Abstract

The order Magnaporthales belongs to Sordariomycetes, Ascomycota. Magnaporthales includes five families, namely Ceratosphaeriaceae, Pseudohalonectriaceae, Ophioceraceae, Pyriculariaceae, and Magnaporthaceae. Most Magnaporthales members are found in Poaceae plants and other monocotyledonous herbaceous plants ubiquitously as plant pathogens or endophytic fungi, and some members are found in decaying wood or dead grass as saprophytic fungi. Therefore, studying the biogeography and ecology of Magnaporthales is of great significance. Here, we described the biodiversity of endophytic Magnaporthales fungi from Poaceae at three latitudes in China and conducted a meta-analysis of the geography and ecology of Magnaporthales worldwide. We found that Magnaporthales is a dominant order in the endophytic fungi of Poaceae. More than half of the endophytic Magnaporthales fungi have a taxonomically uncertain placement. Notably, few endophytic fungi are grouped in the clusters with known saprophytic or pathogenic Magnaporthales fungi, indicating that they may have saprophytic and parasitic differentiation in nutritional modes and lifestyles. The meta-analysis revealed that most species of Magnaporthales have characteristic geographical, host, and tissue specificity. The geographical distribution of the three most studied genera, namely Gaeumannomyces, Magnaporthiopsis, and Pyricularia, in Magnaporthales may depend on the distribution of their hosts. Therefore, studies on the endophytic fungal Magnaporthales from monocotyledonous plants, including Poaceae, in middle and low latitudes will deepen our understanding of the biogeography and ecology of Magnaporthales.

Highlights

  • The aims of the present study were: (1) to determine the phylogenetic relationships of endophytic Magnaporthales fungi from Poaceae in three geographic origins using a five-loci sequence, including the internal transcribed spacer of ribosomal DNA (ITS), large subunit of ribosomal DNA (LSU), DNA replication licensing factor (MCM7), RPB1, and translation elongation factor 1 (TEF1) as well as to analyze the relationship between endophytic Magnaporthales fungi and their host tissues and sites; and (2) to conduct a meta-analysis of the global geographic distribution of the genera of Magnaporthales and the species of Gaeumanomyces, Magnaporthiopsis, and Pyricularia, as well as to analyze the relationships between various species of Magnaporthales and their hosts and tissues

  • The multi-loci phylogenetic tree (Figure 1) showed five main clusters corresponding to Pseudohalonectriaceae, Ceratosphaeriaceae, Ophioceraceae, Pyriculariaceae, and Magnaporthaceae

  • We found that most species, except unidentified Pseudophialophora clade 1 and Ophioceras leptosporum, had host specificity

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Summary

Introduction

Thongkantha et al (2009) first introduced the new order Magnaporthales to accommodate Magnaporthaceae, based on the results of morphology and phylogenetic analysis of the large subunit of ribosomal DNA (LSU) and the small subunit of ribosomal DNA (SSU). Klaubauf et al (2014) separated Pyricularia and its related genera and Ophioceras and its related genera from Magnaporthaceae and introduced two separate families, Pyriculariaceae and Ophioceraceae, respectively, to accommodate them, according to morphological observation and two-loci phylogenetic analysis of LSU and the large subunit of RNA polymerase II (RPB1). Based on four-loci phylogenetic analysis of LSU, SSU, translation elongation factor 1 (TEF1), and the second largest subunit of RNA polymerase (RPB2), Maharachchikumbura et al (2016) accepted three families in Magnaporthales, Magnaporthaceae, Ophioceraceae, and Pyriculariaceae, and placed Pseudohalonectria in the genera incertae sedis of Magnaporthale. According to a multi-loci phylogenetic analysis of LSU, RPB2, and TEF1, Luo et al (2019) introduced a new family Ceratosphaeriaceae in Magnaporthales to accommodate Ceratosphaeria, and raised Distoseptisporaceae to a new order Distoseptisporales

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