For many years, ergot alkaloids have been considered both a problem to be mitigated and a potential medical cure. These compounds have been primarily studied in the medical/pharmaceutical [1] and agricultural fields [2]. Depending on one’s perspective, the impact that ergot alkaloids have had on the progress of human medicine and livestock production can be either positive or negative. The dose or concentration of ergot alkaloid exposure is paramount. This can determine whether these compounds are implicated in the morbidity and mortality of individuals with St. Anthony’s Fire, or whether they can be used to treat migraines and post-partum bleeding; it can determine whether they are used to maximize plant resistance and persistence, or whether they constitute an animal welfare concern for grazing livestock [3,4]. The ethics of ergot alkaloid use is debated to this day, but there is no debating the impact of these compounds. Many of the positive and negative issues associated with ergot alkaloids have specific conditions with regional implications, but that does not diminish the magnitude of impact that these compounds have had on humans, livestock, and plants globally.
Research evaluating ergot alkaloids can be both basic and applied. Many types of research perspectives are necessary in understanding ergot alkaloids’ functions and how these findings might be applied. The focus of this Special Issue concerns original research and review articles that highlight benefits and detriments, and successes and failures involving ergot alkloids around the world with deference to regional distinctions. Research models range from fungus, to plant, to mammal; and the ergot alkaloids produced by both Claviceps and Epichloë spp. of fungi are included in this Special Issue. All submissions focus on ergot alkaloids’ effects (positive or negative) in different contexts. There is a benefit to this shared interest, even if the issues with ergot alkaloids do not directly overlap.
Significant advancements in the manipulation of plant–endophyte symbioses have been made in recent years to optimize the profile and concentration of the secondary compounds produced [5]. Eady [6] has reviewed the complexities plant breeders encounter when selecting a desired plant–endophyte symbiont, with New Zealand ryegrass as a model. This is a balance between selecting a source of ergot alkaloids that permit greater plant persistence, and inhibiting ergot alkaloid production that results in mycotoxicosis in grazing livestock in combination with desired plant traits. This makes the understanding of ergot alkaloid production paramount. The potential of using various-omics technologies to study ergot alkaloid production has been demonstrated in this Special Issue. In addition to traditional selection processes, Florea et al. [7] demonstrate the use of CRISPR technology to create a non-transgenic strain of Epichloë fungus without the genes necessary to produce ergot alkaloids. Fungi that produce ergot alkaloids can be endophytic and parasitic. Ergot contamination of cereal crops in Canadian provinces has become an issue of increasing concern. Hicks et al. [8] evaluate diversity in genes related to ergot alkaloid production in Canadian strains of the parasitic Claviceps purpurea to better characterize and understand the variation of ergot alkaloid content. Also looking at Canadian strains of C. purpurea, Liu et al. [9] evaluated the evolution patterns of gene clusters associated with different classes of ergot alkaloid production. Work of this caliber is critical to better understand this evolving issue.
Historically, human interactions with ergot alkaloids have been defined by large-scale poisonings through the consumption of contaminated grains [1]. Incidents of human ergot poisonings are increasingly rare due to improvements in crop management, grain screening and cleaning [10], and the regulation of safe quantities in food and feed [11]. However, there are still areas in the world where this can be an issue [12], and there is also still interest in the pharmaceutical potential of ergot alkaloids. Their most prominent use has been the treatment of migraines and controlling post-partum bleeding in the 18th and 19th centuries. In a current review of the past gynecological and obstetric uses of ergot alkaloids, Smakosz et al. [13] defined a potential role for the application of ergot alkaloids in modern obstetrics. In addition to clinical uses of ergot alkaloids, research assessing the sustainable production of ergot alkaloids in desirable formulations is needed. Shahid et al. [14] have developed a response surface methodology to select strains of Penicillium citrinum for their ability to produce ergot alkaloids in culture. Many researchers that study ergot alkaloids can relate to the challenges associated with obtaining purified forms of desired ergot alkaloids in any quantity.
Although medical applications focus on ergot alkaloids’ positive effects in humans, animal agriculture has historically and consistently viewed ergot alkaloids as a problem to be solved. Further, changing environmental conditions cause the ever-changing fungal production of ergot alkaloid profiles and concentrations. This necessitates routine surveys of grains and grasses. In this Special Issue, these are exemplified by the on-farm monitoring of ergot alkaloid levels in Kentucky horse pastures described by Lea and Smith [15], as well as the ergot alkaloids found in Slovenian feed grains, as described by Babic et al. [16]. Research of this nature is ongoing globally and contributes greatly to the mitigation of large-scale problems as well as the identification of future areas in need of research.
