Blattodea (Order)
Related Symbionts
101 recordsSymbiont records associated with Blattodea order
Classification | Host | Function | Function Tags | Reference | |
---|---|---|---|---|---|
Stenotrophomonas
Pseudomonadota |
Bacteria
|
Stenotrophomonas spp. can colonize a gut microbiome with limited other symbionts in the presence of kanamycin.The antibiotic-induced dysbiosis and insecticide tolerance that occurred in the resistant strain suggest new, exciting mutualistic relationships between gut microbiota and their insect hosts. |
Nutrient provision
Antimicrobials
Fungal farming
|
||
Bacillus cereus F837/76
Bacillota |
Bacteria
|
The ability of these arthropods to feed on wood, foliage and detritus is likely to involve catalysis by different types of cellulases/hemicellulases that are secreted by gut microbiota to digest the structural and recalcitrant lignocellulosic residues in their foods. |
Digestive enzymes
|
||
Bacillus cereus TAUC5
Bacillota |
Bacteria
|
The ability of these arthropods to feed on wood, foliage and detritus is likely to involve catalysis by different types of cellulases/hemicellulases that are secreted by gut microbiota to digest the structural and recalcitrant lignocellulosic residues in their foods. |
Digestive enzymes
|
||
Bacillus licheniformis ACO1
Bacillota |
Bacteria
|
The ability of these arthropods to feed on wood, foliage and detritus is likely to involve catalysis by different types of cellulases/hemicellulases that are secreted by gut microbiota to digest the structural and recalcitrant lignocellulosic residues in their foods. |
Digestive enzymes
|
||
Bacillus licheniformis BCRC 15413
Bacillota |
Bacteria
|
The ability of these arthropods to feed on wood, foliage and detritus is likely to involve catalysis by different types of cellulases/hemicellulases that are secreted by gut microbiota to digest the structural and recalcitrant lignocellulosic residues in their foods. |
Digestive enzymes
|
||
Bacillus licheniformis EdyKolBl23
Bacillota |
Bacteria
|
The ability of these arthropods to feed on wood, foliage and detritus is likely to involve catalysis by different types of cellulases/hemicellulases that are secreted by gut microbiota to digest the structural and recalcitrant lignocellulosic residues in their foods. |
Digestive enzymes
|
||
Bacillus licheniformis SubaMucBl16
Bacillota |
Bacteria
|
The ability of these arthropods to feed on wood, foliage and detritus is likely to involve catalysis by different types of cellulases/hemicellulases that are secreted by gut microbiota to digest the structural and recalcitrant lignocellulosic residues in their foods. |
Digestive enzymes
|
||
Bacillus pumilus BSH4
Bacillota |
Bacteria
|
The ability of these arthropods to feed on wood, foliage and detritus is likely to involve catalysis by different types of cellulases/hemicellulases that are secreted by gut microbiota to digest the structural and recalcitrant lignocellulosic residues in their foods. |
Digestive enzymes
|
||
Bacillus sp. 6None63
Bacillota |
Bacteria
|
The ability of these arthropods to feed on wood, foliage and detritus is likely to involve catalysis by different types of cellulases/hemicellulases that are secreted by gut microbiota to digest the structural and recalcitrant lignocellulosic residues in their foods. |
Digestive enzymes
|
||
Bacillus sp. DV9-35
Bacillota |
Bacteria
|
The ability of these arthropods to feed on wood, foliage and detritus is likely to involve catalysis by different types of cellulases/hemicellulases that are secreted by gut microbiota to digest the structural and recalcitrant lignocellulosic residues in their foods. |
Digestive enzymes
|
||
Bacillus sp. SCSSS1None
Bacillota |
Bacteria
|
The ability of these arthropods to feed on wood, foliage and detritus is likely to involve catalysis by different types of cellulases/hemicellulases that are secreted by gut microbiota to digest the structural and recalcitrant lignocellulosic residues in their foods. |
Digestive enzymes
|
||
Bacillus subtilis K21
Bacillota |
Bacteria
|
The ability of these arthropods to feed on wood, foliage and detritus is likely to involve catalysis by different types of cellulases/hemicellulases that are secreted by gut microbiota to digest the structural and recalcitrant lignocellulosic residues in their foods. |
