Volume 16, Number 6—June 2010
Clonal Expansion of Multidrug-Resistant and Extensively Drug-Resistant Tuberculosis, Japan
The emergence and spread of multidrug-resistant (MDR) and extensively drug-resistant (XDR) tuberculosis (TB) has raised public health concern about global control of TB. To estimate the transmission dynamics of MDR and XDR TB, we conducted a DNA fingerprinting analysis of 55 MDR/XDR Mycobacterium tuberculosis strains isolated from TB patients throughout Japan in 2002. Twenty-one (38%) of the strains were classified into 9 clusters with geographic links, which suggests that community transmission of MDR/XDR TB is ongoing. Furthermore, the XDR M. tuberculosis strains were more likely than the non–XDR MDR strains to be clustered (71% vs. 24%; p = 0.003), suggesting that transmission plays a critical role in the new incidence of XDR TB. These findings highlight the difficulty of preventing community transmission of XDR TB by conventional TB control programs and indicate an urgent need for a more appropriate strategy to contain highly developed drug-resistant TB.
The epidemic of drug-resistant tuberculosis (TB) has raised public health concern about the global control of TB. The World Health Organization estimated that 0.5 million cases of multidrug-resistant TB (MDR TB) (i.e., Mycobacterium tuberculosis resistant to >2 of the most potent TB drugs, rifampin and isoniazid) occurred in 2007 (1). Some countries have extraordinarily high rates of this disease, but the problem is universal, and the extent varies from 1 country to another.
Another recent alarming issue is the emergence of extensively drug-resistant TB (XDR TB) (i.e., M. tuberculosis with MDR plus resistance to any fluoroquinolone and >1 injectable drug, thus posing even greater management challenges than MDR TB alone). The treatment outcome of XDR TB is worse than that of simple MDR TB, and the death rate is particularly high among HIV-infected patients (2). Also, because XDR TB is much more expensive to manage in terms of prolonged medication and prolonged period of infectivity to other persons (3), it has the potential to exhaust human and financial resources of the public health system for TB control. Although this new life-threatening disease had been reported from 49 countries as of June 2008 (4), its transmissibility among immunocompetent persons is not well known (5).
In Japan, TB remains a major infectious disease; in 2008, a total of 19.4 cases/100,000 population were reported (6), and Japan is generally classified as a country with intermediate TB incidence. According to the most recent nationwide drug-resistance survey, the prevalence of MDR TB and XDR TB were 1.9% and 0.5%, respectively (7). Approximately one third of MDR and XDR (MDR/XDR) M. tuberculosis strains were isolated from new TB patients, implying ongoing transmission of MDR/XDR TB in Japan.
Our purpose was to evaluate the transmission dynamics of MDR/XDR TB by using strains from the most recent (2002) nationwide drug-resistance survey in Japan, an industrialized country with low HIV incidence and intermediate TB incidence. We did so by analyzing the MDR/XDR strains by molecular genotyping methods, i.e., insertion sequence 6110 restriction fragment length polymorphism (IS6110-RFLP), spacer-oligonucleotide genotyping (spoligotyping), and variable number tandem repeats (VNTR).
We used data and culture isolates obtained in the 2002 nationwide drug-resistance survey, as previously reported (7). Briefly, during June–November 2002, a total of 3,122 clinical strains were collected from different patients who had started treatment in 99 hospitals throughout Japan. The number of patients enrolled represented 36.0% of all new reported TB cases during the study period. The sampling of the hospital was not randomized but was based on voluntary participation. The survey identified 60 MDR/XDR M. tuberculosis strains, 55 of which were analyzed in this study; the other 5 strains were unavailable for use in this study.
We used patient information collected from a standard data collection form in the drug-resistance survey in 2002 (7). The information included demographic data (age, sex, nationality, hospital, geographic area of the hospital), clinical data (history of TB treatment, site of TB disease, chest radiograph findings, underlying disease), and bacteriologic data (results of sputum smear test for acid-fast bacilli). Patients were classified as new if they had never been treated for TB for >4 weeks and as previously treated if they had ever been treated for TB for >4 weeks. The survey protocol conformed to the national guidelines for epidemiologic research (8).
