Quick Search
  Home Journal Information Current Issue Past Issues Services Contact Us  
Articles
Prevalence of Helicobacter pylori resistant to clarithromycin, metronidazole and amoxicillin isolated from pediatric patients in China 
 
Prevalence of Helicobacter pylori resistant to clarithromycin, metronidazole and amoxicillin isolated from pediatric patients in China
  Jin-Dan Yu, Jie Chen, Zhong-Yue Li and Xu-Ping Zhang
 [Abstract] [Full Text] [PDF]   Pageviews: 10503 Times
   

Prevalence of Helicobacter pylori resistant to

clarithromycin, metronidazole and

amoxicillin isolated from pediatric patients in

China

Jin-Dan Yu, Jie Chen, Zhong-Yue Li and Xu-Ping Zhang

Hangzhou, China

Author Affiliations: Department of Gastroenterology, Children's Hospital, Zhejiang University School of Medicine, Hangzhou 310003, China (Yu JD, Chen J, Li ZY and Zhang XP)

Corresponding Author: Jin-Dan Yu, MD, Department of Gastroenterology, Children's Hospital, Zhejiang University School of Medicine, Hangzhou 310003, China (Tel: 86-571-87061007 ext 2443; Fax: 86-571-87084307; Email: yjd0610@163.com)


Background: Antimicrobial resistance in Helicobacter pylori (H. pylori) is an increasing serious problem, and the development of methods for detecting the resistance and the constant surveillance of both prevalence and evolution of H. pylori resistance in children would greatly improve the selection of antibiotics used to treat gastroduodenal infection with this organism. This study was designed to investigate the prevalence of H. pylori resistance to clarithromycin, metronidazole and amoxicillin isolated from pediatric patients in China.

Methods: A total of 44 H. pylori isolates from pediatric patients with gastritis and peptic ulcer undergoing endoscopy were cultured during the period of October 2002 to November 2003 at Children's Hospital, Zhejiang University School of Medicine, Hangzhou, China. The susceptibilities of the 44 H. pylori isolated strains to clarithromycin, metronidazole and amoxicillin were tested by the agar dilution test to determine the minimum inhibitory concentration (MIC).

Results: The range of MIC was as follows: clarithromycin 0.125-64 μg/ml; metronidazole <0.125-128 μg/ml; and amoxicillin <0.125-64 μg/ml. The rate of H. pylori resistant to clarithromycin, metronidazole and amoxicillin in the children was 18.2% (8 strains), 31.8% (14 strains) and 9.1% (4 strains), respectively. Three strains (6.8%) were simultaneously resistant to the 3 antibiotics.

Conclusions: The prevalence of H. pylori resistance to metronidazole is high in children, and the rate of resistance to clarithromycin is higher than that in adults. Amoxicillin-resistant strains are found, and multi-drug-resistant strains of H. pylori to clarithromycin, metronidazole and amoxicillin are also found.

Key words: Helicobacter pylori; susceptibility test; clarithromycin; metronidazole; amoxicillin; children

                   World J Pediatr 2006;1:49-52


Introduction

The emergence of antibiotic resistance is now recognized as a major cause of failure in the eradication of Helicobacter pylori (H. pylori).[1,2] In such patients, in vitro susceptibility testing may be helpful in excluding antibiotic resistance and thereby aids in treatment selection. However, data concerning H. pylori resistance in children are limited. The purpose of this study was to investigate the local primary resistance prevalence by examing in vitro susceptibility of clinical H. pylori against antimicrobial clarithromycin, metronidazole and amoxicillin isolated from pediatric patients during the period of 2002-2003 in Hangzhou, China.

Methods

Bacterial strains

From October 2002 to November 2003, a total of 44 H. pylori strains were isolated from pediatric patients (25 boys, 19 girls; aged 3 to 14 years; mean age, 8.7 years) who had undergone endoscopy at Children's Hospital, Zhejiang University School of Medicine. Biopsy specimens were taken from the gastric antrum or body for testing H. pylori. The diagnoses included gastritis (n=37) and duodenal ulcer (n=7).

Isolation and identification of H. pylori

Fresh gastric biopsy specimens obtained during gastroscopy from symptomatic patients with a positive rapid urease assay were transported to the laboratory in Brucella broth supplemented with 30% glycerol and minced and homogenized, then inoculated immediately on selective medium plates (Columbia agar) enriched with 7%-10% fresh sheep blood and incubated in a microaerophilic environment (CO2 10%, O2 5%, N2 85%) at 37°C for about 3 to 5 days. Suspected isolates were identified as H. pylori by conventional methods using Gram staining and biochemical tests for positive urease, oxidase and catalase activities. All isolates were stored at -70°C in Brucella broth for later determination of antibiotic susceptibility.

