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Consumer Sciences, Hyogo, Japan (M. Enomoto); Hiroshima City Institute of Public Health, Hiroshima, Japan (K. Abe, Y. Fujii, H. Tanaka, M. Yamamoto); and Kobayashi Pediatric Clinic, Shizuoka, Japan (M. Kobayashi) DOI: http://dx.doi.org/10.3201/eid1802.111147
References 1.
2.
3.
4.
5.
6.
7.
8.
9.
Infectious Disease Surveillance Center. Virus isolation/detection from hand, foot and mouth disease cases, 2007–2011. Infectious Agents Surveillance Report [cited 2011 Nov 7]. http://idsc.nih.go.jp/ iasr/prompt/s2graph-pke.html Infectious Disease Surveillance Center. Infectious Disease Weekly Report, Hand-foot-mouth disease cases reported per sentinel weekly [cited 2011 Nov 7]. http://idsc.nih.go.jp/idwr/kanja/weekly graph/06HFMD-e.html Perera D, Shimizu H, Yoshida H, Tu PV, Ishiko H, McMinn PC, et al. A comparison of the VP1, VP2, and VP4 regions for molecular typing of human enteroviruses. J Med Virol. 2010;82:649–57. Konno M, Yoshioka M, Sugie M, Maguchi T, Nakamura T, Kizawa M, et al. Fourteen years’ surveillance of coxsackievirus group A in Kyoto 1996‒2009 using mouse, RD-18S, and Vero cells. Jpn J Infect Dis. 2011;64:167–8. Wu Y, Yeo A, Phoon MC, Tan EL, Poh CL, Quak SH, et al. The largest outbreak of hand; foot and mouth disease in Singapore in 2008: the role of enterovirus 71 and coxsackievirus A strains. Int J Infect Dis. 2010;14:e1076–81. Österback R, Vuorinen T, Linna M, Susi P, Hyypia T. Waris M. Coxsackievirus A6 and hand, foot, and mouth disease, Finland. Emerg Infect Dis. 2009;15:1485– 8. Lo SH, Huang YC, Huang CG, Tsao KC, Li WC, Hsieh YC, et al. Clinical and epidemiologic features of coxsackievirus A6 infection in children in northern Taiwan between 2004 and 2009. J Microbiol Immunol Infect. 2011;44: 252–7. Blomqvist S, Klemola P, Kaijalainen S, Paananen A, Simonen ML, Vuorinen T, et al. Co-circulation of coxsackieviruses A6 and A10 in hand, foot and mouth disease outbreak in Finland. J Clin Virol. 2010;48:49–54. Guimbao J, Rodrigo P, Alberto MJ, Omenaca M. Onychomadesis outbreak linked to hand, foot, and mouth disease, Spain, July 2008. Euro Surveill. 2010;15:19663.
10.
Watanabe Y, Nanba C, Tohyama M, Machino H, Hashimoto K. Outbreak of nail matrix arrest following hand-footmouth disease [in Japanese]. Japanese Journal of Dermatology. 2011;121:863–7.
