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Table 1 Molecular assays used in the study: primers and PCR conditions

From: Population dynamics, pathogen detection and insecticide resistance of mosquito and sand fly in refugee camps, Greece

 

Species

Assay

Primers (5′ → 3′)

PCR condition

Reference

Insecticide resistance assays

Culex pipiens

VGSC (1014F)/kdr - allele specific PCR

Cgd1: GTGGAACTTCACCGACTTC

Cgd2: GCAAGGCTAAGAAAAGGTTAAG

Cgd3: CCACCGTAGTGATAGGAAATTTA

Cgd4: CCACCGTAGTGATAGGAAATTTT

95 °C 5 min, 40 cycles × (94 °C 30 s, 48 °C 30 s, 72 °C 1 min), 72 °C 10 min

[26]

Cx. pipiens

CHS (1043 L) - allele specific PCR

External_F: GCAGTCCTTCGGCGATCTT

External_R: GAACAGTCCGGCGATGGATA

ATC_ R: AACAGCAAGTACATAGACGGGAT

CTC_ F: GGCTTGATCTACCTGCTGTCTC

95 °C 5 min, 28 cycles × (95 °C 30 s, 68 °C 30 s, 72 °C 1 min), 72 °C 5 min

[17]

Cx. pipiens

CHS (1043 M) - PCR and RFLP

Diagnostic I1043M_R: CCCAGGAGACGACGTTCAG

Diagnostic I1043M_F: GCCTGTCTCCATCCGCAAG

95 °C 5 min, 30 cycles × (95 °C 30 s, 60 °C 30 s, 72 °C 30 s),72 °C 5 min

[17]

Aedes albopictus

VGSC (1016G)/kdr - PCR and sequencing

F1016: TTCACCGACTTCATGCACTC

R1016: CGCAATCTGGCTTGTTAACTT

95° 3 min, 40 cycles × (94 °C 30 s, 55 °C 30 s, 72 °C 1 min), 72 °C 5 min

–

Ae. albopictus

VGSC (1532 T,1534C)/kdr - PCR and sequencing

For: GAGAACTCGCCGATGAACTT

Rev.: GACGACGAAATCGAACAGGT

Rev. for sequencing: AGCTTTCAGCGGCTTCTTC

95 °C 3 min, 40 cycles × (94 °C 30 s, 57 °C 30 s, 72 °C 1 min), 72 °C 5 min

–

Ae. albopictus

CHS (1043 L/M) - PCR and sequencing

kkv F3: TCGGAAGTCCTTCGGCTTAT TC

kkv R3: TGGATACTTCAATGGAACCTTCC

95 °C 5 min, 40 cycles × (94 °C 30 s, 55 °C 30 s, 72 °C 1 min), 72 °C 10 min

–

Anopheles (An. sacharovi, An. hyrcanus, An. maculipennis, An. claviger)

VGSC (1014F/C/S) / kdr - PCR and sequencing

KDRF: GGMGAATGGATYGAATCMATGTGGGA

KDR R2: GATGAACCRAAATTKGACAAAAGCAA

94 °C 5 min, 35 cycles × (94 °C 1 min, 50 °C 2 min, 72 °C 2 min), 72 °C 2 min

–

Sand flies (Phlebotomus perfiliewi, P. tobbi, P. simici, P. neglectus)

VGSC (1011, 1014, 1016, and 1020) / PCR and sequencing

Vssc8F: AATGTGGGATTGCATGCTGG

Vssc1bR: CGTATCATTGTCTGCAGTTGGT

95 °C 5 min, 36 cycles × (94 °C 45 s, 51 °C 50 s, 72 °C 50 s),72 °C 7 min

[27]

Species id assays

Cx. pipiens complex

AChE2- PCR diagnostic assay

ACEquin: CCTTCTTGAATGGCTGTGGCA

ACEpall: ATGGTGGAGACGCATGACG

ACEpip: GGAAACAACGACGTATGTACT

ACEtorr: TGCCTGTGCTACCAGTGATGTT

B1246s: TGGAGCCTCCTCTTCACGG

94 °C 5 min, 35 cycles × (94 °C 30 s, 55 °C 30 s, 72 °C 1 min), 72 °C 5 min

[25]