Digestive enzymes
|
||
Bacillus subtilis M5None
Bacillota |
Bacteria
|
The ability of these arthropods to feed on wood, foliage and detritus is likely to involve catalysis by different types of cellulases/hemicellulases that are secreted by gut microbiota to digest the structural and recalcitrant lignocellulosic residues in their foods. |
Digestive enzymes
|
||
Klebsiella sp. clone F7
Pseudomonadota |
Bacteria
|
The ability of these arthropods to feed on wood, foliage and detritus is likely to involve catalysis by different types of cellulases/hemicellulases that are secreted by gut microbiota to digest the structural and recalcitrant lignocellulosic residues in their foods. |
Digestive enzymes
|
||
Paenibacillus polymyxa DSM 36T
Bacillota |
Bacteria
|
The ability of these arthropods to feed on wood, foliage and detritus is likely to involve catalysis by different types of cellulases/hemicellulases that are secreted by gut microbiota to digest the structural and recalcitrant lignocellulosic residues in their foods. |
Digestive enzymes
|
||
Pantoea agglomerans WAB1927
Pseudomonadota |
Bacteria
|
The ability of these arthropods to feed on wood, foliage and detritus is likely to involve catalysis by different types of cellulases/hemicellulases that are secreted by gut microbiota to digest the structural and recalcitrant lignocellulosic residues in their foods. |
Digestive enzymes
|
||
Trabulsiella guamensis GTC1379
Pseudomonadota |
Bacteria
|
The ability of these arthropods to feed on wood, foliage and detritus is likely to involve catalysis by different types of cellulases/hemicellulases that are secreted by gut microbiota to digest the structural and recalcitrant lignocellulosic residues in their foods. |
Digestive enzymes
|
||
Trabulsiella guamensis GTC1379
Pseudomonadota |
Bacteria
|
The ability of these arthropods to feed on wood, foliage and detritus is likely to involve catalysis by different types of cellulases/hemicellulases that are secreted by gut microbiota to digest the structural and recalcitrant lignocellulosic residues in their foods. |
Digestive enzymes
|
||
Treponema azotonutricium (ZAS-9)
Spirochaetota |
Bacteria
|
when grown together, two termite-gut Treponema species influence each other's gene expression in a far more comprehensive and nuanced manner than might have been predicted based on the results of previous studies on the respective pure cultures |
- | ||
Treponema primitia (ZAS-2)
Spirochaetota |
Bacteria
|
when grown together, two termite-gut Treponema species influence each other's gene expression in a far more comprehensive and nuanced manner than might have been predicted based on the results of previous studies on the respective pure cultures |
- | ||
Neonectria discophora
Ascomycota |
Fungi
|
it can produce chlorinated metabolites of the ilicicolin and azaphilone families, which have biological properties such as anticancer, antiviral, antibacterial, anti-inflammatory, antifungal, antifouling and insecticidal activity. |
Chemical biosynthesis
|
||
Penicillium sclerotiorum
Ascomycota |
Fungi
|
it can produce chlorinated metabolites of the ilicicolin and azaphilone families, which have biological properties such as anticancer, antiviral, antibacterial, anti-inflammatory, antifungal, antifouling and insecticidal activity. |
Chemical biosynthesis
|
||
Bacteria
|
gut microbiota is not essential in this species for survival and development throughout its complete life cycle, but it could participate in complementation of host nutrition by helping with food digestion and nutrient absorption |
Nutrient provision
Digestive enzymes
|
|||
Bacteria and Fungi
|
harbor a broad set of genes or gene modules encoding carbohydrate-active enzymes (CAZymes) relevant to plant fiber degradation, particularly debranching enzymes and oligosaccharide-processing enzymes |
Digestive enzymes
|
|||
Acinetobacter pittii
Pseudomonadota |
Bacteria
|
gut microbiota contributes to production of VCAs that act as fecal aggregation agents and that cockroaches discriminate among the complex odors that emanate from a diverse microbial community |
- | ||
Acinetobacter sp.
