SRR5342619 - Hippodamia convergens
Basic Information
Run: SRR5342619
Assay Type: WGS
Bioproject: PRJNA377711
Biosample: SAMN25047086
Bytes: 704687117
Center Name: EMBRAPA
Sequencing Information
Instrument: Illumina HiSeq 2500
Library Layout: PAIRED
Library Selection: RANDOM
Platform: ILLUMINA
Geographic Information
Country: Brazil
Continent: South America
Location Name: Brazil: Distrito Federal
Latitude/Longitude: 15.73 S 47.9002 W
Sample Information
Host: Hippodamia convergens
Isolation: -
Biosample Model: Metagenome or environmental
Collection Date: 2015
Taxonomic Classification
Potential Symbionts
About Potential Symbionts
This table shows potential symbiont identified in the metagenome sample. Matches are scored based on:
- Relative abundance in the sample
- Species-level matches with known symbionts
- Host insect order matches with reference records
- Completeness and richness of functional records
Based on our current records database, this section aims to identify potential functional symbionts in this metagenome sample, with scoring based on:
- Relative abundance in sample
- Species-level matches with known symbionts
- Host insect order matches
- Functional record completeness
Note: Showing top 3 highest scoring records for each species/genus
Symbiont Name | Record | Host Species | Function | Abundance |
Score
Score Composition:
Higher scores indicate stronger symbiotic relationship potential |
---|---|---|---|---|---|
Pseudomonas sp. CIP-10
Species-level Match
Host Order Match
|
RISB1622 |
Dendroctonus valens
Order: Coleoptera
|
volatiles from predominant bacteria regulate the consumption sequence of carbon sources d-pinitol and d-glucose in the fungal symbiont Leptographium procerum, and appear to alleviate the antagonistic effect from the fungus against RTB larvae
|
2.20% |
22.0
|
Pseudomonas sp. CIP-10
Species-level Match
Host Order Match
|
RISB2224 |
Leptinotarsa decemlineata
Order: Coleoptera
|
Colorado potato beetle (Leptinotarsa decemlineata) larvae exploit bacteria in their oral secretions to suppress antiherbivore defenses in tomato (Solanum lycopersicum)
|
2.20% |
20.5
|
Bacillus cereus
Species-level Match
Host Order Match
|
RISB1056 |
Oryctes rhinoceros
Order: Coleoptera
|
provide symbiotic digestive functions to Oryctes
|
4.20% |
20.2
|
Bacillus cereus
Species-level Match
Host Order Match
|
RISB1778 |
Lissorhoptrus oryzophilus
Order: Coleoptera
|
might be promising paratransgenesis candidates
|
4.20% |
20.1
|
Lactococcus lactis
Species-level Match
Host Order Match
|
RISB0967 |
Oulema melanopus
Order: Coleoptera
|
contribute to the decomposition of complex carbohydrates, fatty acids, or polysaccharides in the insect gut. It might also contribute to the improvement of nutrient availability.
|
0.72% |
19.3
|
Escherichia coli
Species-level Match
Host Order Match
|
RISB0128 |
Tribolium castaneum
Order: Coleoptera
|
may produce 4,8-dimethyldecanal (DMD) production that is strongly associated with attraction to females and host pheromone communication
|
1.42% |
19.1
|
Sphingobacterium sp. R2
Species-level Match
Host Order Match
|
RISB2227 |
Leptinotarsa decemlineata
Order: Coleoptera
|
Colorado potato beetle (Leptinotarsa decemlineata) larvae exploit bacteria in their oral secretions to suppress antiherbivore defenses in tomato (Solanum lycopersicum)
|
0.38% |
18.7
|
Pseudomonas sp. CIP-10
Species-level Match
Host Order Match
