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Generic names in Magnaporthales

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Abstract

The order Magnaporthales comprises about 200 species and includes the economically and scientifically important rice blast fungus and the take-all pathogen of cereals, as well as saprotrophs and endophytes. Recent advances in phylogenetic analyses of these fungi resulted in taxonomic revisions. In this paper we list the 28 currently accepted genera in Magnaporthales with their type species and available gene and genome resources. The polyphyletic Magnaporthe 1972 is proposed for suppression, and Pyricularia 1880 and Nakataea 1939 are recommended for protection as the generic names for the rice blast fungus and the rice stem rot fungus, respectively. The rationale for the recommended names is also provided. These recommendations are made by the Pyricularia/Magnaporthe Working Group established under the auspices of the International Commission on the Taxonomy of Fungi (ICTF).
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volume 7 · no. 1
Generic names in Magnaporthales
Ning Zhang1, Jing Luo1, Amy Y. Rossman2, Takayuki Aoki3, Izumi Chuma4, Pedro W. Crous5, Ralph Dean6, Ronald P. de Vries5,7,
Nicole Donofrio8, Kevin D. Hyde9, Marc-Henri Lebrun10, Nicholas J. Talbot11, Didier Tharreau12, Yukio Tosa4, Barbara Valent13,
Zonghua Wang14, and Jin-Rong Xu15
1Department of Plant Biology and Pathology, Rutgers University, New Brunswick, NJ 08901, USA; corresponding author e-mail: zhang@aesop.
rutgers.edu
2Department of Botany and Plant Pathology, Oregon State University, Corvallis, Oregon 97331, USA
3Genetic Resources Center, National Agriculture and Food Research Organization, 2-1-2 Kannondai, Tsukuba, Ibaraki 305-8602, Japan
4Kobe University, 1-1 Rokkodai cho, Nada-ku, Kobe 657-8501, Japan
5CBS-KNAW Fungal Biodiversity Institute, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands
6Department of Plant Pathology, 2510 Thomas Hall, Raleigh, NC 27695, North Carolina State University, USA
7Fungal Molecular Physiology, Utrecht University, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands
8Department of Plant and Soil Sciences, University of Delaware, 531 S. College Ave, 152 Townsend Hall, Newark, DE 19711, USA
9Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai, Thailand
10UMR BIOGER, INRA, AgroParisTech, Université Paris-Saclay, 78850 Thiverval-Grignon, France
11University of Exeter, Northcote House, Exeter EX4 4QJ, UK
12UMR BGPI, CIRAD, TA A 54 K, 34398 Montpellier, France
13Department of Plant Pathology, Kansas State University, Manhattan, KS 66506-5502, USA
14Fujian Agriculture and Forestry University, Fuzhou 350002, Fujian, China
15Department of Botany and Plant Pathology, Purdue University, West Lafayette, IN 47907, USA
Abstract: The order Magnaporthales comprises about 200 species and includes the economically and
scientically important rice blast fungus and the take-all pathogen of cereals, as well as saprotrophs and
endophytes. Recent advances in phylogenetic analyses of these fungi resulted in taxonomic revisions. In this
paper we list the 28 currently accepted genera in Magnaporthales with their type species and available gene and
genome resources. The polyphyletic Magnaporthe 1972 is proposed for suppression, and Pyricularia 1880 and
Nakataea 1939 are recommended for protection as the generic names for the rice blast fungus and the rice stem
rot fungus, respectively. The rationale for the recommended names is also provided. These recommendations
are made by the Pyricularia/Magnaporthe Working Group established under the auspices of the International
Commission on the Taxonomy of Fungi (ICTF).
Article info: Submitted: 2 March 2016; Accepted: 15 May 2016; Published: 8 June 2016.
INTRODUCTION
Magnaporthales (Sordariomycetes, Ascomycota) contains
important pathogens of cereals and grasses, including the
rice blast fungus Pyricularia oryzae (Magnaporthe oryzae),
the take-all pathogen of cereals Gaeumannomyces graminis,
the rice stem rot pathogen Nakataea oryzae (Magnaporthe
salvinii) and the summer patch pathogen of turf grass
Magnaporthiopsis poae (Cannon 1994, Thongkantha et al.
2009). To date, about 200 species have been described in
Magnaporthales, of which approximately 50 % are pathogens
of domesticated and wild monocotyledons.
The rice blast fungus has conidial (asexual) and ascosporic
(sexual) morphs and the rice stem rot fungus produces
sclerotial (asexual), conidial (asexual) and ascosporic
(sexual) morphs. Historically, such pleomorphy added to the
difculty in resolving taxonomic and nomenclatural problems
associated with these species.
Recent advancement in gene, transcriptome and genome
sequencing of Magnaporthales fungi resulted in robust
phylogenies, which correspond well with the pathogenicity,
ecology and biology of these species. However, the
phylogenies conict with certain traditional generic concepts
based on morphology. Magnaporthe and Gaeumannomyces,
for example, were shown to be polyphyletic. Taxonomic
revisions have been carried out for some of these taxa in
recent publications (Luo & Zhang 2013, Klaubauf et al.
2014, Luo et al. 2015a). In this paper, we list 28 accepted
genera in Magnaporthales and provide the rationale for the
recommended genera if there is competition.
Key words:
Ascomycota
Magnaporthe
Nakataea
one fungus-one name
pleomorphic fungi
Pyricularia
rice blast
take-all
doi:10.5598/imafungus.2016.07.01.09 IMA FUNGUS · 7(1): 155–159 (2016)
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A list of accepted generic names in Magnaporthales, with
the type species, is compiled in Table 1 including references
that serve as the basis for recognizing these genera. This
follows approval of their usage by the Pyricularia/Magnaporthe
Working Group, without prejudice. Cases that require action
to be approved by the Nomenclature Committee for Fungi
(NCF) are indicated by an asterisk in that Table.