Pseudomonadota |
Bacteria
|
gut microbiota contributes to production of VCAs that act as fecal aggregation agents and that cockroaches discriminate among the complex odors that emanate from a diverse microbial community |
- | ||
Enterococcus avium
Bacillota |
Bacteria
|
gut microbiota contributes to production of VCAs that act as fecal aggregation agents and that cockroaches discriminate among the complex odors that emanate from a diverse microbial community |
- | ||
Pseudomonas japonica
Pseudomonadota |
Bacteria
|
gut microbiota contributes to production of VCAs that act as fecal aggregation agents and that cockroaches discriminate among the complex odors that emanate from a diverse microbial community |
- | ||
Pseudomonas monteilii
Pseudomonadota |
Bacteria
|
gut microbiota contributes to production of VCAs that act as fecal aggregation agents and that cockroaches discriminate among the complex odors that emanate from a diverse microbial community |
- | ||
Weissella cibaria
Bacillota |
Bacteria
|
gut microbiota contributes to production of VCAs that act as fecal aggregation agents and that cockroaches discriminate among the complex odors that emanate from a diverse microbial community |
- | ||
Blattabacterium cuenoti
Bacteroidota |
Bacteria
|
enables hosts to subsist on a nutrient-poor diet; endosymbiont genome erosions are associated with repeated host transitions to an underground life |
Nutrient provision
|
||
Aequitasia blattaphilus
Bacillota |
Bacteria
|
its genomes encoded short-chain fatty acid biosynthetic pathways and plant fiber and chitin catabolism and other carbohydrate utilization genes |
Digestive enzymes
|
||
Ohessyouella blattaphilus
Bacillota |
Bacteria
|
its genomes encoded short-chain fatty acid biosynthetic pathways and plant fiber and chitin catabolism and other carbohydrate utilization genes |
Digestive enzymes
|
||
Blattabacterium str. BPLAN
Bacteroidota |
Bacteria
|
can recycle nitrogen from urea and ammonia, which are uric acid degradation products, into glutamate, using urease and glutamate dehydrogenase |
Nitrogen fixation
|
||
Pseudallescheria boydii
Ascomycota |
Fungi
|
produces ovalicin derivatives resulting from the esterification of the less hindered site of the ovalicin epoxide by long-chain fatty acids |
Chemical biosynthesis
|
||
Blattabacterium
Bacteroidota |
Bacteria
|
Blattabacterium endosymbionts could directly or indirectly influence the composition of other bacterial populations by reducing diversity |
- | ||
Pseudomonas
Pseudomonadota |
Bacteria
|
can function as a defensive mutualist as it prevents the weedy fungus while keeping the crop fungus (fungus garden) unaffected |
Fungal farming
Antimicrobials
|
||
Bacteria and Fungi
|
thrives on recalcitrant lignocellulosic diets through nutritional symbioses with gut-dwelling prokaryotes and eukaryotes |
Digestive enzymes
|
|||
Nephridiophaga javanicae
Nephridiophagidae |
Fungi
|
They infect the Malpighian tubules where especially the lumen can be densely colonised by different life cycle stages |
- | ||
Nephridiophaga postici
Nephridiophagidae |
Fungi
|
They infect the Malpighian tubules where especially the lumen can be densely colonised by different life cycle stages |
- | ||
Termitomyces
Basidiomycota |
Fungi
|
produce several known drimanes and drimenol-type sesquiterpenoids, which are C15 bicyclic sesquiterpenes |
Chemical biosynthesis
|
||
Blattabacterium strain Bge
Bacteroidota |
Bacteria
|
codes for the complete urea cycle that, in combination with urease, produces ammonia as an end product |
Nitrogen fixation
|
||
Athelia termitophila
Basidiomycota |
Fungi
|
may enhance egg survival probably due to the synthesis of antifungal and antibacterial compounds |
Antimicrobials
|
||
Lachnospira
Bacillota |
Bacteria
|
Hydrolyze polysaccharide; assist digestion; synthesize acetate, propionate, and butyrate |
Sugar metabolism
Digestive enzymes
|
||
Pseudomonas reactans
Pseudomonadota |
Bacteria
|
Secrete versatile secondary metabolites; provide protection from parasites and pathogens |
Natural enemy resistance
|
||
Blattabacterium sp.
Bacteroidota |
Bacteria
|
involved in uric acid degradation, nitrogen assimilation and nutrient provisioning |
Nitrogen fixation
Nutrient provision
|
||
Blattabacterium sp.
Bacteroidota |
Bacteria
|
involved in uric acid degradation, nitrogen assimilation and nutrient provisioning |
Nitrogen fixation
Nutrient provision
|
||
Streptococcus
Bacillota |
Bacteria
|
can be broken down into substances such as carbon dioxide, ammonia and acetic acid |
Digestive enzymes
|
||
Bacillus licheniformis
Bacillota |
Bacteria
|
process termiticidal activity of chitinase enzyme from gut symbiont isolate |
Digestive enzymes
|
||
Blochmannia
Pseudomonadota |
Bacteria
|
produce ammonia from dietary urea and then use it as a source of nitrogen |
Nitrogen fixation
|
||
Blattabacterium
Bacteroidota |
Bacteria
|
use nitrogenous wastes in essential amino acid and vitamin biosynthesis |
Nitrogen fixation
Nutrient provision
|
||
Serratia marcescens
Pseudomonadota |
Bacteria
|
high concentration of S. marcescens leads to high mortality in termites |
- | ||
Isaria fumosorosea K3
Ascomycota |
Fungi
|
Affecting direction of motion by providing 3-octanone and 1-octen-3-ol |
- | ||
Bacteria
|
implicated in xylan, the major component of hemicellulose degradation |
Digestive enzymes
|
|||
fiber-associated bacteria
Spirochaetota |
Bacteria
|
implicated in xylan, the major component of hemicellulose degradation |
Digestive enzymes
|
||
Bacteria and Fungi
|
gut symbionts are major recyclers of lignocellulosic biomass |
Digestive enzymes
|
|||
Blattabacterium
Bacteroidota |
Bacteria
|
contribute to freeze-tolerance of the insect hosts |
- | ||
Fusarium spp.