Address for correspondence: Hiroyuki Shimizu, Department of Virology II, National Institute of Infectious Diseases, Gakuen 4-7-1, Musashimurayama-shi, Tokyo 208-0011, Japan; email:
[email protected]
Human and Porcine Hepatitis E Viruses, Southeastern Bolivia To the Editor: Hepatitis E virus (HEV) genotypes 3 and 4 are considered to be primarily zoonotic (1). However, recent data indicate that both genotypes can be transmitted among humans through other routes (2,3). Observations of genetic distinctiveness between swine and human HEV strains circulating within the same region argue against exclusivity of zoonotic transmission (4). A recent report presented a remarkable example of such distinction between genotype 3 isolates in rural communities in southeastern Bolivia (5). We examined HEV sequences obtained in that study to show the independent genetic origin of swine and human variants. Findings suggest disjunction between human and swine HEV strains in this epidemiologic setting, despite the potential for extensive cross-species exposure. Using reference sequences from Lu et al. (6), we conducted subtype analysis of HEV open reading frame 2 sequences at nucleotide positions 826–1173 (GenBank accession no. AF060668) from isolates from 2 rural communities in southeastern Bolivia
(5). Analysis showed that swine sequences belonged to subtype 3i and that the human sequences belonged to 3e. We collected all available GenBank genotype 3 sequences covering this genomic region for which the dates of collection were documented. Sequences were used to estimate the time from the most recent common ancestor (tMRCA) by using BEAST version 1.6.1 (7). Estimated tMRCA for GenBank sequences was longer than for sequences from Bolivia alone (Table) or for all genotype 3 sequences together (Table). To reduce the effect of close relatedness among human or swine HEV sequences from Bolivia on the tMRCA estimate, we used only 1 representative sequence per species from each community in the final analysis. This analysis identified an estimated tMRCA similar to that seen for GenBank sequences alone (Table, model F vs. model D). This estimate indicates that human and swine HEV isolates from southeastern Bolivia last shared a common ancestor ≈275 years ago (Table, model F). Thus, swine HEV strains from both rural communities belonged to subtype 3i, and the human HEV strains identified from the community of Bartolo, Bolivia, belonged to subtype 3e and shared an ancestor with swine strains almost 3 centuries ago. This finding is surprising because the community of Bartolo has several potential risk factors for zoonotic transmission of HEV. There are ≈200 humans and ≈70 swine in Bartolo (8). Residents are mainly native Quechua and Guarani with some of mixed Spanish ancestry who subsist at a low socioeconomic level. Their main livelihood activities are agriculture and breeding of animals. Freerange pig farms are family owned. Because of its impoverished state, the community has no running water, and few houses have toilets. No facilities are suitable for safely slaughtering
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Table. Model estimates of time to most common recent ancestor for HEV ORF2 nucleotide sequences, southeastern Bolivia* 95% HPD, y Start Stop Bolivia GenBank Mean Mean ± SD rate of Lower Upper Model position position sequence sequence tMRCA, y substitutions/site/y –3 –6 A 826 1173 X NU 55.31 16.26 108.05 3.27 × 10 ± 9.44 × 10 –2 –4 B 826 1173 NU 3i and 3e 148.63 3.01 291.46 1.88 × 10 ± 6.41 × 10 –3 –5 C 826 1173 X X 144.45 38.66 298.20 3.43 × 10 ± 4.74 × 10 –3 –5 D 826 1173 NU X 328.05 45.59 681.90 2.12 × 10 ± 7.33 × 10 –4 –5 E 1 1980 NU X 296.06 163.40 467.97 9.27 × 10 ± 1.25 × 10 –3 –5 F 826 1173 3 seqs X 275.45 40.06 635.32 2.40 × 10 ± 5.06 × 10 *HEV, hepatitis E virus; ORF, open reading frame; tMRCA, time to the most recent common ancestor; HPD, highest posterior density boundary; X, sequences was used; NU, not used; 3i and 3e, subtype 3i and 3e sequences were used; 3 seqs, sequences (CV2, CB9, and HB2BA053) from Bolivia were used.