RECOMMENDATIONS
(A) = a name typied by an asexual morph, (S) = a name
typied by a sexual morph.
Use Nakataea Hara 1939 (A) rather than
Magnaporthe R.A. Krause & R.K. Webster 1972
(S)
Cattaneo (1876) rst named the rice stem rot pathogen as
Sclerotium oryzae based on the sclerotial morph. In the same
paper he also described Leptosphaeria salvinii, which was
later recognized as the sexual morph of the same fungus
(Tullis 1933). Hara (1939) named the conidial morph of the
species Nakataea sigmoidea. Krause & Webster (1972) then
established the new generic name Magnaporthe, typied by the
ascosporic morph, to accommodate the rice stem rot pathogen
as Magnaporthe salvinii, as necessitated by the nomenclatural
rules then in force. Sclerotium and Leptosphaeria currently
belong in Basidiomycota and Dothideomycetes respectively
(Xu et al. 2010), and are therefore not applicable to this
sordariomycetous species. Nakataea and Magnaporthe are
congeneric and their type species, Nakataea sigmoidea and
Magnaporthe salvinii, refer to the same species (Krause &
Webster 1972). Subsequent to the ending of the separate
naming of morphs of the same fungus species in 2011, under
Art. 59.1 of the International Code of Nomenclature for algae,
fungi, and plants (ICN; McNeill et al. 2012), Luo et al. (2013)
made a new combination for the rice stem rot fungus as
Nakataea oryzae, using the oldest legitimate generic name
and species epithet. Those authors did not, however, formally
propose the rejection or suppression of the later sexually
typied names as currently required by Art. 57.2. We note that
it is proposed that this requirement be eliminated from the ICN
in 2017 (Hawksworth 2015), but it is currently in force.
Use Pyricularia oryzae Cavara 1892 (A) rather
than Magnaporthe oryzae (Catt.) B.C. Couch
2002 (S)
In 1880, Saccardo established the generic name Pyricularia
based on the asexually typied P. grisea on crabgrass. The
rice isolates were designated as P. oryzae in 1892 by Cavara,
which now is known as the rice blast fungus. Since then, over
50 species have been listed as Pyricularia that cause blast
diseases of monocotyledonous plants.
The sexual morph of Pyricularia was rst observed in
1970 from laboratory crossing experiments and believed to
belong to Magnaporthe because of the similarity in ascospore
morphology (Hebert 1970, Barr 1977, Couch & Kohn 2002).
However, recent phylogenetic and phylogenomic analyses
demonstrated that the sexually typied genus Magnaporthe
was polyphyletic. The rice blast fungus is not congeneric
with the type species of Magnaporthe, M. salvinii, and the
placement of the rice blast fungus in Magnaporthe was
based on an incorrect morphological identication (Zhang et
al. 2011, Luo & Zhang 2013, Luo et al. 2014, Murata et al.
2014, Luo et al. 2015a). This is not a nomenclatural issue
because the generic names Magnaporthe and Pyricularia are
not congeneric and so do not compete for priority.
Pyricularia and Magnaporthe are currently both widely used
generic names, and the rice blast fungus is an economically
and scientically important species that deserves much
caution. The Pyricularia/Magnaporthe Working Group has
considered the possibility of conserving the name Magnaporthe
over Pyricularia. However, such conservation would require a
change in the type species of the genus Magnaporthe, and
would cause numerous name changes for those species
currently placed in Pyricularia.
The asexually typied generic name Pyricularia is the
correct name for the rice blast fungus, which corresponds well
with pathogenicity and ecological and evolutionary features.
The name Pyricularia oryzae should therefore be used for
the rice blast fungus. The synonym Magnaporthe oryzae,
can nevertheless continue to be mentioned in publications
as “Pyricularia oryzae (syn. Magnaporthe oryzae)”. This
practice will help to bridge a potential gap in the literature and
knowledge for this important species.
Use Clasterosporium Schwein. 1832 (A) rather
than Clasterosphaeria Sivan. 1984 (S)
The generic name Clasterosphaeria, typied by C. cyperi,
was established for the sexual morph of Clasterosporium
cyperi and includes only two names. The generic name
Clasterosporium based on C. caricinum includes 158
names, many of which have been placed in other genera.
Whether or not Clasterosphaeria cyperi is congeneric with
Clasterosporium caricinum is not known, although this seems
likely given that both occur on Cyperaceae. If this is the
case, use of the older, more commonly used generic name
Clasterosporium is recommended.
Use Gaeumannomyces Arx & D.L. Olivier 1952
(S) rather than Harpophora Gams 2000 (A)
The generic name Gaeumannomyces, typied by G.
graminis, has long been used for the cause of take-all of
wheat disease (Walker 1972, 1980). Harpophora was
established for phialophora-like species that were known
to be asexual morphs related to Gaeumannomyces
and Magnaporthe but did not produce a sexual morph
(Gams 2000). With the change to one name, Harpophora
based on H. radicicola is to be considered a synonym of
Gaeumannomyces, based on phylogeny (Luo et al. 2015b).
Given the greater number of species, priority, and numerous
reports, we see no reason not to use the rst published
name, Gaeumannomyces.
ACKNOWLEDGMENTS
This work was partially supported by the National Science Foundation
of the United States (grant number DEB 1145174 and DEB 1452971)
to Ning Zhang.
Generic names in Magnaporthales
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Table 1. Accepted generic names in Magnaporthales with type species, number of species in each genus, and gene or genomic resources.
Names needing approval are indicated by an asterisk (*).
Taxa Type species Number of
species
GenBank accession numbers for gene and
genome sequence data**
MAGNAPORTHACEAE
Buergenerula Syd. in Annls
mycol. 34: 392. 1936.
Buergenerula biseptata
(Rostr.) Syd. 1936.
