Study on the Inhibitory Effect and Mechanism of Trans-2-Decenal on Helicobacter pylori in vitro
Abstract
Objective
To investigate the in vitro inhibitory and bactericidal activities of the trans-2-decenal compound against Helicobacter pylori (H. pylori) and explore its potential mechanism.
Methods
The minimal inhibitory concentration (MIC) and minimal bactericidal concentration (MBC) of trans-2-decenal against H. pylori clinical isolates and the standard strain ATCC43504 were determined using the broth microdilution method. Changes in MIC values were monitored to assess drug resistance in H. pylori induced by continuous treatment with trans-2-decenal. The synergistic antibacterial effect of combining trans-2-decenal with antibiotics such as metronidazole (MTZ), clarithromycin (CLA), amoxicillin (AMX), and levofloxacin (LEV) was evaluated using the fractional inhibitory concentration index (FICI). After treating standard H. pylori strains with trans-2-decenal, scanning electron microscopy, transmission electron microscopy, crystal violet staining, the semi-solid puncture method, and the Berthelot method were used to assess the effects of trans-2-decenal on the morphology, cell structure, migration, and urease activity of H. pylori.
Results
The MIC range for clinically resistant H. pylori strains C907, C101, R1, R2, R4, R10, R16, R24, R36, and R40 was 8-16 μg/mL, with an MBC range of 16-32 μg/mL. The MIC for the H. pylori standard strain ATCC43504 was 16 μg/mL, with an MBC of 16 μg/mL.Trans-2-decenal inhibits H. pylori at low concentrations for short durations and does not easily induce H. pylori resistance. Trans-2-decenal reduces the required dosage of antibiotics (metronidazole and levofloxacin), showing an additive effect. Trans-2-decenal alters the shape of H. pylori and promotes bacterial rupture. Furthermore, Trans-2-decenal exerts its effects by altering H. pylori morphology, inducing bacterial rupture, inhibiting biofilm formation, reducing the number of mature biofilms, and decreasing urease activity and H. pylori migration ability.
Conclusion
Trans-2-decenal may inhibit H. pylori in vitro through multiple mechanisms and is unlikely to promote the development of H. pylori resistance.
Keywords: Helicobacter pylori, Trans-2-decenal, Antibacterial activity, In vitro
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LI Y, CHOI H, LEUNG K, et al. Global prevalence of Helicobacter pylori infection between 1980 and 2022: a systematic review and meta-analysis. Lancet Gastroenterol Hepatol, 2023, 8(6): 553-564. doi: 10.1016/S2468-1253(23)00070-5.
TSHIBANGU-KABAMBA E, YAMAOKA Y. Helicobacter pylori infection and antibiotic resistance - from biology to clinical implications. Nat Rev Gastroenterol Hepatol, 2021, 18(9): 613-629. doi: 10.1038/s41575-021-00449-x.
SUN Q, YUAN C, ZHOU S, et al. Helicobacter pylori infection: a dynamic process from diagnosis to treatment. Front Cell Infect Microbiol, 2023, 13: 1257817. doi: 10.3389/fcimb.2023.1257817.
TANG Q, MA Z, TANG X, et al. Coptisine inhibits Helicobacter pylori and reduces the expression of CagA to alleviate host inflammation in vitro and in vivo. J Ethnopharmacol, 2023, 314: 116618. doi: 10.1016/j.jep.2023. 116618.
ARSLAN N, YILMAZ O, DEMIRAY-GURBUZ E. Importance of antimicrobial susceptibility testing for the management of eradication in Helicobacter pylori infection. World J Gastroenterol, 2017, 23(16): 2854-2869. doi: 10.3748/wjg.v23.i16.2854.
BANG C S, BAIK G H. Attempts to enhance the eradication rate of Helicobacter pylori infection. World J Gastroenterol, 2014, 20(18): 5252-5262. doi: 10.3748/wjg.v20.i18.5252.
NG H Y, LEUNG W K, CHEUNG K S. Antibiotic Resistance, Susceptibility Testing and Stewardship in Helicobacter pylori Infection. Int J Mol Sci, 2023, 24(14): 11702. doi: 10.3390/ijms241411708.
