Matches in SemOpenAlex for { <https://semopenalex.org/work/W2624224895> ?p ?o ?g. }
- W2624224895 abstract "Obligate bacterial primary (P-) endosymbionts that are maternally inherited and codiverge with hosts are widespread across insect lineages with nutritionally restricted diets. Secondary (S-) endosymbionts are mostly facultative, but in some hosts, they complement P-endosymbiont function and therefore become obligate. Phylogenetic evidence exists for host switching and replacement of S-endosymbionts. The community dynamics that precede endosymbiont replacement and complementation have been little studied across host species, yet they are fundamental to the evolution of endosymbiosis.We performed bacterial 16S rRNA gene amplicon sequencing of 25 psyllid species (Hemiptera, Psylloidea) across different developmental stages and ecological niches by focusing on the characterisation of the bacteria other than the universally present P-endosymbiont Carsonella (Gammaproteobacteria). Most species harboured only one dominant representative of diverse gammaproteobacterial S-endosymbionts that was consistently detected across all host individuals and populations (Arsenophonus in eight species, Sodalis or Sodalis-like bacteria in four species, unclassified Enterobacteriaceae in eight species). The identity of this dominant obligate S-endosymbiont varied across closely related host species. Unexpectedly, five psyllid species had two or three co-occurring endosymbiont species other than Carsonella within all host individuals, including a Rickettsiella-like bacterium (Gammaproteobacteria) in one psyllid species. Based on standard and quantitative PCR, all psyllids carried Carsonella, at higher titres than their dominant S-endosymbionts. Some psyllids also had Alphaproteobacteria (Lariskella, Rickettsia, Wolbachia) at varying prevalence. Incidence of other bacteria, including known plant pathogens, was low. Ecological niche of gall-forming, lerp-forming and free-living psyllid species did not impact endosymbiont communities. Two flush-feeding psyllid species had population-specific differences, and this was attributable to the higher endosymbiont diversity in native ranges and the absence of some endosymbionts in invasive ranges.Our data support the hypothesis of strict vertical transmission of minimal core communities of bacteria in psyllids. We also found evidence for S-endosymbiont replacement across closely related psyllid species. Multiple dominant S-endosymbionts present in some host species, including at low titre, constitute potential examples of incipient endosymbiont complementation or replacement. Our multiple comparisons of deep-sequenced minimal insect bacterial communities exposed the dynamics involved in shaping insect endosymbiosis." @default.
- W2624224895 created "2017-06-15" @default.
- W2624224895 creator A5011253402 @default.
- W2624224895 creator A5055871051 @default.
- W2624224895 creator A5064691239 @default.
- W2624224895 date "2017-06-06" @default.
- W2624224895 modified "2023-10-17" @default.
- W2624224895 title "Symbionts in waiting: the dynamics of incipient endosymbiont complementation and replacement in minimal bacterial communities of psyllids" @default.
- W2624224895 cites W1494139448 @default.
- W2624224895 cites W1549071235 @default.
- W2624224895 cites W1553315593 @default.
- W2624224895 cites W1883182473 @default.
- W2624224895 cites W1893751639 @default.
- W2624224895 cites W1933408364 @default.
- W2624224895 cites W1939121325 @default.
- W2624224895 cites W1943810016 @default.
- W2624224895 cites W1968179480 @default.
- W2624224895 cites W1968523619 @default.
- W2624224895 cites W1972136915 @default.
- W2624224895 cites W1973253956 @default.
- W2624224895 cites W1979655623 @default.
- W2624224895 cites W1980383915 @default.
- W2624224895 cites W1980961885 @default.
- W2624224895 cites W1993716424 @default.
- W2624224895 cites W1994871845 @default.
- W2624224895 cites W1998255846 @default.
- W2624224895 cites W2001736765 @default.
- W2624224895 cites W2013499390 @default.
- W2624224895 cites W2013749849 @default.
- W2624224895 cites W2014438907 @default.
- W2624224895 cites W2017412116 @default.
- W2624224895 cites W2026900812 @default.
- W2624224895 cites W2027926011 @default.
- W2624224895 cites W2035576673 @default.
- W2624224895 cites W2036313192 @default.
- W2624224895 cites W2047526274 @default.
- W2624224895 cites W2048883964 @default.
- W2624224895 cites W2055043387 @default.
- W2624224895 cites W2060834037 @default.
- W2624224895 cites W2064306419 @default.
- W2624224895 cites W2064683609 @default.
- W2624224895 cites W2071986366 @default.
- W2624224895 cites W2072970694 @default.
- W2624224895 cites W2073336015 @default.
- W2624224895 cites W2079692801 @default.
- W2624224895 cites W2080229897 @default.
- W2624224895 cites W2092088519 @default.
- W2624224895 cites W2093172628 @default.
- W2624224895 cites W2096285045 @default.
- W2624224895 cites W2099490952 @default.
- W2624224895 cites W2102131597 @default.
- W2624224895 cites W2104936527 @default.
- W2624224895 cites W2105368763 @default.
- W2624224895 cites W2105560084 @default.
- W2624224895 cites W2106082795 @default.
- W2624224895 cites W2110738428 @default.
- W2624224895 cites W2112509067 @default.
- W2624224895 cites W2114570899 @default.
- W2624224895 cites W2115371650 @default.
- W2624224895 cites W2120973578 @default.
- W2624224895 cites W2122209826 @default.
- W2624224895 cites W2123331734 @default.
- W2624224895 cites W2124351063 @default.
- W2624224895 cites W2125116467 @default.
- W2624224895 cites W2125554684 @default.
- W2624224895 cites W2128023798 @default.
- W2624224895 cites W2129188176 @default.
- W2624224895 cites W2132181441 @default.
- W2624224895 cites W2141718064 @default.
- W2624224895 cites W2145465491 @default.
- W2624224895 cites W2148698435 @default.
- W2624224895 cites W2150570211 @default.
- W2624224895 cites W2151534052 @default.
- W2624224895 cites W2152207030 @default.
- W2624224895 cites W2154486014 @default.
- W2624224895 cites W2155776392 @default.
- W2624224895 cites W2158411546 @default.
- W2624224895 cites W2159267296 @default.
- W2624224895 cites W2160370679 @default.
- W2624224895 cites W2160570214 @default.
- W2624224895 cites W2162912374 @default.
- W2624224895 cites W2168917114 @default.
- W2624224895 cites W2170438129 @default.
- W2624224895 cites W2172820226 @default.
- W2624224895 cites W2175861924 @default.
- W2624224895 cites W2176648664 @default.
- W2624224895 cites W2342667878 @default.
- W2624224895 cites W2346018873 @default.
- W2624224895 cites W2516559547 @default.
- W2624224895 cites W2529001606 @default.
- W2624224895 cites W2604607190 @default.
- W2624224895 cites W2604963620 @default.
- W2624224895 cites W2622596994 @default.
- W2624224895 cites W2077384602 @default.
- W2624224895 doi "https://doi.org/10.1186/s40168-017-0276-4" @default.
- W2624224895 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5461708" @default.
- W2624224895 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/28587661" @default.
- W2624224895 hasPublicationYear "2017" @default.
- W2624224895 type Work @default.
- W2624224895 sameAs 2624224895 @default.