(Metasphaeria biseptata
Rostr. 1904).
4Buergenerula spartinae: transcriptome (SRX798618)
(Luo et al. 2015a).
Bussabanomyces Klaubauf et
al. in Stud. Mycol. 79: 100. 2014.
Bussabanomyces
longisporus (Bussaban)
Klaubauf et al. 2014.
(Pyricularia longispora
Bussaban 2003).
1Bussabanomyces longisporus: transcriptome
(SRX798619) (Luo et al. 2015a).
Ceratosphaerella Huhndorf et al.
in Mycologia 100: 941. 2008.
Ceratosphaerella
castillensis (C.L. Sm.)
Huhndorf et al. 2008.
2Ceratosphaerella castillensis: ITS (EU527997), LSU
(EU528003) (Huhndorf et al. 2008).
Ceratosphaeria Niessl in Verh.
nat. Ver. Brünn 14: 203. 1876.
Ceratosphaeria
lampadophora (Berk. &
Broome) Niessl 1876.
34 Ceratosphaeria lampadophora: ITS (AY761088),
LSU (AY346270) (Huhndorf et al. 2008).
* Clasterosporium Schwein. in
Trans. Am. phil. Soc., New Series
4: 300. 1832.
Clasterosporium caricinum
Schwein. 1832.
158
= Clasterosphaeria Sivan. in
Trans. Brit. mycol. Soc. 83: 710.
1984.
Clavatisporella K.D. Hyde in
Mycotaxon 55: 276. 1995.
Clavatisporella musicola
K.D. Hyde 1995.
1
Falciphora J. Luo & N. Zhang in
Mycologia 107: 643. 2015.
Falciphora oryzae (Z.L.
Yuan et al.) J. Luo & N.
Zhang 2015.
1Falciphora oryzae genome (JNVV01000000) (Xu et
al. 2014).
Gaeumannomyces Arx & D.L.
Olivier in Trans. Brit. mycol. Soc.
35: 32. 1952.
Gaeumannomyces
graminis var. graminis
(Sacc.) Arx & D.L. Olivier
1952.
7Gaeumannomyces graminis var. avenae:
transcriptome (SRX798620) (Luo et al. 2015a);
Gaeumannomyces graminis var. graminis:
transcriptome (SRX798621) (Luo et al. 2015a);
Gaeumannomyces graminis var. tritici: genome
(ADBI00000000) (Okagaki et al. 2015).
= Harpophora W. Gams in Stud.
Mycol. 45: 192. 2000.
Herbampulla Scheuer &
Nograsek in Mycotaxon 47: 419.
1993.
Herbampulla crassirostris
Scheuer & Nograsek 1993
1
Kohlmeyeriopsis Klaubauf et al.
in Stud. Mycol. 79: 101. 2014.
Kohlmeyeriopsis
medullaris (Kohlm., Volkm.-
Kohlm. & O.E. Erikss.)
Klaubauf et al. 2014.
1Kohlmeyeriopsis medullaris: SSU(FJ176801),
ITS(KM484852), LSU(FJ176801), RPB1(KM485069)
(Klaubauf et al. 2014).
Magnaporthiopsis J. Luo & N.
Zhang in Mycologia 105: 1021.
2013.
Magnaporthiopsis poae
(Landsch. & N. Jacks.) J.
Luo & N. Zhang 2013.
5Magnaporthiopsis incrustans: genome (SRX795321),
transcriptome (SRX798625) (Luo et al. 2015a);
Magnaporthiopsis panicorum: transcriptome
(SRX798626) (Luo et al. 2015a);
Magnaporthiopsis poae: genome (ADBL01000000)
(Okagaki et al. 2015);
Magnaporthiopsis rhizophila: genome (SRX798599),
transcriptome (SRX798627) (Luo et al. 2015a).
Muraeriata Huhndorf et al. in
Mycologia 100: 948. 2008.
Muraeriata collapsa
Huhndorf, Greif, Mugambi &
A.N. Mill. 2008.
2Muraeriata collapsa: LSU (EU527996) (Huhndorf et
al. 2008).
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Table 1. (Continued).
Taxa Type species Number of
species
GenBank accession numbers for gene and
genome sequence data**
* Nakataea Hara, Diseases Rice
Plant, 2nd : 185. 1939.
Nakataea oryzae (Catt.) J.
Luo & N. Zhang 2013.
7Nakataea oryzae: genome (SRX798605),
transcriptome (SRX798628) (Luo et al. 2015a).
= Magnaporthe R.A. Krause &
R.K. Webster in Mycologia 64:
110. 1972.
Omnidemptus P.F. Cannon &
Alcorn in Mycotaxon 51: 483.
1994.
Omnidemptus afnis P.F.
Cannon & Alcorn 1994.
1Omnidemptus afnis: transcriptome (SRX798629)
(Luo et al. 2015a).
Pseudophialophora J. Luo &
N. Zhang in Mycologia 106: 581.
2014.
Pseudophialophora
eragrostis J. Luo & N.
Zhang 2014.
8Pseudophialophora eragrostis: transcriptome
(SRX798634) (Luo et al. 2015a);
Pseudophialophora panicorum: transcriptome
(SRX798635) (Luo et al. 2015a);
Pseudophialophora schizachyrii: transcriptome
(SRX798637) (Luo et al. 2015a).
Pyriculariopsis M.B. Ellis,
Demat. Hyphom.: 206. 1971.
Pyriculariopsis parasitica
(Sacc. & Berl.) M.B. Ellis
1971.
1Pyriculariopsis parasitica: LSU(DQ341514) (Klaubauf
et al. 2014).
Slopeiomyces Klaubauf et al. in
Stud. Mycol. 79: 102. 2014.
Slopeiomyces
cylindrosporus (D. Hornby
et al.) Klaubauf et al. 2014.