Antibiotic susceptibility test

The susceptibilities of H. pylori isolates to clarithromycin, metronidazole and amoxicillin were determined by an agar dilution technique with Mueller-Hinton agar plates supplemented with 5% fresh sheep blood as described by NCCLS recommendations.[3] The bacterial suspension was adjusted to a final concentration of 3×108 CFU/ml. The plates containing serial two-fold dilutions of each antibiotic at concentrations ranging from 0.125 to 128 μg/ml were inoculated with 10 μl of bacterial suspension (approximately 106 CFU) and incubated at 37°C in a microaerophilic environment for 72 hours before reading the minimal inhibitory concentrations (MIC). The antibiotic breakpoints of susceptibility (S) and resistance (R) were determined according to published reports. The breakpoints for clarithromycin used according to the National Committee of Clinical Laboratory Standards (NCCLS) were determined as <1 and 1 μg/ml, respectively. For metronidazole and amoxicillin, these were accepted to be <8 and 8 mg/L, respectively.

Results

MICs range of antibiotic resistance

Table shows the MIC ranges of H. pylori isolates resistant to the 3 antimicrobial agents (clarithromycin, metronidazole and amoxicillin) tested against the total number of strains. The range of MIC varied respectively: clarithromycin 0.125-64 μg/ml; metronidazole <0.125-128 μg/ml; and amoxicillin <0.125-64 μg/ml.

MIC50s (MIC at which 50% of the isolates tested are inhibited) of clarithromycin, metronidazole and amoxicillin were <0.125 μg/ml, 0.5 μg/ml and <0.125 μg/ml respectively, and MIC90s (MIC at which 90% of the isolates tested are inhibited) were 16 μg/ml, 128 μg/ml and 0.5 μg/ml respectively.


Table. Minimal inhibitory concentrations of the three antibiotics for 44 isolates of H. pylrori

MIC (μg/ml)

No. of H. pylori isolates

 

No. of calculative isolates

CLM

AMO

MET

CLM

AMO

MET

<0.125*

33

31

21

33

31

21

0.125

1

0

0

34

31

21

0.25

0

4

0

34

35

21

0.5

2

5

1

36

40

22

1

0

0

3

36

40

25

2

0

0

3

36

40

28

4

0

0

2

36

40

30

8

4

0

0

40

40

30

16

3

3

0

43

43

30

32

0

0

1

43

43

31

64

1

1

3

44

44

34

128

0

0

10

44

44

44


Prevalence of antibiotic resistance

Of all 44 isolates, the rate of H. pylori resistant to clarithromycin, metronidazole and amoxicillin in children was 18.2% (8 strains), 31.8% (14 strains) and 9.1% (4 strains) respectively. Three strains (6.8%) were simultaneously resistant to 3 antibiotics.

Discussion

Triple treatment with a proton-pump inhibitor (PPI) or bismuth salt plus two antibiotics is now commonplace in all patients diagnosed and has been demonstrated to have high eradication rates.[4,5] Clarithromycin, metronidazole and amoxicillin are the most frequently used antibiotics for the treatment of H. pylori infection. However, antibiotic resistance frequently causes failure of eradication of H. pylori. With regard to antibiotic resistance, however, there have been few reports on antibiotic resistance in children, and close attention should be paid by clinicians. It is time to consider routine susceptibility test to guide treatment of individual patient and surveillance of antibiotic resistance.

Previous studies showed that the prevalence of primary resistance to clarithromycin appeared to be lower than 10%,[6] but the rate of clarithromycin resistance has been increasing in recent years and a high prevalence of clarithromycin resistance has also been found in pediatric population. A study conducted during 1993-1996 in Poland[7] revealed that 17% (22/130) of H. pylori strains isolated from children were resistant to clarithromycin, and during 1998-2000 23.5%, showing an increasing resistance over the last 3 years. In a Portuguese study,[8] the rate of clarithromycin resistance was higher in H. pylori isolates from children than in those from adults. It is thought to be associated with that macrolides are now frequently used to treat respiratory infections in children and an increasing overall use of newer macrolides in clinical practice.[9] Our study shows a high level of H. pylori resistance to clarithromycin (18.2%), which is higher than that in adults (5.6%),[10] but an increasing resistance to clarithromycin in adults in China has also been described elsewhere.[11]

Metronidazole resistance is extremely common in H. pylori. A difference in the resistance to metronidazole ranging from 10% to 50% has been found in adult populations from western countries. Higher resistance rates in developing countries varied from 77% to 95%,[12] which were attributed to the extensive use of metronidazole, for instance, in the treatment of parasitic, genital or dental infections. The prevalence of metronidazole-resistant strains in Shanghai, China has been reported to be improved from 42% to 70% during the period of 1995-1999,[13] whereas in some areas reached 90%.[10] The prevalence of metronidazole resistance in our study was 31.8% (14 strains), which was lower than that in adults because of the rare use of metronidazole in children. But all the resistant strains to metronidazole showed a high resistance level with high MIC ranging from 32 to 128 mg/L, the highest being MIC90.