|
RISB0815 |
Hypothenemus hampei
Order: Coleoptera
|
might contribute to caffeine breakdown using the C-15 oxidation pathway
|
2.20% |
18.6
|
Streptomyces sp. T12
Species-level Match
Host Order Match
|
RISB0777 |
Copris tripartitus
Order: Coleoptera
|
contribute brood ball hygiene by inhibiting fungal parasites in the environment
|
1.22% |
17.8
|
Lactococcus lactis
Species-level Match
Host Order Match
|
RISB1430 |
Rhynchophorus ferrugineus
Order: Coleoptera
|
promote the development and body mass gain of RPW larvae by improving their nutrition metabolism
|
0.72% |
17.6
|
Wolbachia
Host Order Match
|
RISB1452 |
Octodonta nipae
Order: Coleoptera
|
Wolbachia harbored dominantly in a female than the male adult, while, no significant differences were observed between male and female body parts and tissues
|
4.50% |
17.6
|
Serratia marcescens
Species-level Match
Host Order Match
|
RISB1295 |
Nicrophorus vespilloides
Order: Coleoptera
|
producing antibacterial compound Serrawettin W2, which has antibacterial and nematode-inhibiting effects
|
0.42% |
17.5
|
Serratia marcescens
Species-level Match
Host Order Match
|
RISB0365 |
Pagiophloeus tsushimanus
Order: Coleoptera
|
terpenoid-degrading: the highest degradation rates of D-camphor, linalool, and eucalyptol
|
0.42% |
17.2
|
Wolbachia
Host Order Match
|
RISB2107 |
Sitophilus zeamais
Order: Coleoptera
|
Wolbachia directly favored weevil fertility and exhibited only mild indirect effects, usually enhancing the SZPE effect
|
4.50% |
16.9
|
Stenotrophomonas maltophilia
Species-level Match
Host Order Match
|
RISB0139 |
Tenebrio molitor
Order: Coleoptera
|
correlated with polyvinyl chloride PVC degradation
|
0.88% |
16.9
|
Klebsiella pneumoniae
Species-level Match
Host Order Match
|
RISB1153 |
Tenebrio molitor
Order: Coleoptera
|
degrading plastics
|
1.47% |
16.8
|
Serratia marcescens
Species-level Match
Host Order Match
|
RISB1158 |
Nicrophorus vespilloides
Order: Coleoptera
|
produces an antibacterial cyclic lipopeptide called serrawettin W2
|
0.42% |
16.7
|
Wolbachia
Host Order Match
|
RISB1282 |
Ips sp.
Order: Coleoptera
|
inducing cytoplasmic incompatibility, resulting in reproductive distortions and hence
|
4.50% |
16.2
|
Lactococcus lactis
Species-level Match
Host Order Match
|
RISB1065 |
Oryctes rhinoceros
Order: Coleoptera
|
gut microbe
|
0.72% |
15.9
|
Acinetobacter
Host Order Match
|
RISB0730 |
Curculio chinensis
Order: Coleoptera
|
Acinetobacter sp. in C. chinensis enriched after treating with saponin, and when incubating bacteria with saponin for 72 h, saponin content significantly decreased from 4.054 to 1.867 mg/mL (by 16S rRNA metagenome sequencing and HPLC)
|
1.03% |
15.7
|
Staphylococcus epidermidis
Species-level Match
Host Order Match
|
RISB1070 |
Oryctes rhinoceros
Order: Coleoptera
|
gut microbe
|
0.20% |
15.4
|
Vibrio
Host Order Match
|
RISB1810 |
Monochamus galloprovincialis
Order: Coleoptera
|
Have the ability for degradation of cellulose, proteins and starch
|
3.18% |
14.5
|
Acinetobacter
Host Order Match
|
RISB1356 |
Callosobruchus maculatus
Order: Coleoptera
|
These bacterial phyla may allow the adults C. maculatus to survive on DDVP treated grains, thereby making it inappropriate to control the beetle populations in the field.
|
1.03% |
14.4
|
Bacillus cereus
Species-level Match
|
RISB2161 |
Termitidae
Order: Blattodea
|
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.
