cagA and vacA status of Spanish Helicobacter pylori clinical isolates.

Helicobacter pylori is a gram-negative rod associated with gastroduodenal pathologies, such as gastritis, peptic ulcer, and gastric adenocarcinoma. Although most H. pylori infections are clinically silent, the organism is associated with substantial morbidity and mortality. It is unknown why the bacteria are able to produce severe disease in some hosts and be innocuous in others. Different virulence factors have been described in H. pylori infection, including urease, lipopolysaccharide, adhesins, and vacuolating cytotoxin (2). The formation of vacuoles is associated with a higher degree of virulence, and two genes, cagA and vacA, have been described to be involved in vacuole production. It is assumed that cagA strains and those with the s1 allele of vacA are more virulent and produce more severe disease than do strains lacking cagA and vacA s2 strains. Recently, Rudi et al. (5) published a study on cagA and vacA genes and their relationship to the production of several gastroduodenal diseases. They studied 65 strains by PCR (43 from gastritis, 19 from peptic ulcer, and 3 from cancer patients) and found a prevalence of the cagA gene of 84.2% in peptic ulcer and 67.4% in gastritis strains. When the vacA gene was studied, the s1 allele was found to be more prevalent in strains from patients with peptic ulcers (100% showed this allele) and the s2 allele was found only in strains from patients with gastritis. They also found a strong association between the presence of the cagA gene and the s1 allele of vacA. Recently, we isolated 104 Spanish H. pylori strains, 69 from peptic ulcer patients and 35 from gastritis patients, and aimed to study cagA and vacA status and the relationship with specific pathologies. Antral biopsy specimens were cultured onto blood agar plates (Columbia agar plus 5% horse blood) and incubated for 10 days under microaerobic conditions at 37°C. H. pylori was identified by colony morphology, Gram strain, and positive urease, catalase, and oxidase test results. We performed two PCRs in order to detect the cagA gene and the s1 or s2 allele of the vacA gene. DNA was extracted by the CTAB method (6). cagA was detected by applying a protocol described by Covacci and Rappuoli (3) using primers D008 (59ATAATGCTAAATTAGACAACTTGAGCGA-39) and R008 (59-TTAGAATAATCAACAAACATCACGCCAT-39 to detect a 297-bp amplified fragment. For the study of vacA, the protocol of Atherton (1) was performed by using two primers (VA1-F, 59-ATGGAAATACAACAAACACAC-39, and VA1-R, 59-CTGCTTGAATGCGCCAAAC-39) and two fragments of 259 and 286 bp corresponding to the s1 and s2 alleles were detected. Results were studied by 2% agarose gel electrophoresis and visualized in a UV transilluminator. cagA and vacA detections are shown in Figs. 1 and 2. We agree with Rudi et al. about the prevalence of s1 among cagA strains; however, we found a smaller percentage (64.1 versus 87.0%) and we detected four strains that lacked cagA and possessed the s1 allele of vacA, a genotype which was not found by those authors. When we studied the relationship