Primary clarithromycin resistance in Italy assessed on Helicobacter pylori DNA sequences by TaqMan real-time polymerase chain reaction

被引:63
作者
De Francesco, V
Margiotta, M
Zullo, A
Hassan, C
Valle, ND
Burattini, O
Cea, U
Stoppino, G
Amoruso, A
Stella, F
Morini, S
Panella, C
Ierardi, E
机构
[1] Univ Foggia, Osped Riuniti, Dept Med Sci, Gastroenterol Sect, I-71100 Foggia, Italy
[2] Univ Bari, Gastroenterol Sect, Dept Emergency & Organ Transplantat, Bari, Italy
[3] Osped Nuovo Regina Margherita, Rome, Italy
[4] Osped Riuniti Foggia, Gastroenterol Unit, Foggia, Italy
[5] San Giacomo Hosp, Pathol Unit, Rome, Italy
关键词
D O I
10.1111/j.1365-2036.2006.02769.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background Helicobacter pylori clarithromycin resistance is increasing worldwide and different mutations are involved in its mechanisms. Recently, molecular methods have been proposed to assess these mutations. Aim To assess prevalence of primary clarithromycin resistance in two Italian areas, and the distribution of involved mutations, by using a novel method for real-time polymerase chain reaction. Methods Two hundred and thirty-two H. pylori-positive patients undergoing oesophagogastroduodenoscopy in two Italian towns (Rome, centre Italy; Foggia, south Italy) were enrolled. Helicobacter pylori infection was detected by histology, rapid urease and urea breath tests. Clarithromycin resistance was assessed by TaqMan real-time polymerase chain reaction on paraffin-embedded antral biopsies. Results Primary clarithromycin resistance was detected in 62 (26.7%) patients. Its prevalence did not differ between the two areas (31.5%, centre vs. 23.3%, south; P = 0.17) and between non-ulcer dyspepsia and peptic ulcer patients (28.4% vs. 20.7%, P = 0.2). The A2143G point mutation was detected in 35 (56.4%) patients, A2142G in 14 (22.6%), A2142C in eight (12.9%), whilst a double mutation (A2143G plus A2142C or A2142G) was present in the remaining five (8.1%) cases. Conclusions Our study found that primary clarithromycin resistance is highly prevalent in both central and southern Italy, and that A2143G is the most frequent point mutation involved in these areas.
引用
收藏
页码:429 / 435
页数:7
相关论文
共 34 条
[1]   Efficient priming of PCR with short oligonucleotides conjugated to a minor groove binder [J].
Afonina, I ;
Zivarts, M ;
Kutyavin, I ;
Lukhtanov, E ;
Gamper, H ;
Meyer, RB .
NUCLEIC ACIDS RESEARCH, 1997, 25 (13) :2657-2660
[2]   cagA status and eradication treatment outcome of anti-Helicobacter pylori triple therapies in patients with nonulcer dyspepsia [J].
Broutet, N ;
Marais, A ;
Lamouliatte, H ;
De Mascarel, A ;
Samoyeau, R ;
Salamon, R ;
Mégraud, F .
JOURNAL OF CLINICAL MICROBIOLOGY, 2001, 39 (04) :1319-1322
[3]   Clarithromycin and amoxicillin susceptibility of Helicobacter pylori strains isolated from adult patients with gastric or duodenal ulcer in Italy [J].
Franzin, L ;
Pennazio, M ;
Cabodi, D ;
Rossini, FP ;
Gioannini, P .
CURRENT MICROBIOLOGY, 2000, 40 (02) :96-100
[4]   European Multicentre survey of in vitro antimicrobial resistance in Helicobacter pylori [J].
Glupczynski, Y ;
Mégraud, F ;
Lopez-Brea, M ;
Andersen, LP .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 2001, 20 (11) :820-823
[5]  
Houben MHMG, 1999, ALIMENT PHARM THER, V13, P1047
[6]   Mutations in the 23S rRNA gene of Helicobacter pylori associated with clarithromycin resistance [J].
Kim, KS ;
Kang, JO ;
Eun, CS ;
Han, DS ;
Choi, TY .
JOURNAL OF KOREAN MEDICAL SCIENCE, 2002, 17 (05) :599-603
[7]  
Kist M., 2003, Helicobacter, V8, P465
[8]   Gastric mucosal density of Helicobacter pylori estimated by real-time PCR compared with results of urea breath test and histological grading [J].
Kobayashi, D ;
Eishi, Y ;
Ohkusa, T ;
Ishige, I ;
Suzuki, T ;
Minami, J ;
Yamada, T ;
Takizawa, T ;
Koike, M .
JOURNAL OF MEDICAL MICROBIOLOGY, 2002, 51 (04) :305-311
[9]   Oligonucleotides with conjugated dihydropyrroloindole tripeptides: base composition and backbone effects on hybridization [J].
Kutyavin, IV ;
Lukhtanov, EA ;
Gamper, HB ;
Meyer, RB .
NUCLEIC ACIDS RESEARCH, 1997, 25 (18) :3718-3723
[10]   Fast and accurate quantitative detection of Helicobacter pylori and identification of clarithromycin resistance mutations in H-pylori isolates from gastric biopsy specimens by real-time PCR [J].
Lascols, C ;
Lamarque, D ;
Costa, JM ;
Copie-Bergman, C ;
Le Glaunec, JM ;
Deforges, L ;
Soussy, CJ ;
Petit, JC ;
Delchier, JC ;
Tankovic, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (10) :4573-4577