Resistance to amoxicillin has been considered to be low or absent, for example, 0 in pediatric patients in Japan.[14] In recent years, however, reports on the isolates of resistant strains have been increasing worldwide, with a high frequency in particular geogra-phical regions. Dore et al[15] reported the unusually high prevalence of H. pylori resistance to amoxicillin (31% and 45%) with MIC greater than 256 mg/L of all strains. Resistance to amoxicillin was observed in 4 strains (9.1%) of the isolates, reflecting the importance of its use in children in China.

However, three strains (6.8%) were found simul-taneously resistant to clarithromycin, metronidazole and amoxicillin. In Mexico, a study showed an increasing multi-drug-resistant H. pylori strains isolated from children and adults.[16] Lang et al[17] reported that multiple resistance was found in 4.3% (94 strains) of the isolates in Costa Rica. Although it is rare, the appearance of multi-drug-resistant H. pylori strains, especially in children, is of utmost importance, because the eradication of H. pylori infection in similar cases could be a treatment challenge. There is a need for constant surveillance of both prevalence and evolution of H. pylori resistance in children.

Regarding the mechanism of clarithromycin resistance, mutations within domain V of the 23S rRNA gene cause a decreased affinity of clarithromycin for the 23S ribosomal component, resulting in the impaired activity of clarithromycin against H. pylori.[18-21] In contrast to clarithromycin, the mechanisms of resistance to metronidazole in H. pylori are less clear. It has been hypothesized that mutations in the rdxA gene, which encode an oxygen-insensitive NADPH nitroreductase, are responsible for the resistance.[22,23] Some investigators, however, have questioned the mutational inactivation of the rdxA gene and suggested that there are many different pathways for the resistance. Changes in PBP1 have been regarded to be involved in the amoxicillin resistance of H. pylori isolates.[24] A better understanding of antibiotic resistance mechanisms in H. pylori is essential to selecting therapeutic choices and alternative strategies for combating these infections.

In conclusion, we documented a considerable prevalence of H. pylori resistance to commonly used antibiotics such as clarithromycin and metronidazole. Amoxicillin-resistant strain was found and multi-drug-resistant strains which were resistant to the three antimicrobial agents also emerged. We confirmed that implementation of a resistance surveillance program may be advisable in the near future to define resistance and/or multi-drug-resistant patterns of pediatric H. pylori isolates before the selection of a treatment regimen.


Funding: This study was supported by a grant from the Key Project Foundation of Public Health Bureau of Zhejiang Province, China (No. 2003ZD009).

Ethical approval: Not needed.

Competing interest: No benefits in any form have been received or will be received from a commercial party related directly or indirectly to the subject of this article.

Contributors: YJD designed the study and wrote the draft. CJ proposed and directed the study. All authors contributed to the intellectual content of the study and the draft of the paper.


References

1   Georgopoulos SD, Ladas SD, Karatapanis S, Mentis A, Spiliadi C, Artikis V, et al. Factors that may affect treatment outcome of triple Helicobacter pylori eradication therapy with omeprazole, amoxicillin and clarithromycin. Dig Dis Sci 2000;45:63-67.

2   Megraud F. Basis for the management of drug-resistant Helicobacter pylori infection. Drugs 2004;64:1893-1904.

3   National Committee for Clinical Laboratory Standards, Approved standard M100-S10. MIC testing supplemental tables. National Committee for Clinical Laboratory Standards, Wayne, Pa. 2000.

4   Bazzoli F, Pozzato P. Therapy of H. pylori infection. J Physiol Pharmacol 1997;48(Suppl):39-46.

5   Lind T, Megraud F, Unge P, Bayerdorffer E, O'morain C, Spiller R, et al. The MACH2 study: role of omeprazole in eradication of Helicobacter pylori with one-week triple therapies. Gastroenterology 1999;116:248-253.

6   Megraud F, Lehn N, Lind T, Bayerdorffer E, O'Morain C, Spiller R, et al. Antimicrobial susceptibility testing of Helicobacter pylori in a large multicenter trial: the MACH study. Antimicrob Agents Chemother 1999;43:2747-2752.

7   Dzierzanowska-Fangrat K, Rozynek E, Jozwiak P, Celinska-Cedro D, Madalinski K, Dzierzanowska D. Primary resistance to clarithromycin in clinical strains of Helicobacter pylori isolated for children in Poland. Int J Antimicrob Agents 2001;18:387-390.