1Slopeiomyces cylindrosporus: transcriptome
(SRX798639) (Luo et al. 2015a).
OPHIOCERACEAE
Ophioceras Sacc., Syll. Fung. 2:
358. 1883.
Ophioceras
dolichostomum (Berk. &
M.A. Curtis) Sacc. 1883.
33 Ophioceras dolichostomum: genome (SRX798611)
(Luo et al. 2015a);
Ophioceras commune: transcriptome (SRX798630)
(Luo et al. 2015a);
Ophioceras leptosporum: transcriptome
(SRX798632) (Luo et al. 2015a).
Pseudohalonectria Minoura &
T. Muroi in Trans. Mycol. Soc.
Japan 19: 132. 1978.
Pseudohalonectria
lignicola Minoura & T. Muroi
1978.
13 Pseudohalonectria lignicola: genome (SRX798616),
transcriptome (SRX798633) (Luo et al. 2015a).
PYRICULARIACEAE
Bambusicularia Klaubauf et al.
in Stud. Mycol. 79: 104. 2014.
Bambusicularia brunnea
Klaubauf et al. 2014.
1Bambusicularia brunnea: ITS(KM484830),
LSU(KM484948), ACT(AB274449), CAL(AB274482),
RPB1(KM485043) (Klaubauf et al. 2014).
Barretomyces Klaubauf et al. in
Stud. Mycol. 79: 104. 2014.
Barretomyces calatheae
(D.J. Soares et al.) Klaubauf
et al. 2014.
1Barretomyces calatheae: ITS(KM484831),
LSU(KM484950), ACT(KM485162),
CAL(KM485231), RPB1(KM485045) (Klaubauf et al.
2014).
Deightoniella S. Hughes in
Mycol. Pap. 48: 27. 1952.
Deightoniella africana S.
Hughes 1952.
20
Macgarvieomyces Klaubauf et
al. in Stud. Mycol. 79: 106. 2014.
Macgarvieomyces borealis
(de Hoog & Oorschot)
Klaubauf et al. 2014.
2Macgarvieomyces borealis: SSU(DQ341511),
ITS(KM484854), LSU(DQ341511), ACT(KM485170),
CAL(KM485239), MCM7(KM009174),
RPB1(KM485070), TEF1(KM009198) (Klaubauf et
al. 2014, Luo et al. 2015a);
Macgarvieomyces juncicola: transcriptome
sequenced (SRX798624) (Luo et al. 2015a).
Neopyricularia Klaubauf et al. in
Stud. Mycol. 79: 108. 2014.
Neopyricularia
commelinicola (M.J. Park
& H.D. Shin) Klaubauf et al.
2014.
1Neopyricularia commelinicola: SSU(KM009211),
ITS(FJ850122), LSU(KM484985), ACT(KM485175),
CAL(KM485243), MCM7(KM009175),
RPB1(KM485087), TEF1(KM009199) (Klaubauf et
al. 2014, Luo et al. 2015a).
Proxipyricularia Klaubauf et al.
in Stud. Mycol. 79: 109. 2014.
Proxipyricularia zingiberis
(Y. Nisik.) Klaubauf et al.
2014.
1Proxipyricularia zingiberis: ITS(KM484869),
LSU(KM484986), ACT(AB274448), CAL(KM485244),
RPB1(KM485088) (Klaubauf et al. 2014).
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Table 1. (Continued).
Taxa Type species Number of
species
GenBank accession numbers for gene and
genome sequence data**
Pseudopyricularia Klaubauf et
al. in Stud. Mycol. 79: 109. 2014.
Pseudopyricularia
kyllingae Klaubauf et al.
2014.
3Pseudopyricularia kyllingae: ITS(KM484876),
LSU(KM484992), ACT(AB274451), CAL(AB274484),
RPB1(KM485096) (Klaubauf et al. 2014).
Pyricularia Sacc. in Michelia 2:
20. 1880.
Pyricularia grisea Sacc.
1880.
55 Pyricularia grisea: transcriptome (SRX798638) (Luo
et al. 2015a); genome (PRJEB7653 at http://genome.
jouy.inra.fr/gemo/)
Pyricularia oryzae:
Genome (Dean et al. 2005).
Xenopyricularia Klaubauf et al.
in Stud. Mycol. 79: 116. 2014.
Xenopyricularia zizaniicola
(Hashioka) Klaubauf et al.
2014.
1Xenopyricularia zizaniicola: transcriptome
(SRX798640) (Luo et al. 2015a).
** Unpublished genome data are not listed.
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... Finally, another mycovirus infectious transcript allowed the dissection of the very interesting virus symbiotic lifestyle discussed later (see Rosellinia viruses, below). An infectious clone of the Yado-kari positivestrand virus was verified to be dependent on Yado-nushi co-infection to complete its life cycle (Zhang et al. 2016b). ...
... The virus mentioned above (Transfection with nucleic acid) characterized by a novel mutualistic lifestyle between two unrelated viruses, was first described in R. necatrix by Suzuki and colleagues. In this instance, one virus yado-kari virus 1 (YkV1; yado-kari meaning "borrowing a room"), an ssRNA virus, was hypothesized to use the capsid of an unrelated dsRNA virus, yadonushi virus 1 (YnV1; yado-nushi meaning "room owner"), and use it as a base for replication and genome encapsidation (Zhang et al. 2016b) (reviewed in Hisano et al. 2018). The yado-kari/ yado-nushi hypothesis was supported by later experiments showing that, indeed, YkV1 used its own encoded RdRp enzyme to replicate its RNA, but in YnV1-encoded capsids (Das et al. 2021). ...
