Dendroctonus (Genus)
Related Symbionts
53 recordsSymbiont records associated with Dendroctonus genus
Classification | Host | Function | Function Tags | Reference | |
---|---|---|---|---|---|
Pseudomonas sp. 7 B321
Pseudomonadota |
Bacteria
|
volatiles from predominant bacteria regulate the consumption sequence of carbon sources d-pinitol and d-glucose in the fungal symbiont Leptographium … |
- | ||
Rahnella aquatilis B3None1
Pseudomonadota |
Bacteria
|
volatiles from predominant bacteria regulate the consumption sequence of carbon sources d-pinitol and d-glucose in the fungal symbiont Leptographium … |
- | ||
Serratia liquefaciens B31None
Pseudomonadota |
Bacteria
|
volatiles from predominant bacteria regulate the consumption sequence of carbon sources d-pinitol and d-glucose in the fungal symbiont Leptographium … |
- | ||
Leptographium procerum
Ascomycota |
Fungi
|
enhances the survivorship and overall fitness of invasive beetles by degrading the host phenolic naringenin, ultimately overcoming the tree defenses … |
Plant secondary metabolites
|
||
Burkholderia
Pseudomonadota |
Bacteria
|
It can trongly degrade naringenin, and pinitol, the main soluble carbohydrate of P. tabuliformis, is retained in L. procerum-infected phloem and faci… |
Digestive enzymes
|
||
Novosphingobium
Pseudomonadota |
Bacteria
|
It can trongly degrade naringenin, and pinitol, the main soluble carbohydrate of P. tabuliformis, is retained in L. procerum-infected phloem and faci… |
Digestive enzymes
|
||
Rhodotorula
Basidiomycota |
Fungi
|
It can trongly degrade naringenin, and pinitol, the main soluble carbohydrate of P. tabuliformis, is retained in L. procerum-infected phloem and faci… |
Digestive enzymes
|
||
Grosmannia clavigera
Ascomycota |
Fungi
|
Grosmannia clavigera can detoxify oleoresin terpenoids (conifer-defence chemicals) and utilize them as carbon sources. It allows host insects to tole… |
Plant secondary metabolites
|
||
Leptographium procerum CMW25626
Ascomycota |
Fungi
|
consumption of one common carbon source d-glucose over another carbohydrate d-pinitol in pine phloem tissues by the fungus inhibit D. valens larval w… |
Growth and Development
|
||
Grosmannia clavigera
Ascomycota |
Fungi
|
The symbiotic fungus can utilize terpenes as carbon sources. Genes involved in terpene-degradation were expressed in symbionts cultured with plant ma… |
Digestive enzymes
|
||
Leptographium abietinum
Ascomycota |
Fungi
|
inoculation with L. abietinum significantly reduced concentrations of a tree defensive compound, (+)-4-carene, in growth media |
Plant secondary metabolites
|
||
Leptographium abietinum
Ascomycota |
Fungi
|
inoculation with L. abietinum significantly reduced concentrations of a tree defensive compound, (+)-3-carene, in growth media |
Plant secondary metabolites
|
||
Grosmannia clavigera
Ascomycota |
Fungi
|
Increased success of host insect on jack pines (host plant) reduces food quality for interspecific competitors |
- | ||
Grosmannia clavigera
Ascomycota |
Fungi
|
fungal pathogenicity likely is more important in aiding MPB colonization and development within the host tree |
- | ||
Pseudomonas
Pseudomonadota |
Bacteria
|
could alleviate or compromise the antagonistic effects of fungi O. minus and L. procerum on RTB larval growth |
Growth and Development
Immune priming
|
||
Rahnella aquatilis
Pseudomonadota |
Bacteria
|
could alleviate or compromise the antagonistic effects of fungi O. minus and L. procerum on RTB larval growth |
Growth and Development
Immune priming
|
||
Serratia liquefaciens
Pseudomonadota |
Bacteria
|
could alleviate or compromise the antagonistic effects of fungi O. minus and L. procerum on RTB larval growth |
Growth and Development
Immune priming
|
||
Grosmannia clavigera
Ascomycota |
Fungi
|
Oxygenated monoterpenes produced by microbial activity is used as host (beetle) location cues by parasitoids |
- | ||