The variation of the content and concentration of ergot alkaloids is further complicated by livestock exposed to ergot alkaloids that demonstrate varied responses to the toxins. Poole et al. [17] and Wilbanks et al. [18] have studied various aspects, including genetics, that may make cattle more resistant to consumed ergot alkaloids. Ault-Seay et al. [19] used advanced-omics technologies to look at the rumen microbial and host metabolomes to provide a whole-animal characterization of impacts of ergot alkaloids. Mote and Filipov [20] reviewed the use of interactomics to provide a systemic understanding of the pathologies caused by ergot alkaloids that cause fescue toxicosis. A very specific pathology associated with ergot alkaloids and ergotism is a chronic vasoconstriction. Yonpaim et al. [21] looked at the acute exposure of ergot alkaloids on vasoactivity in ovine vasculature, and Valente et al. [22] evaluated prolonged ergot alkaloid exposure on the vasoactivity of bovine vasculature. Both studies [21,22] respectively evaluated aspects related to the ability of ergot alkaloids to interact with adrenergic and serotonergic receptors [23], and both papers concluded that receptor-mediated treatments for ergot alkaloid-induced vasoconstriction could be explored as potential therapies. From a systemic evaluation of ergot alkaloids’ impact on the whole animal or microbiome, to the study of a specific symptom, there is much yet to be learned about how ergot alkaloids disrupt mammalian physiology.
The collection of papers in the Global Impact of Ergot Alkaloids (https://www.mdpi.com/journal/toxins/special_issues/ergot_alkaloid) (accessed on 17 February 2022) Special Issue highlights the rich diversity of research and the complexity of the problems centered around ergot alkaloids. Although many specific issues related to accidental or intentional consumption of ergot alkaloids can be localized to a certain geographic region, the problems, challenges, and fascination with ergot alkaloids is global.
Acknowledgments
This editor is grateful to all the contributing authors. Their expertise and high-quality research made this special issue possible. Also, special thanks are extended to all the reviewers who provided rigorous reviews that have improved the content of this special issue. Lastly, I would like to thank the staff of MDPI Toxins journal for their patience and steadfast organization.
Funding
This research received no funding.
Conflicts of Interest
The author declares no conflict of interest.
Footnotes
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.
References
- 1.Schiff P.L. Ergot and its alkaloids. Am. J. Pharm. Educ. 2006;70:98. doi: 10.5688/aj700598. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Klotz J.L. Activities and Effects of Ergot Alkaloids on Livestock Physiology and Production. Toxins. 2015;7:2801–2821. doi: 10.3390/toxins7082801. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Strickland J.R., Looper M.L., Matthews J.C., Rosenkrans C.F., Jr., Flythe M.D., Brown K.R. Board-invited review: St. Anthony’s Fire in livestock: Causes, mechanisms, and potential solutions. J. Anim. Sci. 2011;89:1603–1626. doi: 10.2527/jas.2010-3478. [DOI] [PubMed] [Google Scholar]
- 4.Klotz J.L., Nicol A.M. Ergovaline, an endophytic alkaloid. 1. Animal physiology and metabolism. Anim. Prod. Sci. 2016;56:1761. doi: 10.1071/AN14962. [DOI] [Google Scholar]
- 5.Johnson L.J., de Bonth A.C.M., Briggs L.R., Caradus J.R., Finch S.C., Fleetwood D.J., Fletcher L.R., Hume D.E., Johnson R.D., Popay A.J., et al. The exploitation of epichloae endophytes for agricultural benefit. Fungal Divers. 2013;60:171–188. doi: 10.1007/s13225-013-0239-4. [DOI] [Google Scholar]
