Helicobacter pylori virulence genes in the five largest islands of Indonesia

被引:36
作者
Miftahussurur, Muhammad [1 ,2 ,3 ]
Syam, Ari Fahrial [4 ]
Makmun, Dadang [4 ]
Nusi, Iswan Abbas [2 ]
Zein, Lukman Hakim [5 ]
Zulkhairi [5 ]
Akil, Fardah [6 ]
Uswan, Willi Brodus [7 ]
Simanjuntak, David [8 ]
Uchida, Tomohisa [9 ]
Adi, Pangestu [3 ]
Utari, Amanda Pitarini [4 ]
Rezkitha, Yudith Annisa Ayu [3 ]
Subsomwong, Phawinee [1 ]
Nasronudin [3 ]
Yamaoka, Yoshio [1 ,10 ,11 ]
机构
[1] Oita Univ, Fac Med, Dept Environm & Prevent Med, Yufu 8795593, Japan
[2] Airlangga Univ, Fac Med, Dept Internal Med, Gastroenterohepatol Div, Surabaya 60131, Indonesia
[3] Airlangga Univ, Inst Trop Dis, Surabaya 60115, Indonesia
[4] Univ Indonesia, Div Gastroenterol, Dept Internal Med, Fac Med, Jakarta 10430, Indonesia
[5] Univ Sumatera Utara, Div Gastroenterohepatol, Dept Internal Med, Fac Med, Medan 20136, Indonesia
[6] Hasanuddin Univ, Ctr Gastroenterohepatol, Dept Internal Med, Fac Med, Makassar 90245, Indonesia
[7] Santo Antonius Hosp, Dept Internal Med, Pontianak 78115, Indonesia
[8] Yowari Hosp, Dept Internal Med, Jayapura 99352, Indonesia
[9] Oita Univ, Dept Mol Pathol, Fac Med, Yufu 8795593, Japan
[10] Baylor Coll Med, Dept Gastroenterol & Hepatol, Houston, TX 77030 USA
[11] Michael E DeBakey VA Med Ctr, Houston, TX 77030 USA
基金
日本学术振兴会; 日本科学技术振兴机构; 美国国家卫生研究院;
关键词
Helicobacter pylori; Indonesia; Virulence factors; ULCER PROMOTING GENE; GASTRIC-CANCER; ENCODING GLYCOSYLTRANSFERASES; GASTRODUODENAL DISEASES; CYTOTOXIN PRODUCTION; CLINICAL-RELEVANCE; CAGA PROTEIN; VACA; INFECTION; PREVALENCE;
D O I
10.1186/s13099-015-0072-2
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Background: It remains unclear whether the low incidence of gastric cancer in Indonesia is due to low infection rates only or is also related to low Helicobacter pylori pathogenicity. We collected H. pylori strains from the five largest islands in Indonesia and evaluated genetic virulence factors. Methods: The genotypes of H. pylori virulence factors were determined by polymerase chain reaction (PCR)-based sequencing. Histological severity of the gastric mucosa was classified into 4 grades, according to the updated Sydney system. Results: A total of 44 strains were analyzed. Forty-three (97.7 %) were cagA-positive: 26 (60.5 %) were East-Asian-typecag-A, 9 (20.9 %) were Western-type-cagA, and 8 (18.6 %) were novel ABB-type, most of which were obtained from Papuan. EPIYT sequences were more prevalent than EPIYA sequences (P = 0.01) in the EPIYA-B motif of all types of cagA. The majority of cagA-positive strains (48.8 %, 21/43) had a 6-bp deletion in the first pre-EPIYA region. Subjects infected with East-Asian-type-cagA strains with a 6-bp deletion had significantly lower inflammation and atrophy scores in the corpus than those infected with Western-type-cagA strains (both P = 0.02). In total, 70.4 % of strains possessed the vacA s1m1 genotype and 29.5 % were m2. All strains from peptic ulcer patients were of the iceA1 genotype, which occurred at a significantly higher proportion in peptic ulcer patients than that in gastritis patients (55.3 %, P = 0.04). The double positive genotype of jhp0562/beta-(1,3) galT was predominant (28/44, 63.6 %), and subjects infected with this type had significantly higher inflammation scores in the corpus than those with the jhp0562 negative/beta-(1,3) galT positive genotype (mean [median]; 1.43 [1] vs. 0.83 [1], P = 0.04). There were significant differences in cagA and pre-EPIYA cagA type, oipA status, and jhp0562/beta-(1,3) galT type among different ethnic groups (P < 0.05). Conclusions: In addition to a low H. pylori infection rate, the low incidence of gastric cancer in Indonesia might be attributed to less virulent genotypes in predominant strains, which are characterized by the East-Asian-type-cagA with a 6-bp deletion and EPIYT motif, a high proportion of m2, dupA negative or short type dupA, and the jhp0562/beta-(1,3) galT double positive genotype.
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