Investigating the effects of symbiotic fungi on the flight behaviour ofSirex noctilio(Hymenoptera: Siricidae)

2016 ◽  
Vol 148 (5) ◽  
pp. 543-551 ◽  
Author(s):  
Mark A. Sarvary ◽  
Ann E. Hajek ◽  
Katalin Böröczky ◽  
Robert A. Raguso ◽  
Miriam F. Cooperband

AbstractThe invasive woodwaspSirex noctilioFabricius (Hymenoptera: Siricidae) is obligately associated with the symbiotic white rot fungusAmylostereum areolatum(Chaillet ex Fries) Boidin (Basidiomycota: Amylosteraceae), and shows positive chemotaxis to volatiles emitted by this symbiont. After introduction to North America,S. noctiliowas collected carrying another fungus speciesAmylostereum chailletii(Persoon) Boidin, used symbiotically by native North AmericanSirexLinnaeus. We conducted flight behaviour studies in a walk-in flight tunnel to evaluate specificity of the attraction of mated and unmatedS. noctilioto its primary symbiont,A. areolatum, versus the alternative symbiont,A. chailletii. Fewer unmated than matedS. noctiliofemales responded to either of the fungi. Unmated females showed no landing preference but matedS. noctiliofemales were attracted toA. areolatumalthough avoidance ofA. chailletiiwas not complete. Chemical analysis demonstrated major differences in the volatile profiles of the two fungal species. Sesquiterpenes dominated theA. areolatumsamples, whereas only two aromatic volatiles were consistently present in the nativeA. chailletii.

2018 ◽  
Vol 19 (8) ◽  
pp. 2379 ◽  
Author(s):  
Young-Jin Park ◽  
Yong-Un Jeong ◽  
Won-Sik Kong

Next-generation sequencing (NGS) of the Flammulina elastica (wood-rotting basidiomycete) genome was performed to identify carbohydrate-active enzymes (CAZymes). The resulting assembly (31 kmer) revealed a total length of 35,045,521 bp (49.7% GC content). Using the AUGUSTUS tool, 12,536 total gene structures were predicted by ab initio gene prediction. An analysis of orthologs revealed that 6806 groups contained at least one F. elastica protein. Among the 12,536 predicted genes, F. elastica contained 24 species-specific genes, of which 17 genes were paralogous. CAZymes are divided into five classes: glycoside hydrolases (GHs), carbohydrate esterases (CEs), polysaccharide lyases (PLs), glycosyltransferases (GTs), and auxiliary activities (AA). In the present study, annotation of the predicted amino acid sequences from F. elastica genes using the dbCAN CAZyme database revealed 508 CAZymes, including 82 AAs, 218 GHs, 89 GTs, 18 PLs, 59 CEs, and 42 carbohydrate binding modules in the F. elastica genome. Although the CAZyme repertoire of F. elastica was similar to those of other fungal species, the total number of GTs in F. elastica was larger than those of other basidiomycetes. This genome information elucidates newly identified wood-degrading machinery in F. elastica, offers opportunities to better understand this fungus, and presents possibilities for more detailed studies on lignocellulosic biomass degradation that may lead to future biotechnological and industrial applications.


2021 ◽  
Vol 7 (4) ◽  
pp. 265
Author(s):  
Junko Sugano ◽  
Ndegwa Maina ◽  
Janne Wallenius ◽  
Kristiina Hildén

Wood decomposition is a sophisticated process where various biocatalysts act simultaneously and synergistically on biopolymers to efficiently break down plant cell walls. In nature, this process depends on the activities of the wood-inhabiting fungal communities that co-exist and interact during wood decay. Wood-decaying fungal species have traditionally been classified as white-rot and brown-rot fungi, which differ in their decay mechanism and enzyme repertoire. To mimic the species interaction during wood decomposition, we have cultivated the white-rot fungus, Bjerkandera adusta, and two brown-rot fungi, Gloeophyllum sepiarium and Antrodia sinuosa, in single and co-cultivations on softwood and hardwood. We compared their extracellular hydrolytic carbohydrate-active and oxidative lignin-degrading enzyme activities and production profiles. The interaction of white-rot and brown-rot species showed enhanced (hemi)cellulase activities on birch and spruce-supplemented cultivations. Based on the enzyme activity profiles, the combination of B. adusta and G. sepiarium facilitated birch wood degradation, whereas B. adusta and A. sinuosa is a promising combination for efficient degradation of spruce wood, showing synergy in β-glucosidase (BGL) and α-galactosidase (AGL) activity. Synergistic BGL and AGL activity was also detected on birch during the interaction of brown-rot species. Our findings indicate that fungal interaction on different woody substrates have an impact on both simultaneous and sequential biocatalytic activities.


