From: Overview of paratransgenesis as a strategy to control pathogen transmission by insect vectors
Insect vectors | Transformed microbes used + effector genes | Paratransgenesis innovation | References |
---|---|---|---|
Rhodnius prolixus | Rhodococcus rhodnii + thiostrepton resistance | Original technique described | [66] |
R. prolixus | R. rhodnii + cecropin A | Killing of Trypanosoma cruzi | |
R. prolixus/Triatoma infestans | R. rhodnii/Corynebacterium sp. + AMPs, rDB3 and endoglucanase | Combinations of effector molecules kill T. cruzi | |
Anopheles gambiae | Metarhizium anisopliae + scorpine and scorpine fusion protein | Combinations of effector molecules kill Plasmodium | [100] |
Anopheles stephensi | Serratia ASI + 5 anti-Plasmodium effector proteins | Combinations of effector molecules kill Plasmodium | [120] |
Anopheles gambiae | Microbiome endosymbionts fully identified for the first time | High-throughput sequencing introduced | [132] |
R. prolixus | R. rhodnii + rDB3 antibody fragment | Semi-field simulation of transgenic bacteria spread in CRUZIGARD | [73] |
Homalodisca vitripennisa | Pantoea agglomeransgfp | Semi-field simulation of transgenic bacteria spread in hydrogel | [128] |
An. stephensi/An. gambiae | Asaiagfp | Semi-field simulation of transgenic bacteria spread | [53] |
An. stephensi | Serratia AS1-mCherry and AS1-gfp | Semi-field simulation of transgenic bacteria spread | [120] |
R. prolixus | R. rhodnii and Gordona rubropertinctus | Model showing negligible risk of horizontal transfer of transgenic bacteria | [133] |
An. stephensi | Serratia ASI-gfp + mCheery and kanR genes/+ microbiome in vivo | No horizontal transfer of transgenic bacteria genetic material in vivo | |
Anopheles spp. | P. agglomerans | Modelling paratransgensisib | [130] |
An. stephensi | Serratia ASI-gfp + mCheery and kanR genes/+ microbiome in vivo | Transiently expressed plasmids for checking environmental safety of released genes | [134] |
An. stephensi | Asaia + scorpine | Transgene only expressed after blood meal, thus reducing fitness costs | [126] |
R. prolixus | R. rhodnii and Escherichia coli expressing dsRNA | RNAi and knockdown of vector genesc | |
Anopheles spp. | Asaia RNaseIII mutant created | Potential for developing an efficient RNAi-based paratransgenesis for vector or parasite gene knockdown | |
An. gambiae | CRISPR/Cas9 is a new method of microbe transformation | Potential to transform microbes for paratransgenesis and also mediate gene silencing | |
Aedes albopictus | MDVs | miRNA expression system with recombinant MDVs stable for silencing mosquito genes | [90] |