TY - JOUR
T1 - Chromosomal integrons are genetically and functionally isolated units of genomes
AU - Blanco, Paula
AU - da Roza, Filipa Trigo
AU - Toribio-Celestino, Laura
AU - García-Pastor, Lucía
AU - Caselli, Niccolò
AU - Morón, Álvaro
AU - Ojeda, Francisco
AU - Darracq, Baptiste
AU - Vergara, Ester
AU - Amaro, Francisco
AU - Millán, Álvaro San
AU - Skovgaard, Ole
AU - Mazel, Didier
AU - Loot, Céline
AU - Escudero, José Antonio
PY - 2024/11/11
Y1 - 2024/11/11
N2 - Integrons are genetic elements that increase the evolvability of bacteria by capturing new genes and stockpiling them in arrays. Sedentary chromosomal integrons (SCIs) can be massive and highly stabilized structures encoding hundreds of genes, whose function remains generally unknown. SCIs have co-evolved with the host for aeons and are highly intertwined with their physiology from a mechanistic point of view. But, paradoxically, other aspects, like their variable content and location within the genome, suggest a high genetic and functional independence. In this work, we have explored the connection of SCIs to their host genome using as a model the Superintegron (SI), a 179-cassette long SCI in the genome of Vibrio cholerae N16961. We have relocated and deleted the SI using SeqDelTA, a novel method that allows to counteract the strong stabilization conferred by toxin–antitoxin systems within the array. We have characterized in depth the impact in V. cholerae’s physiology, measuring fitness, chromosome replication dynamics, persistence, transcriptomics, phenomics, natural competence, virulence and resistance against protist grazing. The deletion of the SI did not produce detectable effects in any condition, proving that—despite millions of years of co-evolution—SCIs are genetically and functionally isolated units of genomes.
AB - Integrons are genetic elements that increase the evolvability of bacteria by capturing new genes and stockpiling them in arrays. Sedentary chromosomal integrons (SCIs) can be massive and highly stabilized structures encoding hundreds of genes, whose function remains generally unknown. SCIs have co-evolved with the host for aeons and are highly intertwined with their physiology from a mechanistic point of view. But, paradoxically, other aspects, like their variable content and location within the genome, suggest a high genetic and functional independence. In this work, we have explored the connection of SCIs to their host genome using as a model the Superintegron (SI), a 179-cassette long SCI in the genome of Vibrio cholerae N16961. We have relocated and deleted the SI using SeqDelTA, a novel method that allows to counteract the strong stabilization conferred by toxin–antitoxin systems within the array. We have characterized in depth the impact in V. cholerae’s physiology, measuring fitness, chromosome replication dynamics, persistence, transcriptomics, phenomics, natural competence, virulence and resistance against protist grazing. The deletion of the SI did not produce detectable effects in any condition, proving that—despite millions of years of co-evolution—SCIs are genetically and functionally isolated units of genomes.
U2 - 10.1093/nar/gkae866
DO - 10.1093/nar/gkae866
M3 - Journal article
C2 - 39385642
AN - SCOPUS:85208772753
SN - 0305-1048
VL - 52
SP - 12565
EP - 12581
JO - Nucleic Acids Research
JF - Nucleic Acids Research
IS - 20
ER -