NeoBiota ◽  
2019 ◽  
Vol 44 ◽  
pp. 39-55
Author(s):  
Tonya D. Bittner ◽  
Nathan Havill ◽  
Isis A.L. Caetano ◽  
Ann E. Hajek

Sirexnoctilio is an invasive woodwasp that, along with its symbiotic fungus, has killed pine trees (Pinus spp.) in North America and in numerous countries in the Southern Hemisphere. We tested a biological control agent in North America that has successfully controlled S.noctilio in Oceania, South Africa, and South America. Deladenussiricidicola nematodes feed on the symbiotic white rot fungus Amylostereumareolatum and can switch to being parasitic on S.noctilio. When parasitic, the Kamona nematode strain can sterilise the eggs of S.noctilio females. However, in North America, a different strain of D.siricidicola (NA), presumably introduced along with the woodwasp, parasitises but does not sterilise S.noctilio. We tested the sterilising Kamona biological control strain of D.siricidicola against S.noctilio in North America. Interactions between the biological control strain and the NA strain could include competitive exclusion, co-infection within hosts or hybridisation. We reared D.siricidicola Kamona on an A.areolatum strain native to North America (IGS-BE) and another strain (IGS-BDF) used commercially to mass-produce the nematode in Australia. We inoculated Kamona reared on either strain of A.areolatum into logs infested with S.noctilio larvae and compared parasitism rates against control logs. Individual nematodes were isolated from S.noctilio hemocoels and from sterilised eggs and were genotyped with eight microsatellite loci. A high rate of parasitisation of S.noctilio by D.siricidicolaNA was found for all treatments and we found evidence of both co-infection and hybridisation. Surprisingly, sterilisation rates were not related to the rates of parasitisation by D.siricidicola Kamona.


2020 ◽  
Vol 7 (6) ◽  
pp. 246-274
Author(s):  
Ayodele A Otaiku ◽  
AI Alhaji

A major limitation of the white-rot fungus is its sensitivity during biodegradation of mixed matrix explosive pollutants and the scale of Kachia military shooting since 1967, Nigeria. The amplified 16S rRNA gene of each microbial isolate was processed for sequencing and characterization with Gene Bank database. Fungal species heavy metal reduction in increasing order of Aspergillus niger > Trametes versicolor > Rhizopus spp > Phanorochate chrysoporium > Penicillium spp were identified. The total explosive contents shows a significant difference for all locations in both dry and wet seasons (P<0.05) using Anova test. Microbial fungi consortium (MFC) bioremediate heavy metal significantly at 61.7% relative to isolated fungi species because of the lateral gene transfer/co-metabolism, where Trametes versicolor and Aspergillus niger act as gene mediators. MFC growth in 1% mineral salt medium munitions was significance than fungal species isolate. Deploying Myco Bio-augmentation / Phytoremediation/Biosimulation (Myco B-P-B) techniques to optimize the RDX and HMX characterized by a higher Nitrogen/Carbon ratio since fungi lack the beta-glucuronidase (GUS) gene to utilize carbon source directly. Pollutants bio-stimulation will enhances co-metabolism by MFC. Plant detoxification capabilities can be improved using fungi genes laccases and cytochrome P450 monooxygenase expressed effectively in plants using protoplast fusion


Plant Disease ◽  
2008 ◽  
Vol 92 (7) ◽  
pp. 1138-1138 ◽  
Author(s):  
M.-J. Bergeron ◽  
R. C. Hamelin ◽  
I. Leal ◽  
C. Davis ◽  
P. de Groot

