Harnessing functions of the microbiota to combat fungal pathogens
Yun Chen1, Sunde Xu1, Tomislav Cernava2, Yang Bai3 1State Key Laboratory of Rice Biology, Key Laboratory of Molecular Biology of Crop Pathogens and Insects, Department of Plant Protection, Zhejiang University, Hangzhou, China. 2Institute of Environmental Biotechnology, Graz University of Technology, Graz, Austria. 3State Key Laboratory of Plant Genomics, CAS-JIC Centre of Excellence for Plant and Microbial Science, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, China.
Fusarium graminearum is a widespread pathogenic fungus that causes Fusarium head blight (FHB) in cereal crops worldwide, especially in wheat1. Between 2000 and 2018, an annual average of more than 4.5 million hectares were affected by FHB in China, or around 20% of the total planted area of wheat. This has resulted in annual production losses of more than 3.41 million tons2.
Wheat heads with Fusarium head blight symptoms on a few spikelets (left-hand panel), and the fungal fruiting body on a stubble (right-hand panel).
Fusarium head blight epidemics not only reduce global wheat production, but also contaminate grains with mycotoxins that threaten human and livestock health 2. To infect new hosts, F. graminearum must often endure a period of dormancy (winter) and produce spores at the right time to ensure the survival of the next pathogen generation. The main propagation strategy of this monocyclic pathogen is formation of ascospores in perithecia (fungal fruiting bodies), which are then ejected and spread via wind, insect, and rain dissemination3. Therefore, interfering with perithecium formation to decrease the initial inoculum seemed to be a promising strategy for FHB management. The screening for biological control agents (BCAs) and their application was evaluated in the frame of this study as a viable alternative and ecologically friendly method for perithecium suppression. Fungal structures are known to provide microhabitats for adapted bacterial populations, just like soil, plants, and animals. Members of bacterial communities that are intrinsically associated with plant-pathogenic fungi were therefore hypothesized to be a promising source of BCAs against highly destructive pathogens. We assumed that these bacteria likely possess advantages in terms of their adaptability to survive and proliferate on fungal structures.
Schematic visualization of bacterial communities on the fungal perithecia
In our study, we found that F. graminearum perithecia provided a specific ecological niche for bacteria that could play an important role in disease establishment. Over 2000 bacterial strains were isolated from the native microbiota of F. graminearum, and subsequently identified and screened for antagonistic activity. We were successful in this approach and recovered 113 isolates that showed antagonistic activity against the pathogen. One specific bacterial isolate, termed as ZJU23, was identified as Pantoea agglomerans, and had the strongest inhibitory ability against F. graminearum among all isolates. Subsequently, we showed that herbicolin A secreted by ZJU23 is responsible for the observed suppression of F. graminearum.
Although herbicolin A was identified about four decades ago4,5, its biosynthetic gene cluster and mode of action against fungi were not known. In our study, we set out to investigate the biosynthetic gene cluster and mode of action against various fungi by combining various approaches, including transposon mutagenesis, liquid chromatography-mass spectrometry, atomic force microscopy and confocal microscopy. By comparing the metabolic profiles of ZJU23 and four deletion mutants of a potential biosynthesis gene cluster, we found that herbicolin A was synthesized by the AcbA-AcbJ cluster. We then proceeded to uncover the mode of action of herbicolin A against various fungi. It is important to note that the modes of action of cyclic lipopeptides against fungi are mostly unknown. What surprised us is that herbicolin A was shown to disrupt lipid rafts by interacting with ergosterol, which resulted in the formation of abnormal cell membranes, and, ultimately, caused cell death. Herbicolin A also was also found to inhibit the growth of Candida albicans and Aspergillus fumigatus, and was more effective than the clinical fungicides Amphotericin B and fluconazole. This provided important evidence for potential applications of herbicolin A beyond agriculture, for example in medicine.
Overall, we have deciphered the mechanism of the inhibitory effect of herbicolin A on fungi and identified its biosynthetic gene cluster. This could support future developments for sustainable management of Fusarium head blight worldwide.
Proposed model for the mode of action of herbicolin A secreted by ZJU23 in the fungal perithecium microbiome.
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