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| LETTER TO EDITOR |
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| Year : 2020 | Volume
: 9
| Issue : 2 | Page : 109-110 |
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Bitter taste receptor agonists to abate the bitterness of genital infections: A hype or hope?
Menizibeya O Welcome
Department of Physiology, Faculty of Basic Medical Sciences, Nile University of Nigeria, Abuja, Nigeria
| Date of Submission | 26-Oct-2019 |
| Date of Decision | 18-Dec-2019 |
| Date of Acceptance | 29-Dec-2019 |
| Date of Web Publication | 30-Mar-2020 |
Correspondence Address:
Menizibeya O Welcome
Department of Physiology, Faculty of Basic Medical Sciences, Nile University of Nigeria, Abuja
Nigeria
 Source of Support: None, Conflict of Interest: None
DOI: 10.4103/2305-0500.281081
How to cite this article:
Welcome MO. Bitter taste receptor agonists to abate the bitterness of genital infections: A hype or hope?. Asian Pac J Reprod 2020;9:109-10 |
How to cite this URL:
Welcome MO. Bitter taste receptor agonists to abate the bitterness of genital infections: A hype or hope?. Asian Pac J Reprod [serial online] 2020 [cited 2023 Feb 4];9:109-10. Available from: https://www.apjr.net/text.asp?2020/9/2/109/281081 |
Dear Editor,
Genital infections are associated with high level of morbidity, economic and psychosocial burden. Several millions of new cases are reported annually among people aged 15–49 years. The complications of genital infections include chronic neurological diseases, end stage renal disease in adults, ectopic pregnancy, premature delivery and stillbirth [1]. Indeed, genital infections account for about 15%–35% and 50%–75% of infertility cases in males and females respectively [2]. Despite the awareness campaign and substantial improvement in medical treatment, the incidence of genital infections has continued to increase over the past years. Without doubt, this negative trend corroborates the necessity to search for alternative areas that may lead to discovery of novel therapy for genital infections.
Bitter taste receptors (T2Rs), first discovered in the gastrointestinal tract, are now believed to be widely expressed in several cells and tissues of the body where they play diverse roles in sensing toxins and also serve as immune sentinels. Recently, T2R expression was reported in cells, tissues and organs of the genital system: cervix, vagina, endometrium, myometrium, placenta, ovary, prostate, testis, and spermatozoa [3],[4]. T2Rs are transmembrane G protein-coupled receptors that sense bitter compounds by activating a-gustducin, which signals downstream cell, mediating responses that subsequently lead to the activation of defense mechanisms, which are aimed at abating the pathogenic aggression. This is why T2Rs are now referred to as critical components of the sensory and immune system. To date, twenty five subtypes of human T2Rs have been discovered. T2Rs are activated by bitter molecules including caffeine, amarogentin, and denatonium. There are currently more than 1 000 known bitter compounds [5] and numerous naturally occurring ones mainly derived from plant sources [6]. These T2R agonists present potential application in drug discovery and therapeutics of genital infections.
In the genital tract, T2Rs are readily activated by the microbial compounds – quorum sensing signal molecules, produced by bacteria (Gram-positive and Gram-negative), parasites, and virus to regulate biofilm formation, motility and virulence [7],[8]. Interestingly, about 50% of the microbial genome and 80% of microbial motility are regulated by quorum sensing signal molecules. Examples of quorum sensing signal molecules include a- hydroxyketones, acyl homoserine lactones, alkylquinolones, autoinducers, autoinducing peptides, and diffusible signal factors, among others [8]. The SigMol database contains all currently known quorum sensing signal molecules [8].
The T2Rs regulate microbial aggression in the genital tract by actively interacting with bitter molecules and products of microbial pathogens, and perhaps with the genital microflora. Consequently, the genital T2Rs act as immune sentinels by mediating cellular responses and activating protective mechanisms against pathogenic aggression in the genital system [3],[4].