Drug Susceptibility Testing
Drug susceptibility testing was performed at the Research Institute of Tuberculosis, Tokyo, by using the proportion method on standard 1% Ogawa egg-based slants (7) and the following drug concentrations: isoniazid 0.2 µg/mL, rifampin 40 µg/mL, streptomycin 10 µg/mL, ethambutol 2.5 µg/mL, ethionamide 20 µg/mL, kanamycin 20 µg/mL, cycloserine 30 µg/mL, p-aminosalicylic acid 0.5 µg/mL, and levofloxacin 1 µg/mL. Pyrazinamide susceptibility was tested by using MGIT AST (Becton Dickinson, Sparks, MD, USA) at a concentration of 100 µg/mL. All compounds were obtained from Sigma (St. Louis, MO, USA).
Definition of XDR TB
We defined XDR strains according to the World Health Organization definition of XDR (1) and drug availability for TB treatment in Japan. XDR strains were defined as M. tuberculosis strains with resistance to at least isoniazid, rifampin, levofloxacin, and kanamycin.
Three molecular genotyping methods based on IS6110-RFLP, spoligotyping, and VNTR were performed on the 55 MDR/XDR strains. IS6110-RFLP typing was performed according to the standardized protocol (9). The RFLP band patterns were compared by using the BioNumerics software package version 5.1 (Applied Maths, Kortrijk, Belgium). Strains with an identical band pattern were classified as an RFLP cluster. Spoligotyping was also performed according to the standard protocol (10). Classification of the spoligotype family was performed according to the international database, SpolDB4 (11). The VNTR analysis was conducted as described elsewhere (12) by using the standard 15 mycobacterial interspersed repetitive unit–VNTR proposed by Supply et al. (13), i.e., VNTRs 0424, 0577, 0580, 0802, 0960, 1644, 1955, 2163b, 2165, 2401, 2996, 3192, 3690, 4052, and 4156 plus 4 other loci, VNTRs 2074, 2372, 3155, and 3336. The latter 4 loci were added to increase discrimination for the Beijing family strains because of their high prevalence in Japan (12).
Statistical analysis was performed with Epi Info software 3.51 (Centers for Disease Control and Prevention, Atlanta, GA, USA), by using χ2 test or Fisher exact test for the comparison of proportions. A p value <0.05 was considered significant.
Epidemiologic Characteristics of Patients
A total of 55 MDR/XDR cases were analyzed. The characteristics of patients with MDR/XDR TB are summarized and compared with those of patients with pansusceptible strains (n = 2,782) in Table 1. Patients with MDR/XDR TB were significantly more likely to be younger (odds ratio [OR] 5.69 for age 21–40 years; 4.11 for age 41–60 years) and foreigners (OR 6.41) and to have been previously treated (OR 10.55). All MDR/XDR TB patients had pulmonary disease, and these patients were significantly more likely to have cavitary lesions (OR 3.24) and to have positive sputum smear test results (OR 2.20).
Of the 55 MDR/XDR TB cases, 17 (31%) were XDR TB. We found no significant differences between patients with XDR TB and patients with MDR but not XDR (non–XDR MDR) TB. XDR TB patients tended to be female, although the difference was not statistically significant (p = 0.06, Fisher exact test).
Analysis by Spoligotyping
We performed spoligotyping to determine the population structure of the 55 MDR/XDR strains (Table 2). The most dominant spoligotype family in the MDR/XDR cases was the Beijing family genotype (62%, n = 34), followed by the T (13%, n = 7), Latino-American and Mediterranean (5%, n = 3), U (2%, n = 1), East-African Indian (2%, n = 1), and X (2%, n = 1) family genotypes. Eight (15%) strains were unclassified according to the database.
The proportion of the Beijing family, which is frequently reported to be associated with drug resistance (14), did not significantly differ between the non–XDR MDR M. tuberculosis strains and XDR M. tuberculosis strains (68% vs. 47%; p = 0.14), and distribution of the other spoligotype families did not differ significantly (data not shown).