animals (5,9). These conditions appear to create a setting in which zoonotic transmission of HEV should be common, and infection should be caused by a strain shared between swine and humans. However, the data suggest host-specific infection with distinct HEV subtypes. Although specimens were collected from 172 humans (≈86%) and 67 swine (≈96%) in Bartolo (8), zoonotically transmitted isolates may have been missed because of the sample-pooling technique used (5). Nevertheless, detection of distinct HEV strains in human and swine populations indicates possible nonzoonotic, human-to-human transmission in this community. Detection of antibodies against HEV among 7% of residents and HEV genomes in persons without serologic markers of HEV infection indicate a higher HEV prevalence in Bartolo (5). Subclinical infection detected by PCR among Bartolo residents (5), rapid decrease of HEV antibody, and uncertain sensitivity of commercial serologic assays (10) suggest that the reported extent of HEV infection is most likely an underestimate. High prevalence may generate conditions in this community that effectively prevent cross-species transmission because of frequent exposure to HEV early in life when contacts between humans and animals are limited, thus promoting host-specific transmission. This supposition is supported by the higher seropositivity seen among children 1–5 years of age and adults 41–50 years of
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age in Bartolo (5). Implications of these observations for understanding HEV evolution and epidemiology of HEV infections warrant further research on genetic heterogeneity of HEV strains in this region and other epidemiologic settings. Michael A. Purdy, Maria Chiara Dell’Amico, José Luis Gonzales, Higinio Segundo, Francesco Tolari, Maurizio Mazzei, Alessandro Bartoloni, and Yury E. Khudyakov Author affiliations: Centers for Disease Control and Prevention, Atlanta, Georgia USA (M. A. Purdy, Y. E. Khudyakov); Università di Pisa, Pisa, Italy (M. C. Dell’Amico, F. Tolari, M. Mazzei); Laboratorio de Investigación y Diagnóstico Veterinario, Santa Cruz, Bolivia (J. L. Gonzales); Distrito de Salud Cordillera, Santa Cruz, Bolivia (H. Segundo); and Università degli Studi di Firenze, Firenze, Italy (A. Bartoloni) DOI: http://dx.doi.org/10.3201/eid1802.111453
References 1.
2.
Meng XJ. From barnyard to food table: the omnipresence of hepatitis E virus and risk for zoonotic infection and food safety. Virus Res. 2011;161:23–30. http://dx.doi. org/10.1016/j.virusres.2011.01.016 Matsubayashi K, Kang JH, Sakata H, Takahashi K, Shindo M, Kato M, et al. A case of transfusion-transmitted hepatitis E caused by blood from a donor infected with hepatitis E virus via zoonotic foodborne route. Transfusion. 2008;48:1368– 75. http://dx.doi.org/10.1111/j.15372995.2008.01722.x
3.
Purdy MA, Khudyakov YE. Molecular epidemiology of hepatitis E virus infection. Virus Res. 2011;161:31–9. http:// dx.doi.org/10.1016/j.virusres.2011.04.030 4. Zhu Y-M, Dong S-J, Si F-S, Yu RS, Li Z, Yu XM, et al. Swine and human hepatitis E virus (HEV) infection in China. J Clin Virol. 2011;52:155–7. http://dx.doi. org/10.1016/j.jcv.2011.06.023 5. Dell’Amico MC, Cavallo A, Gonzales JL, Bonelli SI, Valda Y, Pieri A, et al. Hepatitis E virus genotype 3 in humans and swine, Bolivia. Emerg Infect Dis. 2011;17:1488– 90. 6. Lu L, Li C, Hagedorn CH. Phylogenetic analysis of global hepatitis E virus sequences: genetic diversity, subtypes and zoonosis. Rev Med Virol. 2006;16:5–36. http://dx.doi.org/10.1002/rmv.482 7. Purdy MA, Khudyakov YE. Evolutionary history and population dynamics of hepatitis E virus. PLoS ONE. 2010;5:e14376. h t t p : / / d x . d o i . o rg / 1 0 . 1 3 7 1 / j o u r n a l . pone.0014376 8. Dell’Amico MC. Infezione da virus dell’epatite e nel suino e nell’uomo: aggiornamento sulle metodiche diagnostiche di laboratorio. Bologna (Italy): Università di Bologna; 2009. 9. Bartoloni A, Bartalesi F, Roselli M, Mantella A, Arce CC, Paradisi F, et al. Prevalence of antibodies against hepatitis A and E viruses among rural populations of the Chaco region, south-eastern Bolivia. Trop Med Int Health. 1999;4:596– 601. http://dx.doi.org/10.1046/j.13653156.1999.00457.x 10. Khudyakov Y, Kamili S. Serological diagnostics of hepatitis E virus infection. Virus Res. 2011;161:84–92. http://dx.doi. org/10.1016/j.virusres.2011.06.006 Address for correspondence: Michael A. Purdy, Centers for Disease Control and Prevention, 1600 Clifton Rd NE, Mailstop A33, Atlanta, GA 30333, USA; email:
[email protected] All material published in Emerging Infectious Diseases is in the public domain and may be used and reprinted without special permission; proper citation, however, is required.
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