New Fungus-Insect Symbiosis: Culturing, Molecular, and Histological Methods Determine Saprophytic Polyporales Mutualists of Ambrosiodmus Ambrosia Beetles.
Ambrosia symbiosis is an obligate, farming-like mutualism between wood-boring beetles and fungi. It evolved at least 11 times and includes many notorious invasive pests. All ambrosia beetles studied to date cultivate ascomycotan fungi: early colonizers of recently killed trees with poor wood digesti...
Main Authors: | , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2015-01-01
|
Series: | PLoS ONE |
Online Access: | http://europepmc.org/articles/PMC4569427?pdf=render |
id |
doaj-c34709402ae74ec09438f1725e16481c |
---|---|
record_format |
Article |
spelling |
doaj-c34709402ae74ec09438f1725e16481c2020-11-25T01:25:09ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01109e013768910.1371/journal.pone.0137689New Fungus-Insect Symbiosis: Culturing, Molecular, and Histological Methods Determine Saprophytic Polyporales Mutualists of Ambrosiodmus Ambrosia Beetles.You LiDavid Rabern SimmonsCraig C BatemanDylan P G ShortMatthew T KassonRobert J RabagliaJiri HulcrAmbrosia symbiosis is an obligate, farming-like mutualism between wood-boring beetles and fungi. It evolved at least 11 times and includes many notorious invasive pests. All ambrosia beetles studied to date cultivate ascomycotan fungi: early colonizers of recently killed trees with poor wood digestion. Beetles in the widespread genus Ambrosiodmus, however, colonize decayed wood. We characterized the mycosymbionts of three Ambrosiodmus species using quantitative culturing, high-throughput metabarcoding, and histology. We determined the fungi to be within the Polyporales, closely related to Flavodon flavus. Culture-independent sequencing of Ambrosiodmus minor mycangia revealed a single operational taxonomic unit identical to the sequences from the cultured Flavodon. Histological sectioning confirmed that Ambrosiodmus possessed preoral mycangia containing dimitic hyphae similar to cultured F. cf. flavus. The Ambrosiodmus-Flavodon symbiosis is unique in several aspects: it is the first reported association between an ambrosia beetle and a basidiomycotan fungus; the mycosymbiont grows as hyphae in the mycangia, not as budding pseudo-mycelium; and the mycosymbiont is a white-rot saprophyte rather than an early colonizer: a previously undocumented wood borer niche. Few fungi are capable of turning rotten wood into complete animal nutrition. Several thousand beetle-fungus symbioses remain unstudied and promise unknown and unexpected mycological diversity and enzymatic innovations.http://europepmc.org/articles/PMC4569427?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
You Li David Rabern Simmons Craig C Bateman Dylan P G Short Matthew T Kasson Robert J Rabaglia Jiri Hulcr |
spellingShingle |
You Li David Rabern Simmons Craig C Bateman Dylan P G Short Matthew T Kasson Robert J Rabaglia Jiri Hulcr New Fungus-Insect Symbiosis: Culturing, Molecular, and Histological Methods Determine Saprophytic Polyporales Mutualists of Ambrosiodmus Ambrosia Beetles. PLoS ONE |
author_facet |
You Li David Rabern Simmons Craig C Bateman Dylan P G Short Matthew T Kasson Robert J Rabaglia Jiri Hulcr |
author_sort |
You Li |
title |
New Fungus-Insect Symbiosis: Culturing, Molecular, and Histological Methods Determine Saprophytic Polyporales Mutualists of Ambrosiodmus Ambrosia Beetles. |
title_short |
New Fungus-Insect Symbiosis: Culturing, Molecular, and Histological Methods Determine Saprophytic Polyporales Mutualists of Ambrosiodmus Ambrosia Beetles. |
title_full |
New Fungus-Insect Symbiosis: Culturing, Molecular, and Histological Methods Determine Saprophytic Polyporales Mutualists of Ambrosiodmus Ambrosia Beetles. |
title_fullStr |
New Fungus-Insect Symbiosis: Culturing, Molecular, and Histological Methods Determine Saprophytic Polyporales Mutualists of Ambrosiodmus Ambrosia Beetles. |
title_full_unstemmed |
New Fungus-Insect Symbiosis: Culturing, Molecular, and Histological Methods Determine Saprophytic Polyporales Mutualists of Ambrosiodmus Ambrosia Beetles. |
title_sort |
new fungus-insect symbiosis: culturing, molecular, and histological methods determine saprophytic polyporales mutualists of ambrosiodmus ambrosia beetles. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2015-01-01 |
description |
Ambrosia symbiosis is an obligate, farming-like mutualism between wood-boring beetles and fungi. It evolved at least 11 times and includes many notorious invasive pests. All ambrosia beetles studied to date cultivate ascomycotan fungi: early colonizers of recently killed trees with poor wood digestion. Beetles in the widespread genus Ambrosiodmus, however, colonize decayed wood. We characterized the mycosymbionts of three Ambrosiodmus species using quantitative culturing, high-throughput metabarcoding, and histology. We determined the fungi to be within the Polyporales, closely related to Flavodon flavus. Culture-independent sequencing of Ambrosiodmus minor mycangia revealed a single operational taxonomic unit identical to the sequences from the cultured Flavodon. Histological sectioning confirmed that Ambrosiodmus possessed preoral mycangia containing dimitic hyphae similar to cultured F. cf. flavus. The Ambrosiodmus-Flavodon symbiosis is unique in several aspects: it is the first reported association between an ambrosia beetle and a basidiomycotan fungus; the mycosymbiont grows as hyphae in the mycangia, not as budding pseudo-mycelium; and the mycosymbiont is a white-rot saprophyte rather than an early colonizer: a previously undocumented wood borer niche. Few fungi are capable of turning rotten wood into complete animal nutrition. Several thousand beetle-fungus symbioses remain unstudied and promise unknown and unexpected mycological diversity and enzymatic innovations. |
url |
http://europepmc.org/articles/PMC4569427?pdf=render |
work_keys_str_mv |
AT youli newfungusinsectsymbiosisculturingmolecularandhistologicalmethodsdeterminesaprophyticpolyporalesmutualistsofambrosiodmusambrosiabeetles AT davidrabernsimmons newfungusinsectsymbiosisculturingmolecularandhistologicalmethodsdeterminesaprophyticpolyporalesmutualistsofambrosiodmusambrosiabeetles AT craigcbateman newfungusinsectsymbiosisculturingmolecularandhistologicalmethodsdeterminesaprophyticpolyporalesmutualistsofambrosiodmusambrosiabeetles AT dylanpgshort newfungusinsectsymbiosisculturingmolecularandhistologicalmethodsdeterminesaprophyticpolyporalesmutualistsofambrosiodmusambrosiabeetles AT matthewtkasson newfungusinsectsymbiosisculturingmolecularandhistologicalmethodsdeterminesaprophyticpolyporalesmutualistsofambrosiodmusambrosiabeetles AT robertjrabaglia newfungusinsectsymbiosisculturingmolecularandhistologicalmethodsdeterminesaprophyticpolyporalesmutualistsofambrosiodmusambrosiabeetles AT jirihulcr newfungusinsectsymbiosisculturingmolecularandhistologicalmethodsdeterminesaprophyticpolyporalesmutualistsofambrosiodmusambrosiabeetles |
_version_ |
1725115002268942336 |