FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W4282960328> ?p ?o ?g. }

• W4282960328 endingPage "e13574" @default.
• W4282960328 startingPage "e13574" @default.
• W4282960328 abstract "Effective coral restoration must include comprehensive investigations of the targeted coral community that consider all aspects of the coral holobiont—the coral host, symbiotic algae, and microbiome. For example, the richness and composition of microorganisms associated with corals may be indicative of the corals’ health status and thus help guide restoration activities. Potential differences in microbiomes of restoration corals due to differences in host genetics, environmental condition, or geographic location, may then influence outplant success. The objective of the present study was to characterize and compare the microbiomes of apparently healthy Acropora cervicornis genotypes that were originally collected from environmentally distinct regions of Florida’s Coral Reef and sampled after residing within Mote Marine Laboratory’s in situ nursery near Looe Key, FL (USA) for multiple years. By using 16S rRNA high-throughput sequencing, we described the microbial communities of 74 A. cervicornis genotypes originating from the Lower Florida Keys ( n = 40 genotypes), the Middle Florida Keys ( n = 15 genotypes), and the Upper Florida Keys ( n = 19 genotypes). Our findings demonstrated that the bacterial communities of A. cervicornis originating from the Lower Keys were significantly different from the bacterial communities of those originating from the Upper and Middle Keys even after these corals were held within the same common garden nursery for an average of 3.4 years. However, the bacterial communities of corals originating in the Upper Keys were not significantly different from those in the Middle Keys. The majority of the genotypes, regardless of collection region, were dominated by Alphaproteobacteria, namely an obligate intracellular parasite of the genus Ca. Aquarickettsia . Genotypes from the Upper and Middle Keys also had high relative abundances of Spirochaeta bacteria. Several genotypes originating from both the Lower and Upper Keys had lower abundances of Aquarickettsia , resulting in significantly higher species richness and diversity. Low abundance of Aquarickettsia has been previously identified as a signature of disease resistance. While the low- Aquarickettsia corals from both the Upper and Lower Keys had high abundances of an unclassified Proteobacteria, the genotypes in the Upper Keys were also dominated by Spirochaeta . The results of this study suggest that the abundance of Aquarickettsia and Spirochaeta may play an important role in distinguishing bacterial communities among A. cervicornis populations and compositional differences of these bacterial communities may be driven by regional processes that are influenced by both the environmental history and genetic relatedness of the host. Additionally, the high microbial diversity of low- Aquarickettsia genotypes may provide resilience to their hosts, and these genotypes may be a potential resource for restoration practices and management." @default.
• W4282960328 created "2022-06-17" @default.
• W4282960328 creator A5014373122 @default.
• W4282960328 creator A5015893228 @default.
• W4282960328 creator A5018624644 @default.
• W4282960328 creator A5024060356 @default.
• W4282960328 creator A5029699751 @default.
• W4282960328 creator A5051444974 @default.
• W4282960328 creator A5072096609 @default.
• W4282960328 date "2022-06-16" @default.
• W4282960328 modified "2023-10-14" @default.
• W4282960328 title "Geographically driven differences in microbiomes of <i>Acropora cervicornis</i> originating from different regions of Florida’s Coral Reef" @default.
• W4282960328 cites W1941978790 @default.
• W4282960328 cites W1964504982 @default.
• W4282960328 cites W1978411092 @default.
• W4282960328 cites W1980453934 @default.
• W4282960328 cites W1984682151 @default.
• W4282960328 cites W2019595204 @default.
• W4282960328 cites W2024763652 @default.
• W4282960328 cites W2031423287 @default.
• W4282960328 cites W2032901019 @default.
• W4282960328 cites W2034285706 @default.
• W4282960328 cites W2040127188 @default.
• W4282960328 cites W2050319707 @default.
• W4282960328 cites W2055203500 @default.
• W4282960328 cites W2056279562 @default.
• W4282960328 cites W2057524613 @default.
• W4282960328 cites W2061325711 @default.
• W4282960328 cites W2069200950 @default.
• W4282960328 cites W2071918757 @default.
• W4282960328 cites W2080283023 @default.
• W4282960328 cites W2085372140 @default.
• W4282960328 cites W2093956729 @default.
• W4282960328 cites W2098751975 @default.
• W4282960328 cites W2099543625 @default.
• W4282960328 cites W2115568441 @default.
• W4282960328 cites W2118040479 @default.
• W4282960328 cites W2121030746 @default.
• W4282960328 cites W2122890606 @default.
• W4282960328 cites W2135768936 @default.
• W4282960328 cites W2136811216 @default.
• W4282960328 cites W2148989977 @default.
• W4282960328 cites W2170025869 @default.
• W4282960328 cites W2222863536 @default.
• W4282960328 cites W2294512339 @default.
• W4282960328 cites W2310182301 @default.
• W4282960328 cites W2341876054 @default.
• W4282960328 cites W2400789937 @default.
• W4282960328 cites W2401404581 @default.
• W4282960328 cites W2414643416 @default.
• W4282960328 cites W2473393292 @default.
• W4282960328 cites W2474266558 @default.
• W4282960328 cites W2531135086 @default.
• W4282960328 cites W2549976854 @default.
• W4282960328 cites W2562261106 @default.
• W4282960328 cites W2568232135 @default.
• W4282960328 cites W2592058522 @default.
• W4282960328 cites W2594645998 @default.
• W4282960328 cites W2598323208 @default.
• W4282960328 cites W2609673519 @default.
• W4282960328 cites W2626737126 @default.
• W4282960328 cites W2732008330 @default.
• W4282960328 cites W2733219937 @default.
• W4282960328 cites W2745325622 @default.
• W4282960328 cites W2749811363 @default.
• W4282960328 cites W2751569690 @default.
• W4282960328 cites W2790924554 @default.
• W4282960328 cites W2794552359 @default.
• W4282960328 cites W2891469253 @default.
• W4282960328 cites W2901282808 @default.
• W4282960328 cites W2942905806 @default.
• W4282960328 cites W2943051585 @default.
• W4282960328 cites W2951317665 @default.
• W4282960328 cites W2961556035 @default.
• W4282960328 cites W2963826875 @default.
• W4282960328 cites W2965387242 @default.
• W4282960328 cites W2985333081 @default.
• W4282960328 cites W2992679780 @default.
• W4282960328 cites W2994012659 @default.
• W4282960328 cites W3003324864 @default.
• W4282960328 cites W3017015330 @default.
• W4282960328 cites W3021043347 @default.
• W4282960328 cites W3029875029 @default.
• W4282960328 cites W3036054867 @default.
• W4282960328 cites W3043922114 @default.
• W4282960328 cites W3081423058 @default.
• W4282960328 cites W3089035665 @default.
• W4282960328 cites W3092228463 @default.
• W4282960328 cites W3134388464 @default.
• W4282960328 cites W3173668217 @default.
• W4282960328 cites W3192186341 @default.
• W4282960328 cites W3201319368 @default.
• W4282960328 cites W4206818946 @default.
• W4282960328 cites W4211013950 @default.
• W4282960328 cites W4226498736 @default.
• W4282960328 doi "https://doi.org/10.7717/peerj.13574" @default.
• W4282960328 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/35729906" @default.
• W4282960328 hasPublicationYear "2022" @default.

• next