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Table 2 Immune-related ESTs and comparison of gene expression between naive larvae, mock-infected larvae and larvae challenged with Escherichia coli.

From: Identification of the Weevil immune genes and their expression in the bacteriome tissue

EST

Protein description

E-value

Target Organism

UniProt Acc. Num.

qRT-PCR Fold change

 

Antibacterial peptides

   

sterile injury

septic injury

INF-18

Coleoptericin

3E-15

Zophobas atratus

P80032

11.4*

86.1* (*)

INF-42

Diptericin A

2.6

Glossina morsitans

Q8WTD5

> 10*

> 300* (*)

INF-145

Acaloleptin A

2E-15

Acalolepta luxuriosa

Q76K70

1.8

43.1*

INF-163

Cecropin A1

0.68

Drosophila mauritiana

P81685

1

31.5*

INF-165

Sarcotoxin II-1

0.67

Sarcophaga peregrina

P24491

0.8

31.6*

INF-217

Tenecin-1

3E-13

Tenebrio molitor

Q27023

9.7*

314.9* (*)

INF-479

Luxuriosin

0.18

Acalolepta luxuriosa

Q60FC9

2.8*

4.5*

 

Lysozymes

     

INF-152

Lysozyme i-1

1E-05

Anopheles gambiae

Q6GU90

7.8*

5.2*

INF-282

Lysozyme C-1

6E-17

Anas platyrhynchos

P00705

7.1*

5.4*

 

PGRP

     

INF-9

PGRP sb2

7E-57

Aedes aegypti

Q1HRH3

2.3*

6.7* (*)

INF-441

PGRP

9E-38

Biomphalaria glabrata

A0T2Q1

7.8*

11.6*

 

Immune regulator

     

INF-359

TOLLIP

3E-48

Mus musculus

Q9QZ06

1.2

1.7

 

Phenoloxidase pathway

     

INF-506

PPAF

2E-15

Holotrichia diomphalia

Q9GRW0

2.8*

2.7*

INF-74

Serpin-4A

2E-20

Manduca sexta

Q6Q2D8

2.8*

2.9*

 

Proteases a

     

INF-20

IMPI

2E-11

Galleria mellonella

P82176

2.3*

3.4*

INF-91

Cysteine-rich venom-like protein

7E-09

Aedes albopictus

Q5MIW2

3.4*

7.5* (*)

INF-258

Pattern recognition serine proteinase

7E-28

Manduca sexta

Q69BL0

ND

ND

INF-459

Hemolymph proteinase 17

3E-10

Manduca sexta

Q5MPB8

1.7

4.4

INF-515

Trypsin-like serine proteinase

5E-27

Anthonomus grandis

Q64ID5

1.4

1.1

 

Cytoskeleton

     

INF-13

profilin

3E-29

Apis mellifera

Q6QEJ7

0.9

0.8

-

actin

-

Sitophilus zeamais

-

1

1.3

  1. ESTs were analyzed as described in Materials and Methods and classified according to gene family or function. Transcripts were quantitated by qRT-PCR in untreated aposymbiotic larvae (control), in larvae six hours after a mock-infection (sterile injury) or an E. coli infection (septic injury). The fold-change of gene expression after sterile or septic injury is expressed relative to the transcript levels in untreated larvae. For each sample, the transcript level is estimated from the mean of three independent measurements after normalization with the expression of the gapdh gene. The transcript amounts of the genes corresponding to the EST INF-42 and INF-258 are too weak to be quantified in the control larvae and in all the samples, respectively. Comparisons of transcript levels between the three samples were made using nonparametric tests. A significant increase in transcript level after sterile or septic injury is indicated by an asterisk (p < 0.05). A significant difference between sterile and septic injury is indicated by a second asterisk (p < 0.05). Acc. Num., accession number; ND, non-determined. a. Proteases can represent either signaling proteins or immune effectors.