Chemical characterization, antibacterial and antifungal activity of honey pots and pollen pots obtained from the stingless bee Tetragonisca angustula (Latreille, 1811)

IF 3.5 3区 医学 Q2 FOOD SCIENCE & TECHNOLOGY Food and Chemical Toxicology Pub Date : 2025-03-01 Epub Date: 2025-02-02 DOI:10.1016/j.fct.2025.115305
Nair Silva Macêdo , Zildene de Sousa Silveira , Débora Menezes Dantas , Cristina Rodrigues dos Santos Barbosa , Antonia Thassya Lucas dos Santos , Thiago Araújo de Medeiros Brito , Josean Fechine Tavares , Débora Odília Duarte Leite , Priscilla Ramos Freitas Alexandre , José Galberto Martins da Costa , Cícera Datiane de Morais Oliveira-Tintino , Henrique Douglas Melo Coutinho , Maria Flaviana Bezerra Morais-Braga , Francisco Assis Bezerra da Cunha
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Abstract

This study aimed to determine the chemical composition of the ethanolic extracts of honey pots (EEHPTa) and pollen pots (EEPPTa) from the stingless bee Tetragonisca angustula, as well as to evaluate their antimicrobial activity against Staphylococcus aureus, Pseudomonas aeruginosa, Escherichia coli, Candida albicans, and Candida tropicalis. The chemical composition was determined using HPLC-Q-TOF-MS/MS and HPLC-DAD, while antimicrobial assays were performed using the broth microdilution method. Eleven compounds were identified in EEHPTa and nine in EEPPTa, including cirsimaritin, 3ʹ-prenylnaringenin, xanthohumol, lespedezaflavanone B, and 19α-hydroxyursolic acid. The extracts enhanced the action of norfloxacin against S. aureus (MIC reduced from 256 to 128 μg/mL). With gentamicin, EEHPTa reduced the MIC from 17.95 to 11.31 μg/mL, while EEPPTa reduced it to 12.69 μg/mL. Only EEHPTa was effective with ampicillin, reducing the MIC from 71.83 to 31.7 μg/mL. Against P. aeruginosa, EEHPTa decreased the MIC of gentamicin from 8 to 4 μg/mL, whereas EEPPTa exhibited an antagonistic effect. For E. coli, only EEPPTa reduced the MIC from 64 to 57.01 μg/mL. EEHPTa exhibited lower IC50 values against yeast (C. albicans: 65.47 μg/mL; C. tropicalis: 29.79 μg/mL) compared to EEPPTa (C. albicans: 820.7 μg/mL; C. tropicalis: 809.9 μg/mL). Both extracts enhanced the effect of fluconazole against C. albicans but showed no effect on the C. tropicalis strain. These findings highlight the therapeutic potential of the secondary metabolites in these extracts, reinforcing their importance in the development of new antimicrobial and antifungal strategies.
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从无刺蜜蜂Tetragonisca angustula中提取的蜂蜜罐和花粉罐的化学特性、抗菌和抗真菌活性(Latreille, 1811)。
本研究旨在测定无刺蜜蜂蜂蜜罐(EEHPTa)和花粉罐(EEPPTa)乙醇提取物的化学成分,并评价其对金黄色葡萄球菌、铜绿假单胞菌、大肠杆菌、白色念珠菌和热带念珠菌的抑菌活性。采用HPLC-Q-TOF-MS/MS和HPLC-DAD测定化学成分,采用肉汤微量稀释法测定抗菌活性。在EEHPTa中鉴定出11个化合物,在EEPPTa中鉴定出9个化合物,包括茜草素、3′-烯丙基柚皮素、黄腐酚、胡子木黄酮B和19α-羟基熊果酸。该提取物增强了诺氟沙星对金黄色葡萄球菌的抑制作用(MIC由256 μg/mL降至128 μg/mL)。与庆大霉素相比,EEHPTa将MIC从17.95降低到11.31 μg/mL, EEPPTa将MIC降低到12.69 μg/mL。只有EEHPTa与氨苄西林有效,MIC从71.83降至31.7 μg/mL。对铜绿假单胞菌,EEHPTa能使庆大霉素的MIC从8 μg/mL降至4 μg/mL,而EEPPTa具有拮抗作用。对于大肠杆菌,只有EEPPTa能将MIC从64降低到57.01 μg/mL。EEHPTa对酵母菌的IC50值较低(白色念珠菌:65.47 μg/mL;热带念珠菌:29.79 μg/mL)与EEPPTa(白色念珠菌:820.7 μg/mL;热带草:809.9 μg/mL)。两种提取物均增强了氟康唑对白色念珠菌的抑制作用,但对热带念珠菌没有抑制作用。这些发现突出了这些提取物中次生代谢物的治疗潜力,加强了它们在开发新的抗菌和抗真菌策略中的重要性。
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来源期刊
Food and Chemical Toxicology
Food and Chemical Toxicology 工程技术-毒理学
CiteScore
10.90
自引率
4.70%
发文量
651
审稿时长
31 days
期刊介绍: Food and Chemical Toxicology (FCT), an internationally renowned journal, that publishes original research articles and reviews on toxic effects, in animals and humans, of natural or synthetic chemicals occurring in the human environment with particular emphasis on food, drugs, and chemicals, including agricultural and industrial safety, and consumer product safety. Areas such as safety evaluation of novel foods and ingredients, biotechnologically-derived products, and nanomaterials are included in the scope of the journal. FCT also encourages submission of papers on inter-relationships between nutrition and toxicology and on in vitro techniques, particularly those fostering the 3 Rs. The principal aim of the journal is to publish high impact, scholarly work and to serve as a multidisciplinary forum for research in toxicology. Papers submitted will be judged on the basis of scientific originality and contribution to the field, quality and subject matter. Studies should address at least one of the following: -Adverse physiological/biochemical, or pathological changes induced by specific defined substances -New techniques for assessing potential toxicity, including molecular biology -Mechanisms underlying toxic phenomena -Toxicological examinations of specific chemicals or consumer products, both those showing adverse effects and those demonstrating safety, that meet current standards of scientific acceptability. Authors must clearly and briefly identify what novel toxic effect (s) or toxic mechanism (s) of the chemical are being reported and what their significance is in the abstract. Furthermore, sufficient doses should be included in order to provide information on NOAEL/LOAEL values.
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