4 to 40 1% of IGS-T-RFs present in nodules were detected in the r

4 to 40.1% of IGS-T-RFs present in nodules were detected in the respective soil sample. Figure 4 shows the similarity relationships between IGS-T-RFLP profiles. Non-metric MDS plot of IGS-T-RFLP profiles (Figure 4a) showed a possible separation of nodule and soil populations Rigosertib on the second dimension. In particular, the nodule population in pot 1 was more separated from the soil population of the same pot and from the populations of the other pots. On the contrary, nodule populations of pots 2 and 3 were the closest ones,

with soil population of pot 3 in the same cluster (Figure 4b), suggesting a possible effect of plant genotype as previously shown [23, 36]. However, in agreement with the Selinexor order high number of single-sample haplotypes detected, an AMOVA carried out to evaluate the selleckchem variance contribution to a hypothetical differentiation

of soil and nodule S. meliloti population showed that 17.37% only of variance was attributed to a soil-nodule separation, the remaining 82.63% of variance being due to among-nodules and among-soil differences. Additionally, no statistical significant separation (P < 0.46) was detected for groupings based on the two plant genotypes present in the mesocosms. Figure 4 a) Non-metric MDS plot of similarities of IGS-T-RFLP profiles from S. meliloti population analysis. a) The pattern of similarity of S. meliloti populations has been inspected by using Non-metric Multidimensional scaling (N-MDS) based on Jaccard similarity matrix. Stress Anidulafungin (LY303366) = 0.0898. b) Cluster analysis based on Jaccard similarity matrix. Scale bar represents Jaccard similarity coefficient Discussion In recent years

there has been an increasing interest in exploring the bacterial flora associated with plants [37–41]. A recent field survey indicates [8] that plant aerial parts (leaves) harbor complex, but highly variable, bacterial communities, and that only a small number of bacterial taxa (mainly belonging to Alphaproteobacteria) are plant-specific. In the experiments reported here, as in the majority of the reports on endophytic microflora, we refer to endophytic and epiphytic bacteria indicating all those that are inside the plant tissue or strongly adhering to the plant surface, such as they resist washing and sterilization (or their DNA is retained by plant tissue), therefore a more correct definition could be “plant-associated bacteria”. The present study shows that root nodules and aerial parts of Medicago sativa plants grown in mesocosm conditions, harbor distinct bacterial communities with specific signatures at the class, family and species levels and that these communities do not mirror soil bacterial communities.

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