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Acidovorax citrulli can be divided into two genetic groups: group I and group II based primarily on pulsed-field gel electrophoresis ( PFGE) and multilocus sequence classification ( MLST). To distinguish more rapidly between strains of the two groups, a pair of specific primer for specific polymerase chain reaction ( PCR) that can identify group II strains was designed based on the pilL gene of a group II strain, AAC00-1. PCR results showed that a 332-bp band was generated for 51 of 52 group II strains whereas only three of 93 group I strains were positive, largely consisting with previous studies of A. citrulli classification. Results of PCR showed the primers were able to detect group II strains of A. citrulli and distinguish between strains of groups I and II rapidly and accurately. [ABSTRACT FROM AUTHOR]

Aim: To find suitable solutions having lesser granules and keeping erythrocytes in normal shapes under atomic force microscopy (AFM)., Methods: Eight kinds of solutions, 1% formaldehyde, PBS buffer (pH7.2), citrate buffer (pH 6.0), 0.9% NaCl, 5% dextrose, TAE, 1640 medium and 5% EDTA-K2, were selected from commonly used laboratory solutions, and venous blood from a healthy human volunteer was drawn and anticoagulated with EDTA-K2. Before scanned by AFM (NanoScopeIIIa SPM, Digital Instruments, Santa Barbara, CA), a kind of intermixture was deposited on freshly cleaved mica and then dried in the constant temperature cabinet (37 degrees)., Results: One percent formaldehyde, citrate buffer, 5% dextrose, TAE, were found to keep human erythrocytes in normal shape with few particles. Processed by these solutions, fine structures of human erythrocyte membrane were obtained., Conclusion: One percent formaldehyde, citrate buffer, 5% dextrose and TAE may be applied to dispose erythrocytes in AFM. The results may offer meaningful data for clinical diagnosis of blood by AFM.