Skip to main content
Advertisement
Browse Subject Areas
?

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

< Back to Article

Table 1.

Bacterial strains used in this study.

More »

Table 1 Expand

Table 2.

Primers and their concentrations in multiplex PCR.

More »

Table 2 Expand

Table 3.

Oligonucleotide probes used in this study.

More »

Table 3 Expand

Figure 1.

Probe positions on the microarray.

OA-1993, the positive control probe based on the 16S rRNA gene. WL-4006, the negative control probe. Cy3, the positional reference and printing control probe. Blank, 50%DMSO. The rest are the specific probes for the target strains.

More »

Figure 1 Expand

Figure 2.

Unrooted phylogenetic trees constructed by the neighbor-joining method based on the ITS-tRNAAla and ITS-tRNAIle genes.

Bootstrap values were based on 1,000 replications and only values greater than 50% are shown. A, Unrooted ITS-tRNAAla gene phylogenetic tree of Legionella spp. and subspp. constructed with the neighbor-joining method. B, Unrooted ITS-tRNAIle gene phylogenetic tree of Legionella spp. and subspp. constructed with the neighbor-joining method.

More »

Figure 2 Expand

Figure 3.

Microarray differentiation of the Legionella spp.

L. pneumophila; (2) L. anisa; (3) L. bozemanii; (4) L. dumoffii; (5) L. fairfieldensis; (6) L. gormanii; (7) L. jordanis; (8) L. longbeachae; (9) L. micdadei; (10) L. maceachernii; (11) L. anisa and L. dumoffii; (12) L. anisa and L. longbeachae; (13) L. fairfieldensis, L. gormanii and L. jordanis; and (14) L. longbeachae, L. maceachernii and L. micdadei.

More »

Figure 3 Expand