|
4.20% |
14.2
|
Proteus
Host Order Match
|
RISB0001 |
Leptinotarsa decemlineata
Order: Coleoptera
|
produces toxic hydrogen cyanide (HCN) and a mandelonitrile-producing cyanoglucoside, amygdalin, which protect the insect from predation
|
1.21% |
13.9
|
Spiroplasma
Host Order Match
|
RISB0343 |
Harmonia axyridis
Order: Coleoptera
|
female ladybirds co-infected with Hesperomyces harmoniae and Spiroplasma had a significantly lower fecundity and hatchability compared to females with only one or no symbiont
|
0.40% |
13.9
|
Buchnera aphidicola
Species-level Match
|
RISB0236 |
Acyrthosiphon pisum
Order: Hemiptera
|
Buchnera the nutritional endosymbiont of A. pisum is located inside of bacteriocytes and requires aspartate from the aphid host, because it cannot make it de novo. Further Buchnera needs aspartate for the biosynthesis of the essential amino acids lysine and threonine, which the aphid and Buchnera require for survival
|
3.61% |
13.6
|
Buchnera aphidicola
Species-level Match
|
RISB2485 |
Macrosiphum euphorbiae
Order: Hemiptera
|
symbiont expression patterns differ between aphid clones with differing levels of virulence, and are influenced by the aphids' host plant. Potentially, symbionts may contribute to differential adaptation of aphids to host plant resistance
|
3.61% |
13.4
|
Acinetobacter
Host Order Match
|
RISB0520 |
Leptinotarsa decemlineata
Order: Coleoptera
|
inhibited the expression of genes associated with the JA-mediated defense signaling pathway and SGA biosynthesis
|
1.03% |
13.3
|
Spiroplasma
Host Order Match
|
RISB1483 |
Brachinus elongatulus
Order: Coleoptera
|
may manipulate host reproduction (e.g., cause male-killing) or provide resistance to nematodes and/or parasitoid wasps
|
0.40% |
12.8
|
Bacteroides
Host Order Match
|
RISB1183 |
Oryzaephilus surinamensis
Order: Coleoptera
|
supplement precursors for the cuticle synthesis and thereby enhance desiccation resistance of its host
|
0.64% |
12.7
|
Clostridium
|
RISB2301 |
Pyrrhocoris apterus
Order: Hemiptera
|
could play an important role for the insect by degrading complex dietary components, providing nutrient supplementation, or detoxifying noxious chemicals (e.g. cyclopropenoic fatty acids or gossypol) in the diet
|
8.23% |
12.5
|
Buchnera aphidicola
Species-level Match
|
RISB0685 |
Acyrthosiphon pisum
Order: Hemiptera
|
It supplies the host with vitamins and essential amino acids, such as arginine and methionine that aphids cannot synthesize or derive insufficiently from their diet, the phloem sap of plants
|
3.61% |
12.4
|
Leuconostoc
Host Order Match
|
RISB0812 |
Hypothenemus hampei
Order: Coleoptera
|
might contribute to caffeine breakdown using the C-18 oxidation pathway
|
0.37% |
11.8
|
Nostoc
Host Order Match
|
RISB0812 |
Hypothenemus hampei
Order: Coleoptera
|
might contribute to caffeine breakdown using the C-18 oxidation pathway
|
0.28% |
11.7
|
Klebsiella pneumoniae
Species-level Match
|
RISB2185 |
Scirpophaga incertulas
Order: Lepidoptera
|
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.
|
1.47% |
11.5
|
Lysinibacillus
Host Order Match
|
RISB1066 |
Oryctes rhinoceros
Order: Coleoptera
|
gut microbe
|
1.08% |
11.3
|
Spiroplasma
Host Order Match
|
RISB0250 |
Tenebrio molitor
Order: Coleoptera
|
associated with PE biodegradation
|
0.40% |
11.1
|
Exiguobacterium
Host Order Match
|
RISB1152 |
Tenebrio molitor
Order: Coleoptera
|
degrading plastics
|
0.53% |
10.9
|
Escherichia coli
Species-level Match
|
RISB1339 |
Manduca sexta
Order: Lepidoptera
|
modulate immunity-related gene expression in the infected F0 larvae, and also in their offspring, triggered immune responses in the infected host associated with shifts in both DNA methylation and histone acetylation
|
1.42% |
10.7
|
Paenibacillus polymyxa
Species-level Match
|
RISB2195 |
Termitidae
Order: Blattodea
|
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.
|
0.50% |
10.5
|
Streptomyces sp. T12
Species-level Match
|
RISB0943 |
Polybia plebeja
Order: Hymenoptera
|
this bacterium produces antimicrobial compounds that are active against Hirsutella citriformis, a natural fungal enemy of its host, and the human pathogens Staphylococcus aureus and Candida albicans
|
1.22% |
10.2
|
Streptomyces sp. T12
Species-level Match
|
RISB2334 |
Sirex noctilio
Order: Hymenoptera
|
degrading woody substrates and that such degradation may assist in nutrient acquisition by S. noctilio, thus contributing to its ability to be established in forested habitats worldwide
|
1.22% |
9.9
|
Stenotrophomonas maltophilia
Species-level Match
|
RISB1122 |
Bombyx mori
Order: Lepidoptera
|
facilitate host resistance against organophosphate insecticides, provides essential amino acids that increase host fitness and allow the larvae to better tolerate the toxic effects of the insecticide.