Cluster Analysis by IS6110-RFLP
All 55 MDR/XDR strains were genotyped by IS6110-RFLP, and 21 (38%) were classified into 9 clusters, each with identical RFLP patterns (clusters 1–9) (Appendix Figure). All members of each cluster belonged to the same spoligotype family. The remaining 34 strains exhibited unique RFLP patterns. Cluster size ranged from 2 to 4, and 7 clusters had 2 members, 1 with 3 members and 1 with 4 members. IS6110 copy numbers ranged from 1 to 18. Four (7%) strains had <5 copies of IS6110, and these strains were discriminated as unique strains by the subsequent VNTR analysis. Of the 21 RFLP-clustered strains, 13 (62%) were classified as XDR M. tuberculosis, and 8 (38%) were isolated from new TB patients. Of the 17 XDR M. tuberculosis strains, 4 were resistant to all drugs tested, and 2 belonged to cluster 8. Among the 9 RFLP-clusters, 7 were from Japanese patients exclusively; the other 2 clusters were from both Japanese and foreign-born patients.
Cluster Analysis by VNTR
The results of the 19-locus VNTR (15 mycobacterial interspersed repetitive unit–VNTR + additional 4 loci) analysis showed that 7 of the 9 RFLP-clusters were identical according to the 19-locus VNTR (Appendix Figure). A difference in only 1 locus was observed in the remaining 2 RFLP-clusters: 1 at VNTR1955 in cluster 6, and 1 at VNTR2163b in cluster 9 (Appendix Figure).
Geographic Distribution of Hospitals with MDR/XDR TB Patients among Each Cluster
To estimate the possible clonal expansion of MDR/XDR TB in communities, we compared the geographic areas of patients’ hospitals among each cluster (Table 3). The 55 MDR/XDR TB patients were treated by 23 hospitals, which were located in 16 of the 47 prefectures in Japan. Of the 9 clusters, 7 consisted of patients whose hospitals were located in the same or neighboring prefectures, and the remaining 2 clusters consisted of patients whose hospitals were located in the same region (i.e., a geographic and administrative area with several prefectures). Clusters with geographic links suggest the clonal expansion of MDR/XDR TB occurred in local areas. Although patients in clusters 4 and 7 were from the same hospital, further information about their contact was unavailable because an epidemiologic survey was not performed.
Characteristics of Clustered Cases
We analyzed the associations of genetic clustering by IS6110-RFLP with patients’ characteristics and bacteriologic factors (Table 4). XDR TB occurred more frequently among the clustered cases than among the unique cases (OR 7.73), but differences between the 2 groups were not significant for any of the remaining factors i.e., age, sex, nationality, treatment history, site of TB disease, chest radiographic findings, sputum-smear test results, underlying disease, or member of the Beijing family genotype.
Our study described the transmission dynamics of MDR/XDR TB in Japan on a national scale. Analysis of the 55 MDR/XDR TB cases showed that MDR/XDR TB was more frequent among younger patients, previously treated patients, and foreign-born patients than among patients with drug-susceptible TB (Table 1). In addition, the XDR TB cases, which represented 31% of the total MDR TB cases, were more likely to be associated with clustering than were the non–XDR MDR TB cases (Table 4), suggesting that ongoing transmission plays a critical role in new cases of XDR TB. We also found that the Beijing family genotype predominated in MDR/XDR M. tuberculosis (Table 2) and in drug-susceptible M. tuberculosis in this setting (12).
Although IS6110-RFLP analysis has been the standard for strain typing in studies of M. tuberculosis transmission, false clusters comprising strains without any epidemiologic link, and thus not reflecting clonal transmission, have been reported (15–17). This use of IS6110-RFLP analysis is especially problematic in area in which strains with stable RFLP patterns are endemic (18,19). In this context, because of its post hoc nature, a limitation of our study is its lack of information about epidemiologic links among clustered patients.
We therefore evaluated the genetic clonality of RFLP-clustered strains more rigorously by using the 19-locus VNTR. Our previous study demonstrated that most of the RFLP-clustered strains without epidemiologic links were discriminated by the 19-locus VNTR (12). In this study, the results correlated strongly between RFLP and VNTR in terms of cluster formation; 7 of the 9 RFLP-clusters had completely identical 19-locus VNTR profiles (Appendix Figure). Each of the remaining 2 clusters contained a single-locus variant, i.e., the difference was at only 1 locus of 1 strain in each cluster. This minor difference in VNTR profile is highly likely to have occurred as a random variation in strains from the same source, as argued by several investigators (13,20). In addition to analyzing by RFLP and VNTR, we confirmed that all of the 9 clusters shared identical mutations on drug resistance genes for rifampin and isoniazid (i.e., rpoB and katG, respectively, data not shown).