Ascomycota |
Fungi
|
contribute to freeze-tolerance of the insect hosts |
- | ||
Mortierella spp.
Mucoromycota |
Fungi
|
contribute to freeze-tolerance of the insect hosts |
- | ||
Pseudomonas fluorescens
Pseudomonadota |
Bacteria
|
contribute to freeze-tolerance of the insect hosts |
- | ||
Bacillus cereus
Bacillota |
Bacteria
|
isolates showed significant cellulolytic activity |
Digestive enzymes
|
||
Lysinibacillus fusiformis
Bacillota |
Bacteria
|
isolates showed significant cellulolytic activity |
Digestive enzymes
|
||
Lysinibacillus macrolides
Bacillota |
Bacteria
|
isolates showed significant cellulolytic activity |
Digestive enzymes
|
||
Paenibacillus lactis
Bacillota |
Bacteria
|
isolates showed significant cellulolytic activity |
Digestive enzymes
|
||
Stenotrophomonas maltophilia
Pseudomonadota |
Bacteria
|
isolates showed significant cellulolytic activity |
Digestive enzymes
|
||
Termitomyces
Basidiomycota |
Fungi
|
rely on gut symbionts to decompose organic matter |
Digestive enzymes
|
||
Bacteria
|
highly efficient digestion of lignocellulose |
Digestive enzymes
|
|||
Wolbachia
Pseudomonadota |
Bacteria
|
induces reproductive incompatibility |
Reproductive manipulation
|
||
Blattabacterium cuenoti
Bacteroidota |
Bacteria
|
collaborative arginine biosynthesis |
Nutrient provision
|
||
Blattabacterium cuenoti
Bacteroidota |
Bacteria
|
collaborative arginine biosynthesis |
Nutrient provision
|
||
Pseudomonas syringae
Pseudomonadota |
Bacteria
|
initiate crystallization of water |
- | ||
Bacteroides
Bacteroidota |
Bacteria
|
has the ability to degrade urate |
Digestive enzymes
|
||
Salmonella spp.
Pseudomonadota |
Bacteria
|
Increase the host drug resistant |
Pesticide metabolization
|
||
Salmonella spp.
Pseudomonadota |
Bacteria
|
Increase the host drug resistant |
Pesticide metabolization
|
||
Enterobacter sp. ydwj-5
Pseudomonadota |
Bacteria
|
phenol-degrading bacteria |
Plant secondary metabolites
|
||
Blattabacterium cuenoti
Bacteroidota |
Bacteria
|
obligate endosymbiont |
- | ||
Bacteria
|
digest lignocellulose |
Digestive enzymes
|
|||
Buchnera
Pseudomonadota |
Bacteria
|
supply nutrient |
Nutrient provision
|
||
Bacteria and Fungi
|
gut microbiome |
- | |||
bacteria
- |
Bacteria
|
- |
- | ||
Blattabacterium
Bacteroidota |
Bacteria
|
- |
- | ||
Blattabacterium cuenoti
Bacteroidota |
Bacteria
|
- |
- | ||
Devescovina aymara n. sp.
Parabasalia |
Bacteria
|
- |
- | ||
Devescovina sapara n. sp.
Parabasalia |
Bacteria
|
- |
- | ||
Ereboglobus luteus
Verrucomicrobiota |
Bacteria
|
- |
- | ||
Bacteria
|
- |
- | |||
Bacteria
|
- |
- | |||
Bacteria
|
- |
- | |||
Metschnikowia ahupensis f.a., sp. nov.
Ascomycota |
Fungi
|
- |
- | ||
Pantoea agglomerans
Pseudomonadota |
Bacteria
|
- |
- | ||
Pantoea vagans
Pseudomonadota |
Bacteria
|
- |
- | ||
Pseudacidobacterium ailaaui
Acidobacteriota |
Bacteria
|
- |
- | ||
Pseudocitrobacter corydidari sp. nov.