|
0.88% |
9.9
|
Clostridium
|
RISB0028 |
Sesamia inferens
Order: Lepidoptera
|
degrade Chlorpyrifos and Chlorantraniliprole in vitro
|
8.23% |
9.3
|
Mammaliicoccus sciuri
Species-level Match
|
RISB0075 |
Bombyx mori
Order: Lepidoptera
|
could produce a secreted chitinolytic lysozyme (termed Msp1) to damage fungal cell walls,completely inhibit the spore germination of fungal entomopathogens Metarhizium robertsii and Beauveria bassiana
|
0.24% |
9.2
|
Blattabacterium cuenoti
Species-level Match
|
RISB0133 |
Panesthiinae
Order: Blattodea
|
enables hosts to subsist on a nutrient-poor diet; endosymbiont genome erosions are associated with repeated host transitions to an underground life
|
0.98% |
8.9
|
Stenotrophomonas maltophilia
Species-level Match
|
RISB1227 |
Delia antiqua
Order: Diptera
|
six bacteria protect larvae from infection with the entomopathogen Beauveria bassiana through symbiotic bacterium-derived organic acids
|
0.88% |
8.6
|
Enterococcus casseliflavus
Species-level Match
|
RISB0112 |
Bactrocera dorsalis
Order: Diptera
|
increase the resistance of B. dorsalis to β-cypermethrin by regulating cytochrome P450 (P450) enzymes and α-glutathione S-transferase (GST) activities
|
0.43% |
8.4
|
Clostridium
|
RISB1959 |
Pyrrhocoridae
Order: Hemiptera
|
None
|
8.23% |
8.2
|
Providencia sp. PROV040
Species-level Match
|
RISB1574 |
Bactrocera tau
Order: Diptera
|
could attract male and female B. tau
|
1.88% |
7.6
|
Providencia sp. PROV040
Species-level Match
|
RISB0984 |
Nasonia vitripennis
Order: Hymenoptera
|
may highly associated with diapause
|
1.88% |
7.6
|
Klebsiella pneumoniae
Species-level Match
|
RISB2459 |
Bombyx mori
Order: Lepidoptera
|
degradation of cellulose, xylan, pectin and starch
|
1.47% |
7.5
|
Escherichia coli
Species-level Match
|
RISB2120 |
Galleria mellonella
Order: Lepidoptera
|
mediate trans-generational immune priming
|
1.42% |
7.2
|
Blattabacterium sp. (Blattella germanica)
Species-level Match
|
RISB1534 |
Periplaneta fuliginosa
Order: Blattodea
|
involved in uric acid degradation, nitrogen assimilation and nutrient provisioning
|
0.54% |
7.2
|
Blattabacterium cuenoti
Species-level Match
|
RISB0518 |
Cryptocercus punctulatus
Order: Blattodea
|
collaborative arginine biosynthesis
|
0.98% |
6.7
|
Enterococcus casseliflavus
Species-level Match
|
RISB1755 |
Spodoptera frugiperda
Order: Lepidoptera
|
may influence the metabolization of pesticides in insects
|
0.43% |
6.6
|
Enterococcus casseliflavus
Species-level Match
|
RISB1991 |
Diatraea saccharalis
Order: Lepidoptera
|
possess cellulose degrading activity
|
0.43% |
6.2
|
Salmonella enterica
Species-level Match
|
RISB0413 |
Melanaphis sacchari
Order: Hemiptera
|
None
|
1.15% |
6.2
|
Chryseobacterium sp. Y16C
Species-level Match
|
RISB2092 |
Aedes aegypti
Order: Diptera
|
axenic larvae cannot develop
|
0.36% |
5.9
|
Chryseobacterium sp. MYb264
Species-level Match
|
RISB2092 |
Aedes aegypti
Order: Diptera
|
axenic larvae cannot develop
|
0.19% |
5.8
|
Lactobacillus
|
RISB1866 |
Drosophila melanogaster
Order: Diptera
|
The bacterial cells may thus be able to ameliorate the pH of the acidic region, by the release of weak bases.Additionally, the bacteria have a complex relationship with physiological processes which may affect ionic homeostasis in the gut, such as nutrition and immune function
|
0.39% |
5.4
|
Candidatus Erwinia haradaeae
Species-level Match
|
RISB1632 |
Lachninae
Order: Hemiptera
|
None
|
0.16% |
5.2
|
Apibacter
|
RISB0603 |
Apis cerana
Order: Hymenoptera
|
The acquisition of genes for the degradation of the toxic monosaccharides potentiates Apibacter with the ability to utilize the pollen hydrolysis products, at the same time enabling monosaccharide detoxification for the host
|
0.26% |
4.7
|
Lactobacillus
|
RISB0292 |
Lymantria dispar asiatica
Order: Lepidoptera
|
Beauveria bassiana infection-based assays showed that the mortality of non-axenic L. dispar asiatica larvae was significantly higher than that of axenic larvae at 72 h.