Geographic distribution of the hospitals also supports the clonal expansion of MDR/XDR TB (Table 3). Isolation of most of the clustered strains from hospitals in the same or neighboring prefectures may indicate that transmission is occurring in the communities. Furthermore, we assume that some of the clustering in our study did not result from direct transmission among the members but rather resulted from exposure of the members to a common infection source or infection with different sources sharing a near ancestor. The discordance of drug resistance other than isoniazid and rifampin resistance among clusters implies that the stepwise acquisition of drug resistance had occurred chronologically during successive transmissions (Appendix Figure). Thus, all these findings support the assumption of ongoing community transmissions of MDR/XDR TB.
A high proportion (71%, 12/17) of the XDR strains were involved in clusters, a finding consistent with the results of a hospital-based study in Osaka, Japan (21). Of the 12 clustered cases, 4 were new cases and 8 were among previously treated patients. The clustered XDR TB cases among the new cases strongly indicated that these persons had been primarily infected with XDR M. tuberculosis strains. Also, TB may have developed in the clustered XDR TB patients with previous TB treatment as a result of exogenous reinfection with XDR TB, as described in a report of fatal TB in a patient infected with an MDR strain when his disease had been almost cured (22).
One possible explanation for the high clustering rate of XDR TB is that new cases of XDR TB are more likely to be caused by transmission than by acquisition of multiple drug resistance as a result of treatment failure. Shah et al. reported that patients with XDR TB were more likely than those without XDR TB to be infectious in terms of duration and proportion of sputum smear positivity (3). Furthermore, at least 142 non–XDR MDR TB and 180 XDR TB patients were reported to be in Japan as of 2000 (23). All were culture positive, and a considerable number were treated as outpatients despite their infectiousness and drug resistance. Thus, we assume that some of those patients with chronic MDR/XDR TB may have played a role as a source of transmission, as described in this study.
Because these findings and our cluster analysis suggest that the current TB control strategy is insufficient to prevent community transmission of MDR/XDR TB, more detailed investigations of MDR/XDR TB transmission based on contact tracing are urgently needed to improve the infection control strategy, including an isolation policy for highly infectious patients with refractory drug-resistant strains. At the same time, ethical issues, such as the human rights of these patients, should be carefully considered.
Only a few cases of XDR TB transmission have ever been reported. A large group of XDR TB cases, mainly among HIV-infected patients, was reported in South Africa (2). Another study in South Africa reported 12 cases of exogenous reinfection with XDR TB (24). In Iran, DNA fingerprinting analysis suggested 2 outbreaks of XDR TB involving 12 patients in 1 family and their close contacts (25). In Norway, a patient who was lost to follow-up has been transmitting an XDR M. tuberculosis strain for 12 years, and that transmission has ultimately resulted in 15 XDR TB cases (26). Consistent with these previous reports, our study has added novel evidence for clonal expansion of XDR M. tuberculosis strains even in an industrialized country with intermediate TB incidence and low incidence of HIV.
Another limitation of this study is a possible sampling bias, which could be caused by the following factors. First, the sampling of the survey participants was not randomized but was based on voluntary participation of the hospitals, which may be likely to include more serious TB cases (7). Second, the sampling fraction is low (38%) and the study period is short (6 months), either of which may produce a biased subset of the total cases. In addition, the low sampling fraction and the short study period may lead to reduced clustering of cases (27,28). A more complete understanding of transmission dynamics of MDR/XDR TB requires a real-time DNA fingerprinting method such as VNTR on a nationwide scale.
Four strains from the 55 MDR/XDR TB cases were identified as totally drug-resistant strains (29), indicating that they were resistant to all 10 drugs tested (Appendix Figure). Of these strains, 2 in 1 cluster (cluster 8) were from new cases, and both patients were women in their 20s who were full-time workers and had no underlying disease. Both patients were registered in the same area (no further data available); TB as formidable as totally drug-resistant TB can affect otherwise healthy young adults even on a mass basis.
The results of this study showed that transmission of MDR TB, especially XDR TB, is currently occurring in communities of Japan. Further studies to prospectively identify the transmission route through contact tracing and real-time DNA fingerprinting methods on a population basis are required. Although the MDR/XDR TB problem is not great in Japan, our findings highlight the relevance of proper infection control, as well as effective treatment, to further contain highly developed drug-resistant TB.
