The distribution of the clade specific patterns was extremely significant associated with the tree topology and geographic location of the strains. ∗∗∗ = ( p < 0.0001).
Excerpts
All three analyses showed highly significant interactions between PST and light ( p = 0.0001, p = 0.0002, p = 0.0009, for PST content, production, and C fraction, respectively), a significant interaction between lytic toxicity and whether the strains contained PST ( p = 0.0157 for PST content), and significant effects of lytic toxicity on growth ( p = 0.0125, p = 0.0175, for PST production and C fraction, respectively).
As shown in Figures 3A,B and Table 2 , while both gO GT1c cysteine mutants, gO GT1c-C218S and gO GT1c-C343S, displayed a similar infectivity for HFFs as their parental strains GT1c_1 and GT1c_2, the mutation of C336S in gO GT4 led to reduction in infectivity, which was significant when compared to GT4_1 ( p = 0.0025) and highly significant when compared to GT4_2 ( p < 0.0001).
For instance, decreasing the incubation temperature from 37 to 30°C or room temperature, had a highly significant effect on the total aerobic count for samples collected from the low care zone ( p < 0.0001).
The antagonistic strains had a highly significant effect on fungal growth ( F -value = 26333.5, p < 0.0001) ( Figures 2 , 3 ).
The difference in ciliostasis between the strain-GD-infected group and the control group was highly significant ( p < 0.0001).
By 24 h, highly significant reductions in cytotoxicity were observed with 50 and 200 μg/mL of CIP, LVX, PMB, GEN, OFX and CXM ( P < 0.0001).
However, increasing arsenate concentration had a highly significant effect on normalized growth rate ( p < 0.0001; Figure 3 A).
Statistical analysis using one-way ANOVA confirmed that the differences in biofilm formation between treated and untreated groups were highly significant ( p < 0.0001 for Δ agrA and MRSA).
This observation was confirmed by the two-way PERMANOVA, which crossed swabbed region with health, stating that there were highly significant differences between regions and globally between health states (pseudo- F = 22.241, p -value = 0.0001, pseudo- F = 10.373, p -value = 0.0001, respectively) (Supplementary Table S1 ).
The quadratic model Y = 1.08 + 0.092× 1 + 0.045× 2 + 0.15× 3 –0.13X 1 X 2 –0.14× 1 2 –0.23× 2 2 –0.20× 3 2 was highly significant ( p < 0.0001) and lacked-of-fit was not ( p = 0.197).
Neither inactivation of fumC alone nor combined inactivation with recA altered the adaptability of BW25113, whereas a markedly significant difference was found when the wild-type was compared to Δ aidB and Δ aidB /Δ recA ( p < 0.0001).
For plipastatins, this effect compared with that of the control without lipopeptide was statistically significant ( p = 0.0023, using the Dunn's multiple comparison test) for 300 mg.L −1 of the sample and extremely significant ( p < 0.0001) for the higher concentration (500 mg.L −1 ) of plipastatins.
The differences between time points were highly significant (**** p < 0.0001), reflecting structural maturation of the biofilm ( Figure 6 ).
A Kruskal–Wallis test revealed highly significant differences ( p < 0.0001) in CC distribution between resistant and susceptible groups, indicating a lineage-linked resistance phenotype, and identifying CC31 and CC155 as consistently sensitive.
As shown in Table 5 , the model was highly significant, with an F -value of 30.75 and p < 0.0001, suggesting that it adequately describes the relationship between the independent variables and ZEN lactonase activity.
From Table 9 , it is evident that the model is highly significant ( P < 0.0001), while the lack-of-fit term is not significant ( P > 0.05).
The proportions of these 34 STs were 88.38% in 611 decreased susceptibility to ceftriaxone (CRO-DS) strains and 33.09% in 8,325 background strains, respectively, revealing an extremely significant association between 34 high-frequency STs and CRO-DS ( P < 0.0001).
ANOVA revealed highly significant differences among treatments ( p < 0.0001), and Tukey’s post hoc test confirmed that the combination exhibited significantly higher inhibition compared to salicylic acid ( p < 0.001) and ibuprofen ( p < 0.001) alone, while ibuprofen was also significantly stronger than salicylic acid ( p < 0.001).
Considered separately for Udupi ( Figures 5A,B ) and Shimoga ( Figure 5C,D ), the differences between loads detected in the monsoon season in Udupi (3.47 × 10 3 ; IQR: 1.13 × 10 3 – 1.55 × 10 4 ) and Shimoga (5.02 × 10 3 ; IQR: 3.29 × 10 3 – 1.78 × 10 4 ) compared to the summer season in Udupi (1.55 × 10 3 ; IQR: 1.35 × 10 2 – 4.99 × 10 3 ) and Shimoga (9.18 × 10 2 ; IQR: 5.37 × 10 1 – 1.80 × 10 3 ) were again highly significant ( p = 0.0001 and p < 0.0001, respectively).
The two way ANOVA tests for multiple comparisons showed that the mean differences between the cell lysis data for all three MOIs and control are highly significant ( P < 0.0001).
Likewise, biofilm amount of each strain did not change significantly during assay ( P > 0.05), whereas highly significant ( P < 0.0001) differences in biofilm biomass were found among the assayed strains.
The 1-way ANOVA showed that differences between individual cells of the parallels Nitrate were highly significant for 15 N- and 13 C-enrichments ( p < 0.0001).
Furthermore, a marked elevation of IL-10 was observed in the LR group, reaching a highly significant level ( p < 0.0001). 3.3.
The association between resistant isolates and growing on CIP-containing media was highly significant (Fisher's exact test, p < 0.0001).