Amylostereum areolatum (Fr.) Boidin (Russulales: Stereaceae) is a white rot fungus that has a symbiotic relationship with several woodwasps including Sirex noctilio Fabricius (Hymenoptera: Siricidae). The vectored fungus together with a phytotoxic mucus, both injected during oviposition by the female S. noctilio, rapidly weaken the host tree, rendering it susceptible to larval development (3). Host trees of A. areolatum include species of Pinus (mainly), Abies, Larix, and Picea and Cryptomeria japonica and Pseudotsuga menziesii (Fungal Databases [online]; USDA). The siricid woodwasp is native to Eurasia and North Africa and has been introduced into New Zealand, Australia, South America, and South Africa (1). In July of 2005, the first established North American population of S. noctilio was reported in Oswego, NY. Prompted by this initial discovery, a trap survey of Ontario counties located along the Canada-U.S. border, close to Upstate New York, was conducted in September and October of 2005. S. noctilio females were captured in four locations in southern Ontario. Two additional locations for S. noctilio were also reported in a survey conducted independently (2). In September and October of 2006, logs of Scots pines showing current Sirex oviposition sites were harvested from the Ontario area bordered by Lakes Huron, Erie, and Ontario to determine the presence of the species-specific fungal symbiont of S. noctilio, A. areolatum. Fungal isolates were obtained by surface sterilizing wood chips showing decay columns followed by incubation at 20°C on 2% malt extract agar. Cultures with morphological characteristics typical of A. areolatum–presence of clamp connections and arthrospores–were used for DNA analysis to confirm species identification. DNA sequences of the internal transcribed spacer (ITS) of the ribosomal RNA gene were queried against the NCBI GenBank database. There was a 99 to 100% match between the ITS sequences from the Ontario isolates and sequences from European and Asian A. areolatum isolates (GenBank Accession Nos. EU249343 and EU249344 versus AF454428, AF506405, AY781245, and AF218389). Matches with A. chailletii (Pers.) Boidin, a native related species, were around 97%. These results confirmed the presence of A. areolatum in the infested material. Cultures were deposited in the National Mycological Herbarium of Canada (DAOM 239280–DAOM 239295). To our knowledge, this represents the first report of A. areolatum in Canada. In its natural range, the insect-fungal complex exists in equilibrium with its host trees and parasites, thus, few negative impacts are observed. However, in the Southern Hemisphere where it has been introduced, it has become a major pest, attacking many important commercial North American species planted as exotics (1). Conifer forests in Canada are threatened by the spread of the S. noctilio/A. areolatum complex, particularly plantations and stands of Pinus banksiana, P. contorta, P. ponderosa, P. resinosa, P. strobus, and P. sylvestris. A survey of Eastern Canada to detect the presence of S. noctilio is on going, and genetics work is being conducted to determine the origin of the introduction of A. areolatum. References: (1) W. M. Ciesla. J. For. 101:18, 2003. (2) P. de Groot et al. Gt. Lakes Entomol. 39:49, 2006. (3) B. Slippers et al. S. Afr. J. Sci. 99:70, 2003.


2020 ◽  
Vol 18 (1) ◽  
pp. 135-145
Author(s):  
Vu Dinh Giap ◽  
Thai Thi My Hiep ◽  
Do Huu Nghi

       Fungal enzymes are well-known as effective in hydrolyze lignocellulose-rich materials. This decomposition process requires many enzymes to participate in a coordinated factor to hydrolyze the polymer structure. Among them, there are some of popular oxidized enzymes such as lignin peroxidase, mangan peroxidase and laccase. Cellobiose dehydrogenase (CDH) is an extracellular enzyme found in various fungi, it was first discovered in 1974 by Westermark in white rot fungus Trametes verscolor and Phanerochaete chrysosporium. The biological role of CDH has been proven to participate in the decomposition of natural polymers such as cellulose, hemicellulose and lignin by generating hydroxyl radical through Fenton reaction. CDH has unique biochemical and catalytic properties that have been used in biosensors to detect cellodextrin, maltose, lactose and diphenol compounds or in biomedical applications such as lactobionic acid production. Therefore, CDH is an important component of the extracellular enzyme system for lignocellulose decomposition.  In this study, 47 fungal strains isolated from rainforests of Cuc Phuong and Muong Phang National Parks and screened for CDH activity. Of which, 33 active fungi exhibited CDH activity from 8.89 to 74.4 U/L during growth on solid medium with rice straw as raw substrate. The highest enzyme production was identified for Coprinellus aureogranulatus (MPG14) reach 77.4 U/L on basic medium and its CDH activity of up to 237.4 U/L under optimal condition: supplemented with carbon source of α- cellulose (20 g/L), nitrogen source (5 g/L peptone) incubated for 12 days at 30℃, pH 5.5 and 200 rpm after inoculation.     Thus, the fungus has the potential to exploit the CDH enzyme applied in the pretreatment of lignocellulose-rich materials.    


