Viable cells from two different bacterial species, namely Escherichia coli and Beijevinckia derxii were enumerated by three different operators using the Drop and the Spread methods. Statistical analysis showed that counts obtained by the two methods were significantly different only for B. derxii, probably due to the influence of the extracellular slime layer that promotes the formation of cell clusters. Statistically significant differences were also observed when comparing results from the three operators.ESCOLA PAULISTA MED,DEPT BIOSTAT,São Paulo,BRAZILESCOLA PAULISTA MED,DEPT BIOSTAT,São Paulo,BRAZILWeb of Scienc
Bacterial growth is often difficult to estimate beyond classical cultivation approaches. Low cell nu...
<p>Data for the crusts (eight libraries combined; red), sediments (six libraries combined; green), a...
It is generally conceded that the degree of precision ordinarily attained with dilution plate counti...
Drop plate technique has a priority and preference compared with the spread plate procedure, because...
Background: Accurate quantitative analysis of microorganisms is recognized as an essential tool for ...
Biofilms forming on the surface of indwelling medical devices by microorganisms such as Staphylococc...
<p>These genotypes or isolates were sorted into 7 different bacterial groups, including total bacter...
<p>a) Absolute abundance of bacterial species in queen samples subdivided by mating and isolation st...
<p>Quantitative differences between clustering methods.</p> <p>A. Differences in total OTU counts wh...
The common practice of counting bacteria using epifluorescence microscopy involves selecting 5–30 ra...
THE method of Miles, Misra and Irwin (1938) has for many years been the standard tech-nique for the ...
<p>(A) Bacterial biofilm density (bact cm<sup>-2</sup>) on different shells. (B) The relative size (...
Microbial communities are the common mode of existence of bacteria in their natural habitats. As suc...
For ANCOM procedure, the clr (centered log ratio) table of ASVs grouped by genera was used, which wa...
(A) Pangenome sizes as a function of the number of genomes analyzed for the BSI (912 strains) and co...
Bacterial growth is often difficult to estimate beyond classical cultivation approaches. Low cell nu...
<p>Data for the crusts (eight libraries combined; red), sediments (six libraries combined; green), a...
It is generally conceded that the degree of precision ordinarily attained with dilution plate counti...
Drop plate technique has a priority and preference compared with the spread plate procedure, because...
Background: Accurate quantitative analysis of microorganisms is recognized as an essential tool for ...
Biofilms forming on the surface of indwelling medical devices by microorganisms such as Staphylococc...
<p>These genotypes or isolates were sorted into 7 different bacterial groups, including total bacter...
<p>a) Absolute abundance of bacterial species in queen samples subdivided by mating and isolation st...
<p>Quantitative differences between clustering methods.</p> <p>A. Differences in total OTU counts wh...
The common practice of counting bacteria using epifluorescence microscopy involves selecting 5–30 ra...
THE method of Miles, Misra and Irwin (1938) has for many years been the standard tech-nique for the ...
<p>(A) Bacterial biofilm density (bact cm<sup>-2</sup>) on different shells. (B) The relative size (...
Microbial communities are the common mode of existence of bacteria in their natural habitats. As suc...
For ANCOM procedure, the clr (centered log ratio) table of ASVs grouped by genera was used, which wa...
(A) Pangenome sizes as a function of the number of genomes analyzed for the BSI (912 strains) and co...
Bacterial growth is often difficult to estimate beyond classical cultivation approaches. Low cell nu...
<p>Data for the crusts (eight libraries combined; red), sediments (six libraries combined; green), a...
It is generally conceded that the degree of precision ordinarily attained with dilution plate counti...