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. 2018 Nov 29;8:17456. doi: 10.1038/s41598-018-35658-z

Table 2.

Wolbachia and Asaia infection prevalence rates in adult female mosquitoes using three conserved Wolbachia genes (16S rRNA, ftsZ and wsp).

Mosquito species Number Wolbachia gene PCR amplification Prevalence (%) Fisher’s exact post hoc P value (Wolbachia vs. Asaia)
16S rRNA ftsZ wsp Wolbachia Asaia
Aedes albocephalus 1 0 0 0
Aedes circumlateolus 1 0 0 0 100
(20–100)
Aedomyia furfuria 2 0 0 0 100
(34–100)
Aedomyia madagascarica^ 9 9 9 9 100
(70–100)
89
(56–98)
>0.99
Culex antennatus^ 32 1 1 0 3
(1–16)
56
(38–74)
>0.99
Culex bitaeniorhynchus 12 0 0 0 58
(32–81)
Culex decens^ 17 3 3 3 18
(4–43)
18
(4–43)
0.46
Culex duttoni^ 1 1 1 0 100
(21–100)
100
(21–100)
>0.99
Culex tritaeniorhynchus^ 19 0 0 0 95
(74–100)
Culex giganteus 5 0 0 0 80
(37–96)
Culex pipiens complex 44 0 0 0 7
(1–30)
Culex poicilipes 21 0 0 0 48
(28–68)
Ficalbia circumtestacea 3 1 1 0 33
(6–79)
Mansonia uniformis^ 24 7 7 0 29
(15–49)
67
(47–82)
0.65
Uranotaenia spp^ 27 7 7 7 26
(13–45)
19
(8–37)
0.54

An individual was considered Wolbachia-infected when any one of the three Wolbachia gene fragments were amplified. Species containing resident Wolbachia strains are in bold. Wolbachia and Asaia prevalence rates are shown with 95% confidence intervals in parentheses. Fisher’s exact post hoc test P value is shown comparing Wolbachia and Asaia infections in individual mosquitoes from species that contained at least one individual of both bacterial endosymbionts. ^ denotes where CO1 sequences were obtained for phylogenetic analysis of mosquito species.