2012 ◽  
Vol 3 (1) ◽  
pp. 20-21
Author(s):  
A.Sangeetha A.Sangeetha ◽  
◽  
K.Thanigai K.Thanigai ◽  
Narasimhamurthy Narasimhamurthy ◽  
S.K.Nath S.K.Nath

2020 ◽  
Vol 93 (9) ◽  
pp. 289-292
Author(s):  
Yumi SHIMIZU ◽  
Shuma SATHO ◽  
Taro NAKAJIMA ◽  
Hiroaki KOUZAI ◽  
Kiminori SHIMIZU

2018 ◽  
Vol 69 (1) ◽  
pp. 38-44
Author(s):  
Nicoleta Mirela Marin ◽  
Olga Tiron ◽  
Luoana Florentina Pascu ◽  
Mihaela Costache ◽  
Mihai Nita Lazar ◽  
...  

This study investigates the synergistic effects of ion exchange and biodegradation methods to remove the Acid Blue 193 also called Gryfalan Navy Blue RL (GNB) dye from wastewater. Ion exchange studies were performed using a strongly basic anion exchange resin Amberlite IRA 400. The equilibrium was characterized by a kinetic and thermodynamic points of view, establishing that the sorption of the GNB dye was subject to the Freundlich isotherm model with R2 = 0.8710. Experimental results showed that the activated resin can removed up to 93.4% when the concentration of dye solution is 5.62�10-2 mM. The biodegradation of the GNB was induced by laccase, an enzyme isolated from white-rot fungus. It was also analyzed the role of pH and dye concentration on GNB biodegradation, so 5�10-2 mM dye had a maximum discoloration efficiency of 82.9% at pH of 4. The laccase showed a very fast and robust activity reaching in a few minutes a Km value of 2.2�10-1mM. In addition, increasing the GNB concentration up to 8�10-1 mM did not triggered a substrat inhibition effect on the laccase activity. Overall, in this study we proposed a mixt physicochemical and biological approach to enhance the GNB removal and biodegradability from the wastewaters and subsequently the environment.


1991 ◽  
Vol 24 (3-4) ◽  
pp. 189-198 ◽  
Author(s):  
V. P. Lankinen ◽  
M. M. Inkeröinen ◽  
J. Pellinen ◽  
A. I. Hatakka

Decrease of adsorbable organic chlorine (AOX) is becoming the most important criterion for the efficiency of pulp mill effluent treatment in the 1990s. Two methods, designated MYCOR and MYCOPOR which utilize the white-rot fungus Phanerochaete chrysosporium have earlier been developed for the color removal of pulp mill effluents, but the processes have also a capacity to decrease the amount of chlorinated organic compounds. Lignin peroxidases (ligninases) produced by P. chrvsosporium may dechlorinate chlorinated phenols. In this work possibilities to use selected white-rot fungi in the treatment of E1-stage bleach plant effluent were studied. Phlebia radiata. Phanerochaete chrvsosporium and Merulius (Phlebia) tremellosus were compared in shake flasks for their ability to produce laccase, lignin peroxidase(s) and manganese-dependent peroxidase(s) and to remove color from a medium containing effluent. Softwood bleaching effluents were treated by carrier-immobilized P. radiata in 2 1 bioreactors and a 10 1 BiostatR -fermentor. Dechlorination was followed using Cl ion and AOX determinations. All fungi removed the color of the effluent. In P. radiata cultivations AOX decrease was ca. 4 mg l−1 in one day. Apparent lignin peroxidase activities as determined by veratryl alcohol oxidation method were negligible or zero in a medium with AOX content of ca. 60 mg l−1, prepared using about 20 % (v/v) of softwood effluent. However, the purification of extracellular enzymes implied that large amounts of lignin peroxidases were present in the medium and, after the purification, in active form. Enzyme proteins were separated using anion exchange chromatography, and they were further characterized by electrophoresis (SDS-PAGE) to reveal the kind of enzymes that were present during AOX decrease and color removal. The most characteristic lignin peroxidase isoenzymes in effluent media were LiP2 and LiP3.


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