Pseudomonadota |
Bacteria
|
- |
- | ||
Rhizobiaceae
Pseudomonadota |
Bacteria
|
- |
- | ||
Runanympha illapa n. sp.
Parabasalia |
Bacteria
|
- |
- | ||
Runanympha pacha n. sp.
Parabasalia |
Bacteria
|
- |
- | ||
Bacteria and Fungi
|
- |
- | |||
Terracidiphilus gabretensis
Acidobacteriota |
Bacteria
|
- |
- | ||
Treponema
Spirochaetota |
Bacteria
|
- |
- | ||
Wolbachia
Pseudomonadota |
Bacteria
|
- |
- | ||
Wolbachia
Pseudomonadota |
Bacteria
|
- |
- |
Metagenome Information
4 recordsMetagenome sequencing data associated with Blattodea order
Run | Platform | Host | Location | Date | BioProject |
---|---|---|---|---|---|
SRR333074
WGS |
LS454
454 GS FLX |
-
|
Mar-24
|
PRJNA70279 | |
SRR333075
WGS |
LS454
454 GS FLX |
-
|
Mar-24
|
PRJNA70279 | |
DRR019499
WGS |
ILLUMINA
Illumina HiSeq 2000 |
Japan
24.34 N 123.91 E |
2011-10-09
|
PRJDB1602 | |
DRR021338
WGS |
ILLUMINA
Illumina HiSeq 2000 |
Japan
36.21 N 140.10 E |
2011-10-01
|
PRJDB477 |
Amplicon Information
252 recordsAmplicon sequencing data associated with Blattodea order
Run | Classification | Host | Platform | Location | Environment |
---|---|---|---|---|---|
DRR182924
AMPLICON |
16S
|
-
|
South Korea
missing |
insect-associated habitat
intestinal |
|
DRR182922
AMPLICON |
16S
|
-
|
Japan
missing |
insect-associated habitat
intestinal |
|
DRR182921
AMPLICON |
16S
|
-
|
Malaysia
missing |
insect-associated habitat
intestinal |
|
DRR182919
AMPLICON |
16S
|
-
|
Japan
missing |
insect-associated habitat
intestinal |
|
DRR182918
AMPLICON |
16S
|
-
|
Thailand
missing |
insect-associated habitat
intestinal |
|
DRR182916
AMPLICON |
16S
|
-
|
Australia
missing |
insect-associated habitat
intestinal |
|
DRR182960
AMPLICON |
16S
|
-
|
Japan
missing |
insect-associated habitat
intestinal |
|
DRR182959
AMPLICON |
16S
|
-
|
Japan
missing |
insect-associated habitat
intestinal |
|
DRR182958
AMPLICON |
16S
|
-
|
Japan
missing |
insect-associated habitat
intestinal |
|
DRR182957
AMPLICON |
16S
|
-
|
Japan
missing |
insect-associated habitat
intestinal |
|
DRR182955
AMPLICON |
16S
|
-
|
Australia
missing |
insect-associated habitat
intestinal |
|
DRR182954
AMPLICON |
16S
|
-
|
Taiwan
missing |
insect-associated habitat
intestinal |
|
DRR182953
AMPLICON |
16S
|
-
|
Japan
missing |
insect-associated habitat
intestinal |
|
DRR182952
AMPLICON |
16S
|
-
|
Malaysia
missing |
insect-associated habitat
intestinal |
|
DRR182951
AMPLICON |
16S
|
-
|
Malaysia
missing |
insect-associated habitat
intestinal |
|
DRR182948
AMPLICON |
16S
|
-
|
Malaysia
missing |
insect-associated habitat
intestinal |
|
DRR182947
AMPLICON |
16S
|
-
|
Thailand
missing |
insect-associated habitat
intestinal |
|
DRR182946
AMPLICON |
16S
|
-
|
Australia
missing |
insect-associated habitat
intestinal |
|
DRR182945
AMPLICON |
16S
|
-
|
Malaysia
missing |
insect-associated habitat
intestinal |
|
DRR182944
AMPLICON |
16S
|
-
|
Thailand
missing |
insect-associated habitat
intestinal |
|
DRR182943
AMPLICON |
16S
|
-
|
Australia
missing |
insect-associated habitat
intestinal |
|
DRR182942
AMPLICON |
16S
|
-
|
Malaysia
missing |
insect-associated habitat
intestinal |
|
DRR182938
AMPLICON |
16S
|
-
|
Malaysia
missing |
insect-associated habitat
intestinal |
|
DRR182937
AMPLICON |
16S
|
-
|
Malaysia
missing |
insect-associated habitat
intestinal |
|
DRR182935
AMPLICON |
16S
|
-
|
Japan
missing |
insect-associated habitat
intestinal |
|
DRR182934
AMPLICON |
16S
|
-
|
Malaysia
missing |
insect-associated habitat
intestinal |
|
DRR182932
AMPLICON |
16S
|
-
|
Japan
missing |
insect-associated habitat
intestinal |
|
DRR182931
AMPLICON |
16S
|
-
|
Japan
missing |
insect-associated habitat
intestinal |
|
DRR182930
AMPLICON |
16S
|
-
|
Malaysia
missing |
insect-associated habitat
intestinal |
|
DRR182929
AMPLICON |
16S
|
-
|
Australia
missing |
insect-associated habitat
intestinal |
|
DRR182928
AMPLICON |
16S
|
-
|
Malaysia
missing |
insect-associated habitat
intestinal |
|
DRR182927
AMPLICON |
16S
|
-
|
Malaysia
missing |
insect-associated habitat
intestinal |
|
DRR182926
AMPLICON |
16S
|
-
|
USA
missing |
insect-associated habitat
intestinal |
|
DRR182925
AMPLICON |
16S
|
-
|
USA
missing |
insect-associated habitat
intestinal |
|
DRR182923
AMPLICON |
16S
|
-
|
USA
missing |
insect-associated habitat
intestinal |
|
DRR182997
AMPLICON |
16S
|
-
|
Japan
missing |
insect-associated habitat
intestinal |
|
DRR182996
AMPLICON |
16S
|
-
|
Malaysia
missing |
insect-associated habitat
intestinal |
|
DRR182995
AMPLICON |
16S
|
-
|
Thailand
missing |
insect-associated habitat
intestinal |
|
DRR182994
AMPLICON |
16S
|
-
|
Malaysia
missing |
insect-associated habitat
intestinal |
|
DRR182993
AMPLICON |
16S
|
-
|
Malaysia
missing |
insect-associated habitat
intestinal |
|
DRR182992
AMPLICON |
16S
|
-
|
Thailand
missing |
insect-associated habitat
intestinal |
|
DRR182990
AMPLICON |
16S
|
-
|
Australia
missing |