... In another study, upregulation of ochratoxin production by A. ochraceus was also linked to the presence of a specific partitivirus (Nerva et al. 2018). Recently tenuazonic acid production was also shown to be induced by a totivirus infection in Pyricularia oryzae (Magnaporthales; previous name is Magnaporthe oryzae) (Zhang et al. 2016b). The upregulation of a specific transcription factor involved in the teA synthetase gene upregulation is the proposed molecular mechanism behind the upregulation (Ninomiya et al. 2020). ...
Chapter
Mycoviruses are the viruses that infect fungi and the unrelated stramenopiles such as oomycetes that have morphologies and lifestyles similar to fungi. Our knowledge of mycoviruses and their effects on the biology of their hosts has exploded in recent years. Although the field only started to mature in the 1980s and 1990s, advances in technology coupled with the promise of mycoviruses for biological control of fungi pathogenic to plants, animals, and humans led to increased attention and dedicated research. Mycoviruses are now classified within at least 16 virus families, and that number grows continually as new viruses that do not fit within the current taxonomy are described. This chapter highlights some of the most important fungal virus systems, and some of the advances in our understanding of mycoviruses, especially in the context of their effects on host biology and fitness.
... Our aim was to work with varieties that shared similar growing cycle length but exhibited a diversity of morphological traits and resistance to Pyricularia oryzea (Zhang et al., 2016;Qi et al., 2019) in order to evaluate the effects of their mixtures under contrasting field conditions. Four upland rice varieties were selected for the experiment: EARLY MUTANT IAC 165 (A), FOFIFA 152 (B), FOFIFA 154 (C), and DOURADO PRECOCE (D). ...
... Specifically, EARLY MUTANT IAC 165 and DOURADO PRECOCE are taller than FOFIFA 152 and FOFIFA 154. Additionally, according to the previous study, variety A proved to be the most productive, while D exhibited the highest sensitivity to Pyricularia oryzea (Zhang et al., 2016;Qi et al., 2019). ...
... Throughout the experiment, striga infestation, Pyricularia oryzea (Zhang et al., 2016;Qi et al., 2019) and Bacterial leaf Blight (BLB) caused by Xanthomonas oryzae pv. oryzae (Xoo) incidence (Tall et al., 2022) were recorded. ...
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Introduction Rice plays a critical role in human livelihoods and food security. However, its cultivation requires inputs that are not accessible to all farming communities and can have negative effects on ecosystems. simultaneously, ecological research demonstrates that biodiversity management within fields contributes to ecosystem functioning. Methods This study aims to evaluate the mixture effect of four functionally distinct rice varieties in terms of characteristics and agronomic performance and their spatial arrangement on the upland rice performance in the highlands of Madagascar. The study was conducted during the 2021-2022 rainfall season at two close sites in Madagascar. Both site differ from each other’s in soil properties and soil fertility management. The experimental design at each site included three modalities: i) plot composition, i.e., pure stand or binary mixture; ii) the balance between the varieties within a mixture; iii) and for the balanced mixture (50% of each variety), the spatial arrangement, i.e., row or checkerboard patterns. Data were collected on yields (grain and biomass), and resistance to Striga asiatica infestation, Pyricularia oryzea and bacterial leaf blight (BLB) caused by Xanthomonas oryzae-pv from each plot. Results and discussion Varietal mixtures produced significantly higher grain and biomass yields, and significantly lower incidence of Pyricularia oryzea compared to pure stands. No significant differences were observed for BLB and striga infestation. These effects were influenced by site fertility, the less fertilized site showed stronger mixture effects with greater gains in grain yield (60%) and biomass yield (42%). The most unbalanced repartition (75% and 25% of each variety) showed the greatest mixture effect for grain yield at both sites, with a strong impact of the varietal identity within the plot. The mixture was most effective when EARLY_MUTANT_IAC_165 constituted 75% of the density associated with other varieties at 25% density. The assessment of the net effect ratio of disease, an index evaluating the mixture effect in disease reduction, indicated improved disease resistance in mixtures, regardless of site conditions. Our study in limited environments suggests that varietal mixtures can enhance rice productivity, especially in low-input situations. Further research is needed to understand the ecological mechanisms behind the positive mixture effect.
... Rice (Oryza sativa L.) is one of the important cereals contributing signifi cantly to the world's food suffi ciency, this is true because more than half the world's population consumes rice as the main staple [1]. Its productivity is usually affected by many major and minor diseases [2], Among them, the blast caused by Magnaporthe oryzae (synonym-Pyricularia oryzae) [3] is the most severe resulting into great losses globally. ...
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Blast resistance tends to often break down, these necessitate search-resistant genes. The screen house experiment was conducted in 2019 and 2020. A total of 56 rice genotypes, (Elite lines, monogenic lines, and local), were screened against ten Kenya isolates of Mangnaporthe oryzae. The establishment was by direct seeding of previously sprouted seeds. A completely Randomized Design (CRD) with two replicates was adopted. Inoculation was done 21 days after planting. Plants were maintained in the moist chamber (26–28 0C) for 48 hrs, then moved into an incubation chamber (25 ◦C ± 2). Disease assessment commenced 48 hours after inoculation until 21 days to full infection. Disease evaluations were performed according to the Standard Evaluation System of IRRI. Polymerase Chain Reactions (PCR) were carried out, blast resistant loci were identified using varied genetic markers that co-segregate with specific resistant loci Analysis was implemented in R version 3.3.2 (R Core Team, 2016). BLUPs were computed, in a mixed model to estimate the random effect of the genotypes. The data was subjected to analysis of variance and means separated by Tukey’s test at P < 0.05. Cluster analyses were performed in JMP software version 11.2 for Windows. Seven genotypes (IR12A311, IR10M210, IR74, 1R02A127, IR09A130, R66 and IR10N230) were more susceptible, IR13N152 and IR14F711 were more resistant to all Isolates. The monogenic lines IRBLsh-B and IRBLkh-K3 which carry blast-resistant genes, were susceptible to at least seven Kenya isolates. The local checks (Basmati 370, BAS 270 (pi9), BW196, and BAS370 (pi9) were highly susceptible. The genotype IR12F711 was consistently resistant to all Kenya Isolates.