Dr Murase is a microbiologist at the Molecular Epidemiology Division of the Research Institute of Tuberculosis, Tokyo, Japan. His primary research interests include molecular epidemiology, drug resistance, and international control of tuberculosis.
We are sincerely grateful to the members of the Tuberculosis Research Committee (RYOKEN) for the collection of TB strains. We thank Toru Mori for his valuable review of the manuscript.
This study was partly funded by the research project on M. tuberculosis in the “Emerging and Reemerging Infectious Diseases Research Fund,” Ministry of Health, Labour and Welfare, Japan (principal investigator, Seiya Kato).
- World Health Organization. Anti-tuberculosis drug resistance in the world: fourth global report (WHO/HTM/TB/2008.394); 2008 [cited 2010 Feb 10]. http://whqlibdoc.who.int/hq/2008/WHO_HTM_TB_2008.394_eng.pdf
- Gandhi NR, Moll A, Sturm AW, Pawinski R, Govender T, Lalloo U, Extensively drug-resistant tuberculosis as a cause of death in patients co-infected with tuberculosis and HIV in a rural area of South Africa. Lancet. 2006;368:1575–80.
- Shah NS, Pratt R, Armstrong L, Robison V, Castro KG, Cegielski JP. Extensively drug-resistant tuberculosis in the United States, 1993–2007. JAMA. 2008;300:2153–60.
- Raviglione MC. Facing extensively drug-resistant tuberculosis—a hope and a challenge. N Engl J Med. 2008;359:636–8.
- Borrell S, Gagneux S. Infectiousness, reproductive fitness and evolution of drug-resistant Mycobacterium tuberculosis. Int J Tuberc Lung Dis. 2009;13:1456–66.
- Ministry of Health. Labour and Welfare. Statistics of tuberculosis 2008 [in Japanese]. Tokyo: Japan Anti-Tuberculosis Association; 2009.
- Tuberculosis Research Committee (Ryoken). Drug-resistant Mycobacterium tuberculosis in Japan: a nationwide survey, 2002. Int J Tuberc Lung Dis. 2007;11:1129–35.
- Ministry of Health. Labour and Welfare. National guidelines for the epidemiological research [in Japanese]. 2002 [cited 2009 Nov 20]. http://www.mhlw.go.jp/shingi/2002/12/s1211-9e.html
- van Embden JD, Cave MD, Crawford JT, Dale JW, Eisenach KD, Gicquel B, Strain identification of Mycobacterium tuberculosis by DNA fingerprinting: recommendations for a standardized methodology. J Clin Microbiol. 1993;31:406–9.
- Kamerbeek J, Schouls L, Kolk A, van Agterveld M, van Soolingen D, Kuijper S, Simultaneous detection and strain differentiation of Mycobacterium tuberculosis for diagnosis and epidemiology. J Clin Microbiol. 1997;35:907–14.
- Brudey K, Driscoll JR, Rigouts L, Prodinger WM, Gori A, Al-Hajoj SA, Mycobacterium tuberculosis complex genetic diversity: mining the fourth international spoligotyping database (SpolDB4) for classification, population genetics and epidemiology. BMC Microbiol. 2006;6:23.
- Murase Y, Mitarai S, Sugawara I, Kato S, Maeda S. Promising loci of variable numbers of tandem repeats for typing Beijing family Mycobacterium tuberculosis. J Med Microbiol. 2008;57:873–80.
- Supply P, Allix C, Lesjean S, Cardoso-Oelemann M, Rusch-Gerdes S, Willery E, Proposal for standardization of optimized mycobacterial interspersed repetitive unit–variable-number tandem repeat typing of Mycobacterium tuberculosis. J Clin Microbiol. 2006;44:4498–510.
- European Concerted Action on New Generation Genetic Markers and Techniques for the Epidemiology and Control of Tuberculosis. Beijing/W genotype Mycobacterium tuberculosis and drug resistance. Emerg Infect Dis. 2006;12:736–43.
- Alonso-Rodriguez N, Martinez-Lirola M, Sanchez ML, Herranz M, Penafiel T, Bonillo Mdel C, Prospective universal application of mycobacterial interspersed repetitive-unit–variable-number tandem-repeat genotyping to characterize Mycobacterium tuberculosis isolates for fast identification of clustered and orphan cases. J Clin Microbiol. 2009;47:2026–32.