Rahnella aquatilis
Pseudomonadota |
Bacteria
|
R. aquatilis decreased (−)-α-pinene (38%) and (+)-α-pinene (46%) by 40% and 45% (by GC-MS), respectively |
Plant secondary metabolites
|
||
Serratia proteamaculans
Pseudomonadota |
Bacteria
|
display strong cellulolytic activity and process a single endoglucanase encoding gene |
Digestive enzymes
|
||
Burkholderia
Pseudomonadota |
Bacteria
|
Genera contained most genes involved in terpene degradation (by metagenomics) |
Plant secondary metabolites
|
||
Pseudomonas
Pseudomonadota |
Bacteria
|
Genera contained most genes involved in terpene degradation (by metagenomics) |
Plant secondary metabolites
|
||
Rahnella
Pseudomonadota |
Bacteria
|
Genera contained most genes involved in terpene degradation (by metagenomics) |
Plant secondary metabolites
|
||
Serratia
Pseudomonadota |
Bacteria
|
Genera contained most genes involved in terpene degradation (by metagenomics) |
Plant secondary metabolites
|
||
Ophiostoma minus
Ascomycota |
Fungi
|
The phenoloxidase ratio increased significantly in the larvae with O. minus |
Immune priming
|
||
Cyberlindnera americana ChDrAdgY46
Ascomycota |
Fungi
|
play a role in the detoxification process of tree defensive chemicals |
Plant secondary metabolites
|
||
Leptographium procerum
Ascomycota |
Fungi
|
Inducing host pines to produce 3-carene, an attractant of the beetle |
Chemical biosynthesis
|
||
Pseudomonas mandelii
Pseudomonadota |
Bacteria
|
P. mandelii decreased concentrations of all monoterpenes by 15–24% |
Plant secondary metabolites
|
||
Streptomyces
Actinomycetota |
Bacteria
|
Defense against antagonistic fungus of the beetle's cultivar |
Antimicrobials
|
||
Serritia marcescens
Pseudomonadota |
Bacteria
|
S. marcescens reduced 49–79% of 3-carene and (−)-β-pinene |
Plant secondary metabolites
|
||
Rahnella
Pseudomonadota |
Bacteria
|
It may specialize in terpenoid metabolism. |
Plant secondary metabolites
|
||
Serratia
Pseudomonadota |
Bacteria
|
It may specialize in terpenoid metabolism. |
Plant secondary metabolites
|
||
Leptographium procerum
Ascomycota |
Fungi
|
compete with RTB larvae for carbohydrates |
- | ||
Ophiostoma minus
Ascomycota |
Fungi
|
compete with RTB larvae for carbohydrates |
- | ||
Pseudomonas sp,
Pseudomonadota |
Bacteria
|
Degraded 20–50% of α-pinene (by GC-MS) |
Plant secondary metabolites
|
||
Rahnella aquatilis
Pseudomonadota |
Bacteria
|
Degraded 20–50% of α-pinene (by GC-MS) |
Plant secondary metabolites
|
||
Serratia sp.
Pseudomonadota |
Bacteria
|
Degraded 20–50% of α-pinene (by GC-MS) |
Plant secondary metabolites
|
||
bacteria
- |
Bacteria
|
- |
- | ||
Endoconidiophora
Ascomycota |
Fungi
|
- |
- | ||
Bacteria
|
- |
- | |||
Grosmannia clavigera
Ascomycota |
Fungi
|
- |
- | ||
Grosmannia clavigera
Ascomycota |
Fungi
|
- |
- | ||
Bacteria
|
- |
- | |||
Leptographium procerum
Ascomycota |
Fungi
|
- |
- | ||
Leptographium sanjiangyuanense sp. nov.
Ascomycota |
Fungi
|
- |
- | ||
Leptographium zekuense sp. nov.
Ascomycota |
Fungi
|
- |
- | ||
Ophiostoma huangnanense sp. nov.
Ascomycota |
Fungi
|
- |
- | ||
Ophiostoma maixiuense sp. nov.
Ascomycota |
Fungi
|
- |
- | ||
Ophiostoma montium
Ascomycota |
Fungi
|
- |
- | ||
Ophiostoma sanum sp. nov.
Ascomycota |
Fungi
|
- |
- | ||
Ophiostoma sp.
Ascomycota |
Fungi
|
- |
- | ||
Rahnella
Pseudomonadota |
Bacteria
|
- |
- | ||
Spiroplasma
Mycoplasmatota |
Bacteria
|
- |
- |
Metagenome Information
0 recordsMetagenome sequencing data associated with Dendroctonus species
Run | Platform | Host | Location | Date | BioProject |
---|---|---|---|---|---|
No metagenomes foundNo metagenome records associated with Dendroctonus species. |
Amplicon Information
0 recordsAmplicon sequencing data associated with Dendroctonus species
Run | Classification | Host | Platform | Location | Environment |
---|---|---|---|---|---|
No amplicons foundNo amplicon records associated with Dendroctonus species. |