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1.
Mol Ecol ; 26(9): 2498-2513, 2017 May.
Article in English | MEDLINE | ID: mdl-28042895

ABSTRACT

In tropical forests, rarer species show increased sensitivity to species-specific soil pathogens and more negative effects of conspecific density on seedling survival (NDD). These patterns suggest a connection between ecology and immunity, perhaps because small population size disproportionately reduces genetic diversity of hyperdiverse loci such as immunity genes. In an experiment examining seedling roots from six species in one tropical tree community, we found that smaller populations have reduced amino acid diversity in pathogen resistance (R) genes but not the transcriptome in general. Normalized R gene amino acid diversity varied with local abundance and prior measures of differences in sensitivity to conspecific soil and NDD. After exposure to live soil, species with lower R gene diversity had reduced defence gene induction, more cosusceptibility of maternal cohorts to colonization by potentially pathogenic fungi, reduced root growth arrest (an R gene-mediated response) and their root-associated fungi showed lower induction of self-defence (antioxidants). Local abundance was not related to the ability to induce immune responses when pathogen recognition was bypassed by application of salicylic acid, a phytohormone that activates defence responses downstream of R gene signalling. These initial results support the hypothesis that smaller local tree populations have reduced R gene diversity and recognition-dependent immune responses, along with greater cosusceptibility to species-specific pathogens that may facilitate disease transmission and NDD. Locally rare species may be less able to increase their equilibrium abundance without genetic boosts to defence via immigration of novel R gene alleles from a larger and more diverse regional population.


Subject(s)
Disease Resistance/genetics , Genes, Plant , Plant Immunity/genetics , Trees/genetics , Tropical Climate , Alleles , Ecology , Forests , Genetic Variation , Population Density , Seedlings , Trees/microbiology
2.
J Appl Microbiol ; 102(6): 1612-24, 2007 Jun.
Article in English | MEDLINE | ID: mdl-17578427

ABSTRACT

AIMS: This paper investigates the diversity of polycyclic aromatic hydrocarbon (PAH)-degrading mycobacterium isolates from three different sites within United States: Montana, Texas and Indiana. METHODS AND RESULTS: All five mycobacterium isolates differed in chromosomal restriction enzyme-fragmentation patterns; three isolates possessed linear plasmids. The DNA sequence between the murA and rRNA genes were divergent but the sequence upstream of nidBA genes, encoding a dioxygenase involved in pyrene oxidation, was more highly conserved. Long-chain fatty acid analysis showed most similarity between three isolates from the same Montana site. All isolates were sensitive to rifampicin and isoniazid, used in tuberculosis treatment, and to syringopeptins, produced by plant-associated pseudomonads. Biofilm growth was least for isolate MCS that grew on plate medium as rough-edged colonies. The patterns of substrate utilization in Biolog plates showed clustering of the Montana isolates compared with Mycobacterium vanbaalenii and Mycobacterium gilvum. CONCLUSION: The five PAH-degrading mycobacterium isolates studied differ in genetic and biochemical properties. SIGNIFICANCE AND IMPACT OF THE STUDY: Different properties with respect to antibiotic susceptibility, substrate utilization and biofilm formation could influence the survival in soil of the microbe and their suitability for use in bioaugmentation.


Subject(s)
Mycobacterium/metabolism , Polycyclic Aromatic Hydrocarbons/metabolism , Soil Microbiology , Anti-Bacterial Agents/pharmacology , Base Sequence , Biodegradation, Environmental , Biodiversity , Biofilms/growth & development , Cell Wall/physiology , Culture Media , DNA, Bacterial/genetics , DNA, Intergenic/genetics , Genes, Bacterial/genetics , Genome, Bacterial/genetics , Molecular Sequence Data , Mycobacterium/drug effects , Mycobacterium/genetics , Phylogeny , Plankton , RNA, Bacterial/genetics , RNA, Ribosomal, 16S/genetics
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