... The rice blast fungus Magnaporthe oryzae (synonym of Pyricularia oryzae) causes the most devastating disease of rice worldwide (Zhang et al. 2016;Wang et al. 2009), with losses estimated at $66 billion (Pennisi 2010). In the USA alone-a country responsible for only 1-2% of global rice production-fungicides worth $70 million are needed each year to control rice blast disease (Nalley et al. 2016;Cruz and Valent 2017). ...
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Septin GTPases are morphogenetic proteins that are widely conserved in eukaryotic organisms fulfilling diverse roles in cell division, differentiation and development. In the filamentous fungal pathogen Magnaporthe oryzae , the causal agent of the devastating blast diseases of rice and wheat, septins have been shown to be essential for plant infection. The blast fungus elaborates a specialised infection structure called an appressorium with which it mechanically ruptures the plant cuticle. Septin aggregation and generation of a hetero-oligomeric ring structure at the base of the infection cell is indispensable for plant infection. Furthermore, once the fungus enters host tissue it develops another infection structure, the transpressorium, enabling it to move between living host plant cells, which also requires septins for its function. Specific inhibition of septin aggregation—either genetically or with chemical inhibitors—prevents plant infection. Significantly, by screening for inhibitors of septin aggregation, broad spectrum anti-fungal compounds have been identified that prevent rice blast and a number of other cereal diseases in field trials. We review the recent advances in our understanding of septin biology and their potential as targets for crop disease control.
... Penggunaan agen hayati sebagai agen biopriming juga dapat menekan pertumbuhan jamur patogen penyebab penyakit pada tanaman padi. Salah satu penyakit yang menyerang tanaman padi yaitu penyakit blas daun yang disebabkan oleh Magnaporthe oryzae yang mampu menembus kutikula luar daun padi dan menyerang jaringan tanaman hidup (Zhang et al., 2016). Blas daun dapat berkembang dengan cepat sehingga mengganggu penyerapan unsur hara dan pertumbuhan tanaman padi dan berpotensi menyebabkan kematian tanaman padi apabila kondisi lingkungan mendukung pertumbuhan patogen (Dewi et al., 2013). ...
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Priming is a seed-soaking technique to increase seed viability and also suppress pathogens' growth. Magnaporthe oryzae is one of the pathogens in rice plants that causes leaf blast disease. The high rice consumption each year in Indonesia is not proportional to the amount of rice plant production, which is affected by the growth of pathogenic fungi. This study aims to determine the viability and percentage inhibition of Bacillus subtilis and Trichoderma harzianum against the growth of the pathogenic fungus Magnaporthe oryzae on local West Sumatra rice varieties Ceredek, Pandan Pulau, and Batang Sungkai. The research was conducted by testing the viability of microbes by counting the number of colonies and testing microbial antagonists with the Dual Culture method on seven days of observation. The results showed that Bacillus subtilis and Trichoderma harzianum could inhibit the growth of the pathogen M. oryzae, which causes leaf blast disease. The viability of Bacillus subtilis after biopriming for 48 hours was most significant on Ceredek variety, which was 15.9x106 cfu/g, and for Trichoderma harzianum on Pandan Pulau variety, which was 0.4x106 cfu/g. The most significant inhibition percentage of Bacillus subtilis and Trichoderma harzianum was obtained in Ceredek rice with a value of 30.13% (medium category) and 63.04% (high category).
... Rice blast is the major rice disease [81] caused by fungi of the genus Pyricularia (Sordariomycetes, Magnaporthales) belonging to the Pyricularia grisea complex [82,83]. This species complex provisionally accommodates the problematic status of P. grisea sensu stricto and Pyricularia oryzae. ...
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The concept of fastidious microorganisms currently found in scientific literature is mainly related to the difficulty of isolating/culturing/preserving bacteria. Eukaryotes are investigated much less in this respect, although they represent a fundamental part of the microbial world. Furthermore, not only isolation, but also identification and culturing (in the perspective of long-term preservation) should be considered key aspects often impacting on the study of fastidious microorganisms, especially in terms of preservation in culture collections and biotechnological exploitation. The present review aimed to investigate the current state of the art on fastidious eukaryotes, with special emphasis on the efforts to improve their isolation, identification, culturing and long-term preservation in culture collections practices. A few case studies focused on some fastidious eukaryotic microorganisms (including possible customized solutions to overcome specific issues) are also presented: isolation and preservation of slow-growing fungi, culturing of Haematococcus lacustris, isolation of unialgal strains of Cyanidiophytina (Rhodophyta), identification of Metschnikowia pulcherrima clade yeasts, isolation and preservation of Pyricularia species, preservation of Halophytophtora spp.
... Appressoria facilitate pathogen entry into host tissue to cause disease, and the famous 'gold leaf' experiment demonstrated the capacity of some fungal appressoria to puncture the leaf surface using force generation rather than enzymatic activity 2,4 . Appressoria of the rice blast fungus Magnaporthe oryzae (synonym of Pyricularia oryzae) 5 -a major threat to global food security 6-8 -breach the tough surface of rice leaves and, remarkably, other hard synthetic surfaces by generating turgor of up to 8.0 MPa (~40 times the pressure of a car tyre 9 ). This generates force at the base of the appressorium, measured in a related pathogen Colletotrichum graminicola using an optical waveguide, of 17 µN (ref. ...
