid tolerance ofS. mutans. Although thegidA-inactivatedS. pyogenesmutant exhibited significantly reduced expression of multiple extracellular virulence proteins, theS. mutansmutant did not. On the other hand, thegidAmutant ofS. mutansshowed reduced ability to withstand exposure to other stress conditions (high osmotic pressure, high temperature, and bacitracin stress) besides an acidic environment. In addition, loss of GidA decreased the capacity for glucose-dependent biofilm formation by over 50%. This study revealed thatgidAplays critical roles in the survival ofS. mutansunder stress conditions, including lower pH.


2013 ◽  
Vol 15 (1) ◽  
pp. 41-46 ◽  
Author(s):  
A.C.L. Albuquerque ◽  
M.S.V. Pereira ◽  
D.F. Silva ◽  
L.F. Pereira ◽  
F.A.C. Viana ◽  
...  

Most illnesses affecting the oral cavity are proven to have infectious origin. Several categories of chemical agents have been used in the chemical control of dental biofilm through strategies that aim at reducing bacterial adhesion and inhibiting the growth and the proliferation of microorganisms on the tooth surface. The use of plants in folk medicine and in Dentistry, as well as the spread of successful cases, has led to scientific exploration, resulting in chemical-pharmacological knowledge of thousands of plants. The present study aimed to evaluate the anti-adherence activity of Lippia sidoides Cham., comparing the results with those of 0.12% chlorhexidine by means of an in vitro simulation of dental biofilm. The studied bacterial strains were Streptococcus mutans, Streptococcus sanguinis and Lactobacillus casei, main responsible for the biofilm adherence. The studied extract was effective in inhibiting the adherence of Streptococcus mutans up to a concentration of 1:16, compared to Chlorhexidine. Lippia sidoides Cham extract showed anti-adherence effect on the major microorganisms responsible for dental biofilm consolidation.


2018 ◽  
Vol 201 (2) ◽  
Author(s):  
Lin Zeng ◽  
Robert A. Burne

ABSTRACTThe dental caries pathogenStreptococcus mutanscan ferment a variety of sugars to produce organic acids. Exposure ofS. mutansto certain nonmetabolizable carbohydrates, such as xylitol, impairs growth and can cause cell death. Recently, the presence of a sugar-phosphate stress inS. mutanswas demonstrated using a mutant lacking 1-phosphofructokinase (FruK) that accumulates fructose-1-phosphate (F-1-P). Here, we studied an operon inS. mutans,sppRA, which was highly expressed in thefruKmutant. Biochemical characterization of a recombinant SppA protein indicated that it possessed hexose-phosphate phosphohydrolase activity, with preferences for F-1-P and, to a lesser degree, fructose-6-phosphate (F-6-P). SppA activity was stimulated by Mg2+and Mn2+but inhibited by NaF. SppR, a DeoR family regulator, repressed the expression of thesppRAoperon to minimum levels in the absence of the fructose-derived metabolite F-1-P and likely also F-6-P. The accumulation of F-1-P, as a result of growth on fructose, not only inducedsppAexpression, but it significantly altered biofilm maturation through increased cell lysis and enhanced extracellular DNA release. Constitutive expression ofsppA, via a plasmid or by deletingsppR, greatly alleviated fructose-induced stress in afruKmutant, enhanced resistance to xylitol, and reversed the effects of fructose on biofilm formation. Finally, by identifying three additional putative phosphatases that are capable of promoting sugar-phosphate tolerance, we show thatS. mutansis capable of mounting a sugar-phosphate stress response by modulating the levels of certain glycolytic intermediates, functions that are interconnected with the ability of the organism to manifest key virulence behaviors.IMPORTANCEStreptococcus mutansis a major etiologic agent for dental caries, primarily due to its ability to form biofilms on the tooth surface and to convert carbohydrates into organic acids. We have discovered a two-gene operon inS. mutansthat regulates fructose metabolism by controlling the levels of fructose-1-phosphate, a potential signaling compound that affects bacterial behaviors. With fructose becoming increasingly common and abundant in the human diet, we reveal the ways that fructose may alter bacterial development, stress tolerance, and microbial ecology in the oral cavity to promote oral diseases.


2010 ◽  
Vol 192 (12) ◽  
pp. 3024-3032 ◽  
Author(s):  
H. Koo ◽  
J. Xiao ◽  
M. I. Klein ◽  
J. G. Jeon

ABSTRACT Streptococcus mutans is a key contributor to the formation of the extracellular polysaccharide (EPS) matrix in dental biofilms. The exopolysaccharides, which are mostly glucans synthesized by streptococcal glucosyltransferases (Gtfs), provide binding sites that promote accumulation of microorganisms on the tooth surface and further establishment of pathogenic biofilms. This study explored (i) the role of S. mutans Gtfs in the development of the EPS matrix and microcolonies in biofilms, (ii) the influence of exopolysaccharides on formation of microcolonies, and (iii) establishment of S. mutans in a multispecies biofilm in vitro using a novel fluorescence labeling technique. Our data show that the ability of S. mutans strains defective in the gtfB gene or the gtfB and gtfC genes to form microcolonies on saliva-coated hydroxyapatite surfaces was markedly disrupted. However, deletion of both gtfB (associated with insoluble glucan synthesis) and gtfC (associated with insoluble and soluble glucan synthesis) is required for the maximum reduction in EPS matrix and biofilm formation. S. mutans grown with sucrose in the presence of Streptococcus oralis and Actinomyces naeslundii steadily formed exopolysaccharides, which allowed the initial clustering of bacterial cells and further development into highly structured microcolonies. Concomitantly, S. mutans became the major species in the mature biofilm. Neither the EPS matrix nor microcolonies were formed in the presence of glucose in the multispecies biofilm. Our data show that GtfB and GtfC are essential for establishment of the EPS matrix, but GtfB appears to be responsible for formation of microcolonies by S. mutans; these Gtf-mediated processes may enhance the competitiveness of S. mutans in the multispecies environment in biofilms on tooth surfaces.


2021 ◽  
Vol 9 (11) ◽  
pp. 2308
Author(s):  
Yusuke Iwabuchi ◽  
Tomoyo Nakamura ◽  
Yasuka Kusumoto ◽  
Ryoma Nakao ◽  
Tsutomu Iwamoto ◽  
...  

Streptococcus mutans releases membrane vesicles (MVs) and induces MV-dependent biofilm formation. Glucosyltransferases (Gtfs) are bound to MVs and contribute to the adhesion and glucans-dependent biofilm formation of early adherent bacteria on the tooth surface. The biofilm formation of S. mutans may be controlled depending on whether the initial pH tends to be acidic or alkaline. In this study, the characteristics and effects of MVs extracted from various conditions {(initial pH 6.0 and 8.0 media prepared with lactic acid (LA) and acetic acid (AA), and with NaOH (NO), respectively)} on the biofilm formation of S. mutans and early adherent bacteria were investigated. The quantitative changes in glucans between primary pH 6.0 and 8.0 conditions were observed, associated with different activities affecting MV-dependent biofilm formation. The decreased amount of Gtfs on MVs under the initial pH 6.0 conditions strongly guided low levels of MV-dependent biofilm formation. However, in the initial pH 6.0 and 8.0 solutions prepared with AA and NO, the MVs in the biofilm appeared to be formed by the expression of glucans and/or extracellular DNA. These results suggest that the environmental pH conditions established by acid and alkaline factors determine the differences in the local pathogenic activities of biofilm development in the oral cavity.


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