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Shrinking in the dark: Parallel endosymbiont genome erosions are associated with repeated host transitions to an underground life.
Beasley-Hall, Perry G; Kinjo, Yukihiro; Rose, Harley A; Walker, James; Foster, Charles S P; Kovacs, Toby G L; Bourguignon, Thomas; Ho, Simon Y W; Lo, Nathan.
Afiliación
  • Beasley-Hall PG; School of Life and Environmental Sciences, University of Sydney, Sydney, New South Wales, Australia.
  • Kinjo Y; School of Biological Sciences, University of Adelaide, Adelaide, South Australia, Australia.
  • Rose HA; Evolutionary Genomics Unit, Okinawa Institute of Science & Technology Graduate University, Onna-son, Okinawa, Japan.
  • Walker J; School of Life and Environmental Sciences, University of Sydney, Sydney, New South Wales, Australia.
  • Foster CSP; Australian Government Department of Agriculture Water and Environment, Canberra, Australia.
  • Kovacs TGL; School of Biomedical Sciences, University of New South Wales, Sydney, New South Wales, Australia.
  • Bourguignon T; School of Life and Environmental Sciences, University of Sydney, Sydney, New South Wales, Australia.
  • Ho SYW; Australian Government Department of Agriculture Water and Environment, Canberra, Australia.
  • Lo N; School of Life and Environmental Sciences, University of Sydney, Sydney, New South Wales, Australia.
Insect Sci ; 2024 Mar 10.
Article en En | MEDLINE | ID: mdl-38462506
ABSTRACT
Microbial symbioses have had profound impacts on the evolution of animals. Conversely, changes in host biology may impact the evolutionary trajectory of symbionts themselves. Blattabacterium cuenoti is present in almost all cockroach species and enables hosts to subsist on a nutrient-poor diet. To investigate if host biology has impacted Blattabacterium at the genomic level, we sequenced and analyzed 25 genomes from Australian soil-burrowing cockroaches (Blaberidae Panesthiinae), which have undergone at least seven separate subterranean, subsocial transitions from above-ground, wood-feeding ancestors. We find at least three independent instances of genome erosion have occurred in Blattabacterium strains exclusive to Australian soil-burrowing cockroaches. These shrinkages have involved the repeated inactivation of genes involved in amino acid biosynthesis and nitrogen recycling, the core role of Blattabacterium in the host-symbiont relationship. The most drastic of these erosions have occurred in hosts thought to have transitioned underground the earliest relative to other lineages, further suggestive of a link between gene loss in Blattabacterium and the burrowing behavior of hosts. As Blattabacterium is unable to fulfill its core function in certain host lineages, these findings suggest soil-burrowing cockroaches must acquire these nutrients from novel sources. Our study represents one of the first cases, to our knowledge, of parallel host adaptations leading to concomitant parallelism in their mutualistic symbionts, further underscoring the intimate relationship between these two partners.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Insect Sci Año: 2024 Tipo del documento: Article País de afiliación: Australia

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Insect Sci Año: 2024 Tipo del documento: Article País de afiliación: Australia