- 6.Eady C. The Impact of Alkaloid-Producing Epichloe Endophyte on Forage Ryegrass Breeding: A New Zealand Perspective. Toxins. 2021;13:158. doi: 10.3390/toxins13020158. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Florea S., Jaromczyk J., Schardl C.L. Non-Transgenic CRISPR-Mediated Knockout of Entire Ergot Alkaloid Gene Clusters in Slow-Growing Asexual Polyploid Fungi. Toxins. 2021;13:153. doi: 10.3390/toxins13020153. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Hicks C., Witte T.E., Sproule A., Lee T., Shoukouhi P., Popovic Z., Menzies J.G., Boddy C.N., Liu M., Overy D.P. Evolution of the Ergot Alkaloid Biosynthetic Gene Cluster Results in Divergent Mycotoxin Profiles in Claviceps purpurea Sclerotia. Toxins. 2021;13:861. doi: 10.3390/toxins13120861. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Liu M., Findlay W., Dettman J., Wyka S.A., Broders K., Shoukouhi P., Dadej K., Kolarik M., Basnyat A., Menzies J.G. Mining Indole Alkaloid Synthesis Gene Clusters from Genomes of 53 Claviceps Strains Revealed Redundant Gene Copies and an Approximate Evolutionary Hourglass Model. Toxins. 2021;13:799. doi: 10.3390/toxins13110799. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Flieger M., Wurst M., Shelby R. Ergot alkaloids—Sources, structures and analytical methods. Folia Microbiol. 1997;42:3–30. doi: 10.1007/BF02898641. [DOI] [PubMed] [Google Scholar]
- 11.EFSA Scientific Opinion on Ergot Alkaloids in Food and Feed. EFSA J. 2012;10:158. doi: 10.2903/j.efsa.2012.2798. [DOI] [Google Scholar]
- 12.Urga K., Debella A., W/Medihn Y., Agata N., Bayu A., Zewdie W. Laboratory studies on the outbreak of Gangrenous Ergotism associated with consumption of contaminated barley in Arsi, Ethiopia. Ethiop. J. Health Dev. 2002;16:317–323. doi: 10.4314/ejhd.v16i3.9800. [DOI] [Google Scholar]
- 13.Smakosz A., Kurzyna W., Rudko M., Dasal M. The Usage of Ergot (Claviceps purpurea (fr.) Tul.) in Obstetrics and Gynecology: A Historical Perspective. Toxins. 2021;13:492. doi: 10.3390/toxins13070492. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Shahid M.G., Nadeem M., Gulzar A., Saleem M., Rehman H.U., Ghafoor G.Z., Hayyat M.U., Shahzad L., Arif R., Nelofer R. Novel Ergot Alkaloids Production from Penicillium citrinum Employing Response Surface Methodology Technique. Toxins. 2020;12:427. doi: 10.3390/toxins12070427. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Lea K.M., Smith S.R. Using On-Farm Monitoring of Ergovaline and Tall Fescue Composition for Horse Pasture Management. Toxins. 2021;13:683. doi: 10.3390/toxins13100683. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Babic J., Tavcar-Kalcher G., Celar F.A., Kos K., Cervek M., Jakovac-Strajn B. Ergot and Ergot Alkaloids in Cereal Grains Intended for Animal Feeding Collected in Slovenia: Occurrence, Pattern and Correlations. Toxins. 2020;12:730. doi: 10.3390/toxins12110730. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.Poole D.H., Mayberry K.J., Newsome M., Poole R.K., Galliou J.M., Khanal P., Poore M.H., Serao N.V.L. Evaluation of Resistance to Fescue Toxicosis in Purebred Angus Cattle Utilizing Animal Performance and Cytokine Response. Toxins. 2020;12:796. doi: 10.3390/toxins12120796. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Wilbanks S.A., Justice S.M., West T., Klotz J.L., Andrae J.G., Duckett S.K. Effects of Tall Fescue Endophyte Type and Dopamine Receptor D2 Genotype on Cow-Calf Performance during Late Gestation and Early Lactation. Toxins. 2021;13:195. doi: 10.3390/toxins13030195. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Ault-Seay T.B., Melchior-Tiffany E.A., Clemmons B.A., Cordero J.F., Bates G.E., Flythe M.D., Klotz J.L., Ji H., Goodman J.P., McLean K.J., et al. Rumen and Serum Metabolomes in Response to Endophyte-Infected Tall Fescue Seed and Isoflavone Supplementation in Beef Steers. Toxins. 2020;12:744. doi: 10.3390/toxins12120744. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Mote R.S., Filipov N.M. Use of Integrative Interactomics for Improvement of Farm Animal Health and Welfare: An Example with Fescue Toxicosis. Toxins. 2020;12:633. doi: 10.3390/toxins12100633. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Yonpiam R., Gobbet J., Jadhav A., Desai K., Blakley B., Al-Dissi A. Vasoactive Effects of Acute Ergot Exposure in Sheep. Toxins. 2021;13:291. doi: 10.3390/toxins13040291. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Valente E.E.L., Harmon D.L., Klotz J.L. Influence of Prolonged Serotonin and Ergovaline Pre-Exposure on Vasoconstriction Ex Vivo. Toxins. 2021;14:9. doi: 10.3390/toxins14010009. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Berde B., Stürmer E. Introduction to the Pharmacology of Ergot Alkaloids and Related Compounds as a Basis of Their Therapeutic Action. Volume 49 Springer; Berlin/Heidelberg, Germany: 1978. [Google Scholar]