Cx. pipiens biotype

CQ11 - allele specific PCR

pipRev: CATGTTGAGCTTCGGTGAA

molRev: CCCTCCAGTAAGGTATCAAC

biotype-forward: GATCCTAGCAAGCGAGAAC

95 °C 5 min, 40 cycles × (94 °C 30 s, 54 °C 30 s, 72 °C 40 s), 72 °C 5 min

[28]

Anopheles

ITS2 - PCR and sequencing

5.8 s primer: TGTGAACTGCAGGACACATG

28 s primer: ATGCTTAAATTTAGGGGGTA

94 °C 2 min, 40 cycles × (94 °C 30 s, 53 °C 30 s, 72 °C 50 s), 72 °C 10 min

[29]

Anopheles

COI - PCR and sequencing

Cl -N-2191: CCCGGTAAAATTAAAATATAAACTTC

Cl-J-1718: GCAGGATTTGGAAATTGATTAGTTCC

94 °C 2 min, 40 cycles × (94 °C 30 s, 50 °C 30 s, 72 °C 50 s), 72 °C 10 min

[29]

Ae. albopictus

ITS2 - PCR and sequencing

5.8 s primer: TGTGAACTGCAGGACACATG

28 s primer: ATGCTTAAATTTAGGGGGTA

94 °C 10 min, 40 cycles × (94 °C 1 min, 50 °C 1 min, 72 °C 1 min), 72 °C 10 min

[30]

Sand flies

Direct multiplex PCR

Forward: TGCGGTTAAAACGTTCGTAG

perf: TAAACCCACAAATCAGAAT

sim: CTTTCATTAAATTTAGCCTGCC

papat: TAACATAAGGGGCGTATTAATATGCTTT

tob: GCGTRTTAACAATAGAGTCCATTAAA

95 °C 5 min, 32 cycles × (94 °C 40 s, 54 °C 30 s, 72 °C 1 min), 72 °C 10 min

[24]

Pathogen detection assays

Plasmodium (P. vivax, P. falciparum)

PCR 1 (Nested PCR)

rPLU5: CCTGTTGTTGCCTTAAACTTC

rPLU6: TTAAAATTGTTGCAGTTAAAACG

95 °C 5 min, 24 cycles × (94 °C 1 min, 57 °C 2 min,72 °C 2 min), 72 °C 5 min

[31]

PCR 2 (Nested PCR)

VIV-1: CGCTTCTAGCTTAATCCACATAACTGATAC

VIV-2: ACTTCCAAGCCGAAGCAAAGAAAGTCCTTA

FAL-1: TTAAACTGGTTTGGAAAACCAAATATATT

FAL-2: ACACAATGAACTCAATCATGACTACCCGTC

95 °C 5 min, 30 cycles × (94 °C 1 min, 57 °C 2 min, 72 °C 2 min), 72 °C 5 min

[31]

Flavivirus detection

Conventional one-step reverse transcriptase-PCR (RT-PCR)

Forward: TACAACATGATGGGAAAGAGAGAGAA

Reverse: GTGTCCCAGCCGGCGGTGTCATCAGC

50 °C 30 min, 95 °C 3 min, 40 cycles × (95 °C 15 s, 55 °C 20 s, 72 °C 60 s), 72 °C 10 min

[32]

West Nile virus detection

Multiplex Real Time one step RT-PCR TaqMan assay

Forward: GTGATCCATGTAAGCCCTCAGAA

Reverse: GTCTGACATTGGGCTTTGAAGTTA

FAM probe (MGB): AGGACCCCACATGTT

HEX probe (MGB): AGGACCCCACGTGCT

50 °C 15 min, 95 °C 3 min, 45 cycles × (95 °C 3 s and 60 °C 30 s)

[33, 34]

  1. VGSC Voltage gated sodium channel; CHS Chitin synthase; kdr Knock down resistance; AChE2 Acetylcholinesterase-2; CQ11 Microsatellite locus; ITS2 Internal transcribed spacer two; COI Cytochrome oxidase subunit 1; [REF] References