The expressions of T2Rs in genital epithelial cells and spermatozoa suggest a role of these receptors in sensing the genital fluidic milieu for harmful and pathogenic components to mobilize responses against genital infections [3]. Importantly, T2R signaling disorders in spermatozoa were reportedly associated with multiple damages caused by Pseudomonas aeruginosa [7]. Truly, data demonstrate that genital T2Rs detect not only bitter compounds but also the uropathogenic Escherichia coli to initiate cellular and tissue responses that prevent the colonization of the genital tract by pathogens [9]. The presence of T2Rs in the endometrium and myometrium suggests their possible roles in the pathogenesis of endometritis and myometritis respectively. For example, Zheng et al reported that the T2R agonist, chloroquine, prevented bacterial lipopolysaccharide-induced endometritis, myometritis, chorioamnionitis and villitis in pregnant experimental animals [10]. These findings indicate a critical role of T2Rs in the pathophysiology of preterm labor and stillbirth induced by uterine infections. Thus, the placental T2Rs not only prevent harmful substances from getting to the conceptus, but also play a critical role in inflammatory processes occurring in the placenta. A schematic representation of bitter taste receptor responses to agonist stimulation in the genital tract is depicted in [Figure 1]. | Figure 1: Schematic representation of bitter taste receptor signaling in the genital tract. T2Rs: bitter taste receptors; IP3: inositol triphosphate; PKC: protein kinase C; PKA: protein kinase A; NO: nitric oxide; NOS: nitric oxide synthase; L-Arg: L-arginine; NF-kB: nuclear factor kappa B.
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From the emerging evidence presented above, it can be summarized that effective detection of bitter compounds or pathogenic products by T2Rs constitutes a critical mechanism in the prevention of genital tract infections. Since the mechanisms of quorum sensing are actively been researched for novel antimicrobial therapy to the control resistant microbial species [7],[8], research crusade aimed at investigating the signaling pathways of genital T2Rs can lead to identification of key molecular targets for novel therapeutics of genital infections. Thus, there is a need to step up investigations on the molecular mechanisms of T2R sensing of the “quorum” and “suppression of pathogenic aggression” in the genital tract for novel medical application.
Conflict of interest statement
There is no conflict of interest regarding the publication of this paper.
Author’s contributions
Menizibeya O. Welcome wrote the paper.
| References | |  |
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| 2. | Solomon M, Henkel R. Semen culture and the assessment of genitourinary tract infections. Indian J Urol 2017; 33: 188-193. |
| 3. | Xu J, Cao J, Iguchi N, Riethmacher D, Huang L. Functional characterization of bitter-taste receptors expressed in mammalian testis. Mol Hum Reprod 2013; 19 (1): 17-28. |
| 4. | Wölfle U, Elsholz FA, Kersten A, Haarhaus B, Schumacher U, Schempp CM. Expression and functional activity of the human bitter taste receptor TAS2R38 in human placental tissues and JEG-3 cells. Molecules 2016; 21: 306. |
| 5. | Wiener A, Shudler M, Levit A, Niv MY. Bitter DB: A database of bitter compounds. Nucleic Acids Res 2012; 40: D413-D419. |
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| 7. | Rennemeier C, Frambach T, Hennicke F, Dietl J, Staib P. Microbial quorum-sensing molecules induce acrosome loss and cell death in human spermatozoa. Infect Immun 2009; 77 (11): 4990-4997. |
| 8. | Rajput A, Kaur K, Kumar M. SigMol: Repertoire of quorum sensing signaling molecules in prokaryotes. Nucleic Acids Res 2016; 44 (D1): D634-D639. |
| 9. | Deckmann K, Filipski K, Krasteva-Christ G, Fronius M, Althaus M, Rafiq A, et al. Bitter triggers acetylcholine release from polymodal urethral chemosensory cells and bladder reflexes. PNAS 2014; 111 (22): 8287-8292. |
| 10. | Zheng K, Lu P, Delpapa E, Bellve K, Deng R, Condon JC, et al. Bitter taste receptors as targets for tocolytics in preterm labor therapy. FASEB J 2017; 31 (9): 4037-4052. |
[Figure 1]
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