insect-associated habitat
intestinal |
|
DRR182988
AMPLICON |
16S
|
-
|
Japan
missing |
insect-associated habitat
intestinal |
|
DRR182986
AMPLICON |
16S
|
-
|
Malaysia
missing |
insect-associated habitat
intestinal |
|
DRR182985
AMPLICON |
16S
|
-
|
Thailand
missing |
insect-associated habitat
intestinal |
|
DRR182983
AMPLICON |
16S
|
-
|
Japan
missing |
insect-associated habitat
intestinal |
|
DRR182982
AMPLICON |
16S
|
-
|
Taiwan
missing |
insect-associated habitat
intestinal |
|
DRR182981
AMPLICON |
16S
|
-
|
Japan
missing |
insect-associated habitat
intestinal |
|
DRR182979
AMPLICON |
16S
|
-
|
Japan
missing |
insect-associated habitat
intestinal |
|
DRR182978
AMPLICON |
16S
|
-
|
Japan
missing |
insect-associated habitat
intestinal |
|
DRR182977
AMPLICON |
16S
|
-
|
Taiwan
missing |
insect-associated habitat
intestinal |
|
DRR182975
AMPLICON |
16S
|
-
|
Malaysia
missing |
insect-associated habitat
intestinal |
|
DRR182974
AMPLICON |
16S
|
-
|
Malaysia
missing |
insect-associated habitat
intestinal |
|
DRR182973
AMPLICON |
16S
|
-
|
Malaysia
missing |
insect-associated habitat
intestinal |
|
DRR182971
AMPLICON |
16S
|
-
|
Australia
missing |
insect-associated habitat
intestinal |
|
DRR182970
AMPLICON |
16S
|
-
|
Japan
missing |
insect-associated habitat
intestinal |
|
DRR182969
AMPLICON |
16S
|
-
|
Japan
missing |
insect-associated habitat
intestinal |
|
DRR182968
AMPLICON |
16S
|
-
|
Japan
missing |
insect-associated habitat
intestinal |
|
DRR182967
AMPLICON |
16S
|
-
|
Malaysia
missing |
insect-associated habitat
intestinal |
|
DRR182965
AMPLICON |
16S
|
-
|
Malaysia
missing |
insect-associated habitat
intestinal |
|
DRR182964
AMPLICON |
16S
|
-
|
Malaysia
missing |
insect-associated habitat
intestinal |
|
DRR182963
AMPLICON |
16S
|
-
|
Japan
missing |
insect-associated habitat
intestinal |
|
DRR182962
AMPLICON |
16S
|
-
|
Malaysia
missing |
insect-associated habitat
intestinal |
|
DRR182961
AMPLICON |
16S
|
-
|
Japan
missing |
insect-associated habitat
intestinal |
|
SRR2035362
AMPLICON |
16S
|
-
|
Brazil
missing |
-
|
|
SRR2035371
AMPLICON |
16S
|
-
|
USA
missing |
-
|
|
SRR6837977
RNA-Seq |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR6837976
RNA-Seq |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR6837975
RNA-Seq |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR6837972
RNA-Seq |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR6837971
RNA-Seq |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR6837970
RNA-Seq |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR7226439
AMPLICON |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR7226424
AMPLICON |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR7226441
AMPLICON |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR7226442
AMPLICON |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR7226443
AMPLICON |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR7226444
AMPLICON |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR6837981
RNA-Seq |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR7226425
AMPLICON |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR7226434
AMPLICON |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR7226448
AMPLICON |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR7226449
AMPLICON |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR7226451
AMPLICON |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR7226430
AMPLICON |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR7226453
AMPLICON |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR7226454
AMPLICON |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR7226456
AMPLICON |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR7226459
AMPLICON |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR7226437
AMPLICON |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR7226438
AMPLICON |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR7226445
AMPLICON |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR6837979
RNA-Seq |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR7226421
AMPLICON |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR7226422
AMPLICON |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR7226423
AMPLICON |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR7226428
AMPLICON |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR7226429
AMPLICON |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR7226432
AMPLICON |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR7226433
AMPLICON |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR7226435
AMPLICON |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR7226440
AMPLICON |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR7226446
AMPLICON |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR7226447
AMPLICON |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR7226452
AMPLICON |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR7226460