|
0.39% |
3.8
|
Proteus
|
RISB2315 |
Aedes aegypti
Order: Diptera
|
upregulates AMP gene expression, resulting in suppression of DENV infection in the mosquito gut epithelium
|
1.21% |
3.3
|
Lactobacillus
|
RISB0715 |
Spodoptera frugiperda
Order: Lepidoptera
|
Have the function of nutrient absorption, energy metabolism, the plant’s secondary metabolites degradation, insect immunity regulation, and so on
|
0.39% |
3.3
|
Exiguobacterium
|
RISB0007 |
Phormia regina
Order: Diptera
|
prompted oviposition by flies; The flies' oviposition decisions appear to be guided by bacteria-derived semiochemicals as the bacteria
|
0.53% |
3.2
|
Streptococcus
|
RISB2625 |
Galleria mellonella
Order: Lepidoptera
|
suppress bacteria ingested with food by producing bacteriocin and by releasing a lysozyme like enzyme
|
1.02% |
3.0
|
Bacteroides
|
RISB0256 |
Leptocybe invasa
Order: Hymenoptera
|
Differences in Male-Killing Rickettsia Bacteria between Lineages of the Invasive Gall-Causing Pest Leptocybe invasa
|
0.64% |
2.9
|
Bacteroides
|
RISB0090 |
Hyphantria cunea
Order: Lepidoptera
|
enhance the compatibility of invasive pests to new hosts and enable more rapid adaptation to new habitats.
|
0.64% |
2.8
|
Streptococcus
|
RISB2624 |
Reticulitermes flavipes
Order: Blattodea
|
can be broken down into substances such as carbon dioxide, ammonia and acetic acid
|
1.02% |
2.7
|
Psychrobacter
|
RISB1773 |
Calliphoridae
Order: Diptera
|
it shows physiological adaptation to survival in warmer temperatures and has been previously associated with food spoilage
|
0.21% |
2.7
|
Sphingomonas
|
RISB0420 |
Aphis gossypii
Order: Hemiptera
|
Sphingomonas could mediate A. gossypii resistance to imidacloprid by hydroxylation and nitroreduction
|
0.45% |
2.5
|
Sphingomonas
|
RISB1307 |
Aphis gossypii
Order: Hemiptera
|
have been previously described in associations with phloem-feeding insects, in low abundances
|
0.45% |
2.3
|
Streptococcus
|
RISB2604 |
Homona magnanima
Order: Lepidoptera
|
influence the growth of Bacillus thuringiensis in the larvae
|
1.02% |
2.2
|
Proteus
|
RISB2460 |
Bombyx mori
Order: Lepidoptera
|
degradation of cellulose, xylan, pectin and starch
|
1.21% |
2.2
|
Flavobacterium
|
RISB0659 |
Melanaphis bambusae
Order: Hemiptera
|
None
|
2.15% |
2.2
|
Sphingomonas
|
RISB0134 |
Spodoptera frugiperda
Order: Lepidoptera
|
provide a protective effect to against chlorantraniliprole stress to S. frugiperda
|
0.45% |
2.1
|
Lysinibacillus
|
RISB1416 |
Psammotermes hypostoma
Order: Blattodea
|
isolates showed significant cellulolytic activity
|
1.08% |
2.1
|
Paraclostridium
|
RISB0028 |
Sesamia inferens
Order: Lepidoptera
|
degrade Chlorpyrifos and Chlorantraniliprole in vitro
|
0.37% |
1.4
|
Exiguobacterium
|
RISB0582 |
Aleurodicus rugioperculatus
Order: Hemiptera
|
may indirectly affect whitefly oviposition
|
0.53% |
1.4
|
Peribacillus
|
RISB1877 |
Aedes aegypti
Order: Diptera
|
gut microbiome
|
0.90% |
1.2
|
Priestia
|
RISB0839 |
Helicoverpa armigera
Order: Lepidoptera
|
producing amylase
|
0.64% |
1.0
|
Legionella
|
RISB1687 |
Polyplax serrata
Order: Phthiraptera
|
None
|
0.98% |
1.0
|
Helicobacter
|
RISB0662 |
Melanaphis bambusae
Order: Hemiptera
|
None
|
0.41% |
0.4
|
Myroides
|
RISB0626 |
Musca altica
Order: Diptera
|
None
|
0.29% |
0.3
|
Apibacter
|
RISB0604 |
Apis cerana
Order: Hymenoptera
|
None
|
0.26% |
0.3
|
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