Article
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The rice blast fungus Magnaporthe oryzae uses a pressurized infection cell called an appressorium to drive a rigid penetration peg through the leaf cuticle. The vast internal pressure of an appressorium is very challenging to investigate, leaving our understanding of the cellular mechanics of plant infection incomplete. Here, using fluorescence lifetime imaging of a membrane-targeting molecular mechanoprobe, we quantify changes in membrane tension in M. oryzae. We show that extreme pressure in the appressorium leads to large-scale spatial heterogeneities in membrane mechanics, much greater than those observed in any cell type previously. By contrast, non-pathogenic melanin-deficient mutants, exhibit low spatially homogeneous membrane tension. The sensor kinase ∆sln1 mutant displays significantly higher membrane tension during inflation of the appressorium, providing evidence that Sln1 controls turgor throughout plant infection. This non-invasive, live cell imaging technique therefore provides new insight into the enormous invasive forces deployed by pathogenic fungi to invade their hosts, offering the potential for new disease intervention strategies.
... Given that rice provides 23% of the calories to humankind and is a staple food for half of the world's population, controlling rice blast in a sustainable manner would constitute a major contribution to global food security. Rice blast is caused by the filamentous fungus Magnaporthe oryzae (synonym of Pyricularia oryzae) (Zhang et al., 2016) which has evolved the ability to breach the tough outer cuticle of rice leaves and invade living plant tissue. M. oryzae can also infect a wide range of grass hosts and cause diseases, such as A C C E P T E D M A N U S C R I P T 3 wheat blast, an emerging threat to wheat (Triticum aestivum) production (Urashima. ...
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The rice blast fungus Magnaporthe oryzae causes a devastating disease that threatens global rice (Oryza sativa) production. Despite intense study, the biology of plant tissue invasion during blast disease remains poorly understood. Here we report a high resolution, transcriptional profiling study of the entire plant-associated development of the blast fungus. Our analysis revealed major temporal changes in fungal gene expression during plant infection. Pathogen gene expression could be classified into 10 modules of temporally co-expressed genes, providing evidence for the induction of pronounced shifts in primary and secondary metabolism, cell signalling and transcriptional regulation. A set of 863 genes encoding secreted proteins are differentially expressed at specific stages of infection, and 546 genes named MEP (Magnaporthe effector protein) genes were predicted to encode effectors. Computational prediction of structurally-related MEPs, including the MAX effector family, revealed their temporal co-regulation in the same co-expression modules. We characterised 32 MEP genes and demonstrate that Mep effectors are predominantly targeted to the cytoplasm of rice cells via the biotrophic interfacial complex (BIC) and use a common unconventional secretory pathway. Taken together, our study reveals major changes in gene expression associated with blast disease and identifies a diverse repertoire of effectors critical for successful infection.
... Rice blast, caused by the ascomycete Pyricularia oryzae (synonym Magnaporthe oryzae, [1,2]), is one of the most damaging fungal diseases of rice at the World scale [3]. It causes lesions to all aerial parts of the plant, mainly leaves and panicles, resulting in yield losses, sometimes up to 100% under favorable environmental conditions [4] and equivalent to the food of 60 million people annually [5]. ...
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Citation: Zampieri, E.; Volante, A.; Marè, C.; Orasen, G.; Desiderio, F.; Biselli, C.; Canella, M.; Carmagnola, L.; Milazzo, J.; Adreit, H.; et al. Marker-Assisted Pyramiding of Blast-Resistance Genes in a japonica Elite Rice Cultivar through Forward and Background Selection. Plants 2023, 12, 757. https://doi. Abstract: Rice blast, caused by Pyricularia oryzae, is one of the main rice diseases worldwide. The pyramiding of blast-resistance (Pi) genes, coupled to Marker-Assisted BackCrossing (MABC), provides broad-spectrum and potentially durable resistance while limiting the donor genome in the background of an elite cultivar. In this work, MABC coupled to foreground and background selections based on KASP marker assays has been applied to introgress four Pi genes (Piz, Pib, Pita, and Pik) in a renowned japonica Italian rice variety, highly susceptible to blast. Molecular analyses on the backcross (BC) lines highlighted the presence of an additional blast-resistance gene, the Pita-linked Pita2/Ptr gene, therefore increasing the number of blast-resistance introgressed genes to five. The recurrent genome was recovered up to 95.65%. Several lines carrying four (including Pita2) Pi genes with high recovery percentage levels were also obtained. Phenotypic evaluations confirmed the effectiveness of the pyramided lines against multivirulent strains, which also had broad patterns of resistance in comparison to those expected based on the pyramided Pi genes. The developed blast-resistant japonica lines represent useful donors of multiple blast-resistance genes for future rice-breeding programs related to the japonica group.
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There is a recent unparalleled increase in demand for rice in sub-Saharan Africa, yet its production is affected by blast disease. Characterization of blast resistance in adapted African rice cultivars can provide important information to guide growers and rice breeders. We used molecular markers for known blast resistance genes ( Pi genes; n = 21) to group African rice genotypes ( n = 240) into similarity clusters. We then used greenhouse-based assays to challenge representative rice genotypes ( n = 56) with African isolates ( n = 8) of Magnaporthe oryzae which varied in virulence and genetic lineage. The markers grouped rice cultivars into five blast resistance clusters (BRC) which differed in foliar disease severity. Using stepwise regression, we found that the Pi genes associated with reduced blast severity were Pi50 and Pi65, whereas Pik-p, Piz-t, and Pik were associated with increased susceptibility. All rice genotypes in the most resistant cluster, BRC 4, possessed Pi50 and Pi65, the only genes that were significantly associated with reduced foliar blast severity. Cultivar IRAT109, which contains Piz-t, was resistant against seven African M. oryzae isolates, whereas ARICA 17 was susceptible to eight isolates. The popular Basmati 217 and Basmati 370 were among the most susceptible genotypes. These findings indicate that most tested genes were not effective against African blast pathogen collections. Pyramiding genes in the Pi2/9 multifamily blast resistance cluster on chromosome 6 and Pi65 on chromosome 11 could confer broad-spectrum resistance capabilities. To gain further insights into genomic regions associated with blast resistance, gene mapping could be conducted with resident blast pathogen collections. [Formula: see text] Copyright © 2023 The Author(s). This is an open access article distributed under the CC BY-NC-ND 4.0 International license .
