Species Discrimination within the Metarhizium PARB Clade: Ribosomal Intergenic Spacer (rIGS)-Based Diagnostic PCR and Single Marker Taxonomy

Author:

Schuster Christina1,Baró Robaina Yamilé12ORCID,Ben Gharsa Haifa1,Bobushova Saikal3,Manfrino Romina Guadalupe14ORCID,Gutierrez Alejandra C.4ORCID,Lopez Lastra Claudia C.4,Doolotkeldieva Tinatin3,Leclerque Andreas1ORCID

Affiliation:

1. Department of Biology, Technische Universität Darmstadt (TUDa), Schnittspahnstraße 10, 64287 Darmstadt, Germany

2. Plant Health Research Institute (INISAV), 110 Str. 514, Havana 11600, Cuba

3. Faculty of Agriculture, Kyrgyz-Turkish Manas University, 56 Chyngyz Aitmatov Avenue, Bishkek 720038, Kyrgyzstan

4. Centro de Estudios Parasitólogicos y de Vectores (CEPAVE), CONICET-Consejo Nacional de Investigaciones Científicas y Técnicas, UNLP-Universidad Nacional de La Plata, La Plata 1900, Argentina

Abstract

(1) Background: The entomopathogenic fungus Metarhizium anisopliae sensu lato forms a species complex, comprising a tight cluster made up of four species, namely M. anisopliae sensu stricto, M. pinghaense, M. robertsii and M. brunneum. Unambiguous species delineation within this “PARB clade” that enables both the taxonomic assignment of new isolates and the identification of potentially new species is highly solicited. (2) Methods: Species-discriminating primer pairs targeting the ribosomal intergenic spacer (rIGS) sequence were designed and a diagnostic PCR protocol established. A partial rIGS sequence, referred to as rIGS-ID800, was introduced as a molecular taxonomic marker for PARB species delineation. (3) Results: PARB species from a validation strain set not implied in primer design were clearly discriminated using the diagnostic PCR protocol developed. Using rIGS-ID800 as a single sequence taxonomic marker gave rise to a higher resolution and statistically better supported delineation of PARB clade species. (4) Conclusions: Reliable species discrimination within the Metarhizium PARB clade is possible through both sequencing-independent diagnostic PCR and sequencing-dependent single marker comparison, both based on the rIGS marker.

Funder

German Ministry of Education and Research

Ministerio de Ciencia Tecnología y Medio Ambiente

Ministerio de Agricultura

German Academic Exchange Service

Publisher

MDPI AG

Subject

Plant Science,Ecology, Evolution, Behavior and Systematics,Microbiology (medical)

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