8   Cabrita J, Oleastro M, Matos R, Manhente A, Cabral J, Barros R, et al. Features and trends in Helicobacter pylori antibiotic resistance in Lisbon area, Portugal (19901999). J Antimicrob Chemother 2000;46:10291031.

9   Kaneko F, Suzuki H, Hasegawa N, Kurabayshi K, Saito H, et al. High prevalence rate of Helicobacter pylori resistance to clarithromycin during long-term multiple antibiotic therapy for chronic respiratory disease caused by non-tuberculous mycobacteria. Aliment Pharmacol Ther 2004;20(Suppl 1): 62-67.

10 Jiang K, Zhang JZ, Pan GZ. Susceptibilities to different antibiotics of Helicobacter pylori strains. Chin J Zoonoses 2000;16:7678.

11 Hao Q, Li Y, Zhang ZJ, Liu Y, Gao H. New mutation points in 23S rRNA gene associated with Helicobacter pylori resistance to clarithromycin in northeast China. World J Gastroenterol 2004;10:10751077.

12 Boyanova L, Stancheva I, Spassova Z, Katzarov N, Mitov I, Koumanova R. Primary and combined resistance to four antimicrobial agents in Helicobacter pylori in Sofia, Bulgaria. J Med Microbiol 2000;49:415-418.

13 Shi T, Liu WZ, Xiao SD, Xu WW. Change of the prevalence of Helicobacter pylori resistance to antibiotics in Shanghai area. Chin J Intern Med 2000;39:576.

14 Kato S, Fujimura S, Udagawa H, Shimizu T, Maisawa S, Ozawa K, et al. Antibiotic resistance of Helicobacter pylori strains in Japanese children. J Clin Microbiol 2002;40:649-653.

15 Dore MP, Osato MS, Realdi G, Mura I, Graham DY, Sepulveda AR. Amoxycillin tolerance in Helicobacter pylori. J Antimicrob Chemother 1999;43:47-54.

16 Torres J, Camorlinga-Ponce M, Perrez-Perez G, Madrazo-De la Garza A, Dehesa M, Gonzalez-Valencia G, et al. Increasing multidrug resistance in Helicobacter pylori strains isolated from children and adults in Mexico. J Clin Microbiol 2001; 39:2677-2680.

17 Lang L, Garcia F. Comparison of E-test and disk diffusion assay to evaluate resistance of Helicobacter pylori isolates to amoxicillin, clarithromycin, metronidazole and tetracycline in Costa Rica. Int J Antimicrob Agents 2004;24:572-577.

18 Versalovic J, Shortridge D, Kibler K, Griffy MV, Beyer J, Flamm RK, et al. Mutations in 23S rRNA are associated with clarithromycin resistance in Helicobacter pylori. Antimicrob Agents Chemother 1996;40:477-480.

19 Stone GG, Shortridhe D, flamm RK, Versalovic J, Beyer J, Idler K, et al. Identification of a 23S rRNA gene mutation in clarithromycin-resistant Helicobacter pylori. Helicobacter 1996;1:227-228.

20 Khan R, Nahar S, Sultana J, Ahmad MM, Rahman M. T2182C mutation in 23S rRNA is associated with clarithromycin resistance in Helicobacter pylori isolates obtained in Bangladesh. Antimicrob Agents Chemother 2004;48:3567-3569.

21 Burucoa C, Landron C, Garnier M, Fauchere JL. T2182C mutation is not associated with clarithromycin resistance in Helicobacter pylori. Antimicrob Agents Chemother 2005; 49:868-870.

22 Marais A, Bilardi C, Cantet F, Mendz GL, Megraud F. Characterization of the genes rdxA and frxA involved in metronidazole resistance in Helicobacter pylori. Res Microbiol 2003;154:137-144.

23 Aldana LP, Kato M, Kondo T, Nakagawa S, Zheng R, Sugiyama T, et al. In vitro induction of resistance to metronidazole, and analysis of mutations in rdxA and frxA genes from Helicobacter pylori isolates. J Infect Chemother 2005;11:59-63.

24 Okamoto T, Yoshiyama H, NakazawaT, Park ID, Chang MW, Yanai H, et al. A change in PBP1 is involved in amoxicillin resistance of clinical isolates of Helicobacter pylori. J Antimicrob Chemother 2002;50:849-856.

Received June 4, 2005; Accepted after revision November 14, 2005

 
  [Articles Comment]

  title Author The End Revert Time Revert / Count

  Username:
  Comment Title: 
 
   

 

     
 
     
World Journal of Pediatric Surgery

roger vivier bags 美女 美女

Home  |  Journal Information  |  Current Issue  |  Past Issues  |  Journal Information  |  Contact Us
Children's Hospital, Zhejiang University School of Medicine, China
Copyright 2007  www.wjpch.com  All Rights Reserved Designed by eb