- Oelemann MC, Diel R, Vatin V, Haas W, Rusch-Gerdes S, Locht C, Assessment of an optimized mycobacterial interspersed repetitive-unit–variable-number tandem-repeat typing system combined with spoligotyping for population-based molecular epidemiology studies of tuberculosis. J Clin Microbiol. 2007;45:691–7.
- van Deutekom H, Supply P, de Haas PE, Willery E, Hoijng SP, Locht C, Molecular typing of Mycobacterium tuberculosis by mycobacterial interspersed repetitive unit–variable-number tandem repeat analysis, a more accurate method for identifying epidemiological links between patients with tuberculosis. J Clin Microbiol. 2005;43:4473–9.
- Godfrey-Faussett P, Stoker NG. Aspects of tuberculosis in Africa. 3. Genetic ‘fingerprinting’ for clues to the pathogenesis of tuberculosis. Trans R Soc Trop Med Hyg. 1992;86:472–5.
- Braden CR, Templeton GL, Cave MD, Valway S, Onorato IM, Castro KG, Interpretation of restriction fragment length polymorphism analysis of Mycobacterium tuberculosis isolates from a state with a large rural population. J Infect Dis. 1997;175:1446–52.
- Savine E, Warren RM, van der Spuy GD, Beyers N, van Helden PD, Locht C, Stability of variable-number tandem repeats of mycobacterial interspersed repetitive units from 12 loci in serial isolates of Mycobacterium tuberculosis. J Clin Microbiol. 2002;40:4561–6.
- Ano H, Matsumoto T, Suetake T, Nagai T, Tamura Y, Takamatsu I, Relationship between the isoniazid-resistant mutation katGS315T and the prevalence of MDR-/XDR-TB in Osaka, Japan. Int J Tuberc Lung Dis. 2008;12:1300–5.
- Tsuyuguchi K. Exogenous re-infection in tuberculosis [in Japanese]. Kekkaku. 2006;81:80–1.
- Kazumi Y, Itagaki N, Ohmori M, Wada M, Hoshino H, Mitarai S, Frequency of MDR-TB/XDR-TB strains isolated from chronic pulmonary tuberculosis patients in Japan [in Japanese]. Kekkaku. 2007;82:891–6.
- Andrews JR, Gandhi NR, Moodley P, Shah NS, Bohlken L, Moll AP, Exogenous reinfection as a cause of multidrug-resistant and extensively drug-resistant tuberculosis in rural South Africa. J Infect Dis. 2008;198:1582–9.
- Masjedi MR, Farnia P, Sorooch S, Pooramiri MV, Mansoori SD, Zarifi AZ, Extensively drug-resistant tuberculosis: 2 years of surveillance in Iran. Clin Infect Dis. 2006;43:841–7.
- Dahle UR. Extensively drug resistant tuberculosis: beware patients lost to follow-up. BMJ. 2006;333:705.
- Glynn JR, Bauer J, de Boer AS, Borgdorff MW, Fine PE, Godfrey-Faussett P, Interpreting DNA fingerprint clusters of Mycobacterium tuberculosis. European Concerted Action on Molecular Epidemiology and Control of Tuberculosis. Int J Tuberc Lung Dis. 1999;3:1055–60.
- Houben RM, Glynn JR. A systematic review and meta-analysis of molecular epidemiological studies of tuberculosis: development of a new tool to aid interpretation. Trop Med Int Health. 2009;14:892–909.
- Velayati AA, Masjedi MR, Farnia P, Tabarsi P, Ghanavi J, Ziazarifi AH, Emergence of new forms of totally drug-resistant tuberculosis bacilli: super extensively drug-resistant tuberculosis or totally drug-resistant strains in iran. Chest. 2009;136:420–5.
Suggested citation for this article: Murase Y, Maeda S, Yamada H, Ohkado A, Chikamatsu K, Mizuno K, et al. Clonal expansion of multidrug-resistant and extensively drug-resistant tuberculosis, Japan. Emerg Infect Dis [serial on the Internet]. 2010 Jun [date cited]. http://wwwnc.cdc.gov/eid/article/16/6/09-1844
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