ShethRU, CabralV, ChenSP, et al.Manipulating bacterial communities by in situ microbiome engineering. Trends Genet, 2016; 32:189–200. DOI: 10.1016/j.tig.2016.01.005.
2.
RubinBE, DiamondS, CressBF, et al.Species- and site-specific genome editing in complex bacterial communities. Nat Microbiol, 2022; 7:34–47. DOI: 10.1038/s41564-021-01014-7.
3.
PetersJE, MakarovaKS, ShmakovS, et al.Recruitment of CRISPR-Cas systems by Tn7-like transposons. Proc Natl Acad Sci U S A, 2017; 114:E7358–E7366. DOI: 10.1073/pnas.1709035114.
4.
FaureG, ShmakovSA, YanWX, et al.CRISPR-Cas in mobile genetic elements: counter-defence and beyond. Nat Rev Microbiol, 2019; 17:513–525. DOI: 10.1038/s41579-019-0204-7.
5.
StreckerJ, LadhaA, GardnerZ, et al.RNA-guided DNA insertion with CRISPR-associated transposases. Science, 2019; 365:48–53. DOI: 10.1126/science.aax9181.
6.
KlompeSE, VoPLH, Halpin-HealyTS, et al.Transposon-encoded CRISPR-Cas systems direct RNA-guided DNA integration. Nature, 2019; 571:219–225. DOI: 10.1038/s41586-019-1323-z.
7.
VoPLH, RondaC, KlompeSE, et al.CRISPR RNA-guided integrases for high-efficiency, multiplexed bacterial genome engineering. Nat Biotechnol, 2021; 39:480–489. DOI: 10.1038/s41587-020-00745-y.