Abstract
Abstract
The molecular epidemiology of
Acinetobacter
, which is almost exclusively culture-dependent, has centered mainly on clinical isolates of
A. baumannii
. Yet, this overlooks sources not amenable to microbial culture and many non-
A. baumannii
species. Here, by analysing metagenomic projects from public transport systems worldwide, we show that metagenome-assembled genomes (MAGs) are highly relevant for assessing the unrecognized diversity of
Acinetobacter
. We recovered 839
Acinetobacter
MAGs, with 269 being high-quality MAGs. The high-quality MAGs were across more than 20 well-defined
Acinetobacter
species; however, five species (
A. nosocomilalis, A. ursingii, A. radioresistens, A. schindleri
, and
A. variabilis
) had the most MAGs. Pangenome and phylogenetic diversity analyses of 685 genomes plus the 269 high-quality MAGs from those 5 species showed that MAGs are an important source of both lineage and gene diversity. Also, F
ST
analyses and genome phylogenies show that for some species there is no genetic differentiation between MAGs and clinical isolates, implying transmission between hospitals and public transport settings. In addition to finding the antibiotic resistance genes (ARGs) in MAGs, we implemented an
ad hoc
strategy (leveraging the use of genomes) to recover considerably more ARGs. PCoA and PERMANOVA analyses show that, whereas in
A. nosocomialis
and
A. ursingii
, the ARG profiles of MAGs and clinical genomes are different, in
A. radioresistens
and
A. schindleri
, the ARG profiles are not different. Finally, some clinically important ARGs, such as
sul1
and
sul2, aadA
, and
blaOXA
23
, were found in all or some of the 5 species. Our study shows how combining MAGs and regular genomes is a powerful strategy for better appraising the genomic diversity (including the resistome) of
Acinetobacter
. On a broader level, our study showcases the importance of MAGs for genomic surveillance of man-made environments with clear public health implications.