LI Z J, NJATENG G S, HE W J, et al. Chemical composition and antimicrobial activity of the essential oil from the edible aromatic plant Aristolochia delavayi. Chem Biodivers, 2013, 10(11): 2032-2041. doi: 10. 1002/cbdv.201300066.
KUMAR S, AHMAD R, SAEED S, et al. Chemical Composition of Fresh Leaves Headspace Aroma and Essential Oils of Four Coriander Cultivars. Front Plant Sci, 2022, 13: 820644. doi: 10.3389/fpls.2022.820644.
WU X, WEI F, DING F, et al. Phytochemical analysis, antioxidant, antimicrobial, and anti-enzymatic properties of Alpinia coriandriodora (sweet ginger) rhizome. Front Plant Sci, 2023, 14: 1284931. doi: 10.3389/fpls.2023.1284931.
HE Q Y N, PAN M L, TIAN H Y, et al. Study on drug resistance and virulence genes of Helicobacter pylori in patients with failed eradication therapy. Modern Preventive Medicine, 2024, 51(7): 1331-1337. doi: 10. 20043/j.cnki.MPM.202401036.
ZULLO A, IERARDI E, HASSAN C, et al. Furazolidone-based therapies for Helicobacter pylori infection: a pooled-data analysis. Saudi J Gastroenterol, 2012, 18(1): 11-17. doi: 10.4103/1319-3767.91729.
GODERSKA K, AGUDO PENA S, ALARCON T. Helicobacter pylori treatment: antibiotics or probiotics. Appl Microbiol Biotechnol, 2018, 102(1): 1-7. doi: 10.1007/s00253-017-8535-7.
TRAN TRUNG H, TRUONG THI HUYNH H, NGUYEN THI THUY L, et al. Growth-Inhibiting, Bactericidal, Antibiofilm, and Urease Inhibitory Activities of Hibiscus rosa sinensis L. Flower Constituents toward Antibiotic Sensitive- and Resistant-Strains of Helicobacter pylori. ACS Omega, 2020, 5(32): 20080-20089. doi: 10.1021/acsomega.0c01640.
DEMIRTAS A, OZTURK H, SUDAGIDAN M, et al. Effects of commercial aldehydes from green leaf volatiles (green odour) on rumen microbial population and fermentation profile in an artificial rumen (Rusitec). Anaerobe, 2019, 55: 83-92. doi: 10.1016/j.anaerobe.2018.11.001.
WANG Y C. Medicinal plant activity on Helicobacter pylori related diseases. World J Gastroenterol, 2014, 20(30): 10368-10382. doi: 10.3748/wjg.v20.i30.10368.
SALINAS IBANEZ A G, ORIGONE A L, LIGGIERI C S, et al. Asclepain cI, a proteolytic enzyme from Asclepias curassavica L. , a south American plant, against Helicobacter pylori. Front Microbiol, 2022, 13: 961958. doi: 10.3389/fmicb.2022.961958.
YAN J, PENG C, CHEN P, et al. In-vitro anti-Helicobacter pylori activity and preliminary mechanism of action of Canarium album Raeusch. fruit extracts. J Ethnopharmacol, 2022, 283: 114578. doi: 10.1016/j.jep.2021. 114578.
IERARDI E, LOSURDO G, MILETI A, et al. The puzzle of coccoid forms of helicobacter pylori: Beyond basic science. Antibiotics (Basel), 2020, 9(6): 293. doi: 10.3390/antibiotics9060293.
LIAN D W, XU Y F, DENG Q H, et al. Effect of patchouli alcohol on macrophage mediated Helicobacter pylori digestion based on intracellular urease inhibition. Phytomedicine, 2019, 65: 153097. doi: 10.1016/j. phymed.2019.153097.
XU Y F, LIAN D W, CHEN Y Q, et al. In vitro and in vivo antibacterial activities of patchouli alcohol, a naturally occurring tricyclic sesquiterpene, against Helicobacter pylori infection. Antimicrob Agents Chemother, 2017, 61(6): e00122-00117. doi: 10.1128/AAC.00122-17.
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