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Magnaporthaceae is a family of ascomycetes that includes three fungi of great economic importance: Magnaporthe oryzae, Gaeumannomyces graminis var. tritici, and Magnaporthe poae. These three fungi cause widespread disease and loss in cereal and grass crops including rice blast disease (M. oryzae), take-all disease in wheat and other grasses (G. graminis), and summer patch disease in turf grasses (M. poae). Here, we present the finished genome sequence for M. oryzae and draft sequences for M. poae and G. graminis var. tritici. We used multiple technologies to sequence and annotate the genomes of M. oryzae, M. poae, and G. graminis var. tritici. The M. oryzae genome is now finished to 7 chromosomes while M. poae and G. graminis var. tritici are sequenced to 40.0X and 25.0X coverage respectively. Gene models were developed using multiple computational techniques and further supported by RNAseq data. In addition, we performed preliminary analysis of genome architecture and repetitive element DNA.
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The order Magnaporthales (Ascomycota, Fungi) includes devastating pathogens of cereals, such as the rice blast fungus Pyricularia (Magnaporthe) oryzae, which is a model in host-pathogen interaction studies. Magnaporthales also includes saprotrophic species associated with grass roots and submerged wood. Despite its scientific and economic importance, the phylogenetic position of Magnaporthales within Sordariomycetes and the interrelationships of its constituent taxa, remain controversial. In this study, we generated novel transcriptome data from 21 taxa that represent key Magnaporthales lineages of different infection and nutrition modes and phenotypes. Phylogenomic analysis of >200 conserved genes allowed the reconstruction of a robust Sordariomycetes tree of life that placed the monophyletic group of Magnaporthales sister to Ophiostomatales. Among Magnaporthales, three major clades were recognized: 1) an early diverging clade A comprised of saprotrophs associated with submerged woods; 2) clade B that includes the rice blast fungus and other pathogens that cause blast diseases of monocot plants. These species infect the above-ground tissues of host plants using the penetration structure, appressorium; and 3) clade C comprised primarily of root-associated species that penetrate the root tissue with hyphopodia. The well-supported phylogenies provide a robust framework for elucidating evolution of pathogenesis, nutrition modes, and phenotypic characters in Magnaporthales.
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We investigated the phylogenetic relationships among Magnaporthales fungi with harpophora-like asexual states based on DNA sequences of ITS, MCM7, RPB1 and TEF1 genes. The results indicated that these species are polyphyletic. Based on the four-gene phylogeny, the type species of Harpophora, H. radicicola, belongs to Gaeumannomyces and thus Harpophora is treated as a synonym of Gaeumannomyces. In addition a monotypic new genus, Falciphora, is established based on F. oryzae, previous referred as Harpophora oryzae. Copyright © 2015, Mycologia.
Article
Magnaporthe oryzae is described as a new species distinct from M. grisea. Gene trees were inferred for Magnaporthe species using portions of three genes: actin, beta-tubulin, and calmodulin. These gene trees were found to be concordant and distinguished two distinct clades within M. grisea. One clade is associated with the grass genus Digitaria and is therefore nomenclaturally tied to M. grisea. The other clade is associated with Oryza sativa and other cultivated grasses and is described as a new species, M. oryzae. While no morphological characters as yet distinguish them, M. oryzae is distinguished from M. grisea by several base substitutions in each of three loci as well as results from laboratory matings; M.oryzae and M. grisea are not interfertile. Given that M. oryzae is the scientifically correct name for isolates associated with rice blast and grey leaf spot, continued use of M. grisea for such isolates would require formal nomenclatural conservation.
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A morphological study of Magnaporthe salvinii gen. nov., comb, nov., the cause of stem rot of rice, disclosed that it had unitunicate, shortstalked, thin-walled, deliquescent asci with a light-refractive ring surrounding the pore. The ontogeny of the paraphyses-like bands found in the centrum was studied and the term reliquiae proposed for this tissue. The genus Magnaporthe was established in the Diaporthales to accommodate this fungus. Magnaporthe salvinii was found heterothallic.
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The phragmosporous genera Magnaporthe and Telimenella are placed in the Physosporellaceae. Ceratosphaeria grisea is transferred to Magnaporthe and Telimenella phacidioidea is newly described. The differences between Hyponectria and Physalospora, both amerosporous genera of the family, are clarified. The species assigned to Hyponectria are separated in a key and are briefly described. The new species H. betulina and H. gregaria are introduced; Laestadia auripunctum, Sphaeria cooptera, Sphaerella depressa, Guignardia lonicerae, Sphaeria magnoliae, Guignardia populi, and Laestadia rubescens are transferred to Hyponectria.
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Phialophora is a little-differentiated genus of more or less pigmented, phialidic hyphomycetes. With the addition of numerous species, it has become highly polyphyletic, comprising anamorphs of discomycetes, pyrenomycetes and loculoascomycetes. The core of the genus consists of anamorphs of Capronia in the Herpotrichiellaceae, Chaetothyriales. Some taxa have already been segregated from Phialophora into genera such as Lecythophora (Coniochaetaceae) and Phaeoacremonium (Magnaporthaceae?). Ascomycete orders in which phialophora-like fungi have been placed are reviewed, and some further segregation is proposed. For the common anamorphs of the discomycete family Dermateaceae, the old generic name Cadophora is available and should be used for Ph. fastigiata and related taxa (one new combination). For anamorphs of Gaeumannomyces and Magnaporthe (Magnaporthaceae), a new genus, Harpophora, is proposed with four new combinations. Criteria that allow a correlation with the suggested broad-scale subdivision are outlined.