AMPLICON |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR7226461
AMPLICON |
16S
|
-
|
French Guiana
missing |
-
|
|
SRR11604158
AMPLICON |
16S
|
-
|
China
23.5 N 113 E |
-
|
|
SRR11604163
AMPLICON |
16S
|
-
|
China
23.5 N 113 E |
-
|
|
SRR11604162
AMPLICON |
16S
|
-
|
China
23.5 N 113 E |
-
|
|
SRR11604161
AMPLICON |
16S
|
-
|
China
23.5 N 113 E |
-
|
|
SRR11604160
AMPLICON |
16S
|
-
|
China
23.5 N 113 E |
-
|
|
SRR11604159
AMPLICON |
16S
|
-
|
China
23.5 N 113 E |
-
|
|
SRR19147674
AMPLICON |
16S
|
-
|
Germany
50.5697 N 8.6729 E |
Insect-associated microbiome
Insect-associated gut microbiome |
|
SRR19147663
AMPLICON |
16S
|
-
|
Germany
50.5697 N 8.6729 E |
Insect-associated microbiome
Insect-associated gut microbiome |
|
SRR19147664
AMPLICON |
16S
|
-
|
Germany
50.5697 N 8.6729 E |
Insect-associated microbiome
Insect-associated gut microbiome |
|
SRR19147665
AMPLICON |
16S
|
-
|
Germany
50.5697 N 8.6729 E |
Insect-associated microbiome
Insect-associated gut microbiome |
|
SRR19147666
AMPLICON |
16S
|
-
|
Germany
50.5697 N 8.6729 E |
Insect-associated microbiome
Insect-associated gut microbiome |
|
SRR19147667
AMPLICON |
16S
|
-
|
Germany
50.5697 N 8.6729 E |
Insect-associated microbiome
Insect-associated gut microbiome |
|
SRR19147668
AMPLICON |
16S
|
-
|
Germany
50.5697 N 8.6729 E |
Insect-associated microbiome
Insect-associated gut microbiome |
|
SRR19147669
AMPLICON |
16S
|
-
|
Germany
50.5697 N 8.6729 E |
Insect-associated microbiome
Insect-associated gut microbiome |
|
SRR19147670
AMPLICON |
16S
|
-
|
Germany
50.5697 N 8.6729 E |
Insect-associated microbiome
Insect-associated gut microbiome |
|
SRR19147671
AMPLICON |
16S
|
-
|
Germany
50.5697 N 8.6729 E |
Insect-associated microbiome
Insect-associated gut microbiome |
|
SRR19147672
AMPLICON |
16S
|
-
|
Germany
50.5697 N 8.6729 E |
Insect-associated microbiome
Insect-associated gut microbiome |
|
SRR19147673
AMPLICON |
16S
|
-
|
Germany
50.5697 N 8.6729 E |
Insect-associated microbiome
Insect-associated gut microbiome |
|
SRR19147675
AMPLICON |
16S
|
-
|
Germany
50.5697 N 8.6729 E |
Insect-associated microbiome
Insect-associated gut microbiome |
|
SRR19147676
AMPLICON |
16S
|
-
|
Germany
50.5697 N 8.6729 E |
Insect-associated microbiome
Insect-associated gut microbiome |
|
SRR19147677
AMPLICON |
16S
|
-
|
Germany
50.5697 N 8.6729 E |
Insect-associated microbiome
Insect-associated gut microbiome |
|
SRR21660797
AMPLICON |
16S
|
-
|
Senegal
14.0667 N 16.5833 W |
-
|
|
SRR8893845
AMPLICON |
16S
|
-
|
China
missing |
-
|
|
SRR8893849
AMPLICON |
16S
|
-
|
China
missing |
-
|
|
SRR8893837
AMPLICON |
16S
|
-
|
China
missing |
-
|
|
SRR8893833
AMPLICON |
16S
|
-
|
China
missing |
-
|
|
SRR8893836
AMPLICON |
16S
|
-
|
China
missing |
-
|
|
SRR8893835
AMPLICON |
16S
|
-
|
China
missing |
-
|
|
SRR8893834
AMPLICON |
16S
|
-
|
China
missing |
-
|
|
SRR8893840
AMPLICON |
16S
|
-
|
China
missing |
-
|
|
SRR8893839
AMPLICON |
16S
|
-
|
China
missing |
-
|
|
SRR8893841
AMPLICON |
16S
|
-
|
China
missing |
-
|
|
SRR8893842
AMPLICON |
16S
|
-
|
China
missing |
-
|
|
SRR8893838
AMPLICON |
16S
|
-
|
China
missing |
-
|
|
SRR8893843
AMPLICON |
16S
|
-
|
China
missing |
-
|
|
SRR8893844
AMPLICON |
16S
|
-
|
China
missing |
-
|
|
SRR8893846
AMPLICON |
16S
|
-
|
China
missing |
-
|
|
SRR8893847
AMPLICON |
16S
|
-
|
China
missing |
-
|
|
SRR8893848
AMPLICON |
16S
|
-
|
China
missing |
-
|
|
SRR8893826
AMPLICON |
16S
|
-
|
China
missing |
-
|
|
SRR8893827
AMPLICON |
16S
|
-
|
China
missing |
-
|
|
SRR8893828
AMPLICON |
16S
|
-
|
China
missing |
-
|
|
SRR8893829
AMPLICON |
16S
|
-
|
China
missing |
-
|
|
SRR8893830
AMPLICON |
16S
|
-
|
China
missing |
-
|
|
SRR8893831
AMPLICON |
16S
|
-
|
China
missing |
-
|
|
SRR8893832
AMPLICON |
16S
|
-
|
China
missing |
-
|
|
SRR6306522
AMPLICON |
16S
|
-
|
China
21.55 N 101.15 E |
-
|
|
SRR6306521
AMPLICON |
16S
|
-
|
China
21.55 N 101.15 E |
-
|
|
SRR3521315
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521314
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521313
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521312
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521311
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521310
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521309
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521308
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521307
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521306
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521305
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521304
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521303
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521302
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521301
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521300
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521299
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521298
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521297
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521296
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521295
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521294
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521293
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521339
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521290
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521289
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521287
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521286
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521285
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521283
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521281
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521280
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521278
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521277
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521276
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521275
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521273
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521272
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521271
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521268
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521267
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521266
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521265
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521264
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521263
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521262
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521261
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521260
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521258
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521291
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521340
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521341
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521342
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521343
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521344
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521345
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521346
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521347
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521348
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521349
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521350
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521351
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521352
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521353
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521354
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521355
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521356
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521357
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521358
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521359
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521360
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521361
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521362
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521363
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521338
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521337
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521336
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521335
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521334
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521333
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521332
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521331
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521330
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521329
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521328
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521327
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521326
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521325
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521324
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521323
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521322
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521321
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521320
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521319
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521318
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521317
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|
|
SRR3521316
AMPLICON |
16S
|
-
|
uncalculated
not collected |
-
|