Acta Veterinaria Scandinavica | |
Repeated examination of natural sapovirus infections in pig litters raised under experimental conditions | |
Klara Tølbøll Lauritsen1  Mette Sif Hansen1  Christina K. Johnsen2  Gregers Jungersen1  Blenda Böttiger3  | |
[1] National Veterinary Institute, Technical University of Denmark, Bülowsvej 27, Frederiksberg C, 1870, Denmark | |
[2] TransMedEdit, Syvendehusvej 52, Ballerup, 2750, Denmark | |
[3] Department of Laboratory Medicine, Medical Microbiology, Lund University, Sölvegatan 23, Lund, 22185, Sweden | |
关键词: Phylogenetic analysis; RT-PCR; Swine; Caliciviridae; Sapovirus; | |
Others : 1227520 DOI : 10.1186/s13028-015-0146-7 |
|
received in 2015-03-29, accepted in 2015-09-02, 发布年份 2015 |
【 摘 要 】
Background
Porcine sapovirus, belonging to the family Caliciviridae, is an enteric virus that is widespread in the swine industry worldwide. A total of 14 sapovirus genogroups have been suggested and the most commonly found genogroup in swine is genogroup III (GIII). The goal of the present experiment was to examine the presence of sapovirus in 51 naturally infected pigs at two different time points. The pigs were kept under experimental conditions after weaning. Previous studies on sapovirus have primarily been of a cross sectional nature, typically prevalence studies performed on farms and abattoirs. In the present study, faecal samples, collected from each pig at 5½ weeks and 15–18 weeks of age, were analysed for sapovirus by reverse transciptase polymerase chain reaction and positive findings were genotyped by sequencing.
Results
At 5½ weeks of age, sapovirus was detected in the majority of the pigs. Sequencing revealed four different strains in the 5½ week olds—belonging to genogroups GIII and GVII. Ten to 13 weeks later, the virus was no longer detectable from stools of infected pigs. However, at this time point 13 pigs were infected with another GIII sapovirus strain not previously detected in the pigs studied. This GIII strain was only found in pigs that, in the initial samples, were virus-negative or positive for GVII.
Conclusions
At 5 weeks of age 74 % of the pigs were infected with sapovirus. At 15–18 weeks of age all pigs had cleared their initial infection, but a new sapovirus GIII strain was detected in 25 % of the pigs. None of the pigs initially infected with the first GIII strain were reinfected with this new GIII strain, which may indicate the presence of a genogroup-specific immunity.
【 授权许可】
2015 Lauritsen et al.
Files | Size | Format | View |
---|---|---|---|
Fig.1. | 20KB | Image | ![]() |
Fig.1. | 20KB | Image | ![]() |
【 图 表 】
Fig.1.
Fig.1.
【 参考文献 】
- [1]Schlenker C, Surawicz CM. Emerging infections of the gastrointestinal tract. Best Pract Res Clin Gastroenterol. 2009; 23:89-99.
- [2]Flynn WT, Saif LJ, Moorhead PD. Pathogenesis of porcine enteric calicivirus-like virus in four-day-old gnotobiotic pigs. Am J Vet Res. 1988; 49:819-825.
- [3]Guo M, Hayes J, Cho KO, Parwani AV, Lucas LM, Saif LJ. Comparative pathogenesis of tissue culture-adapted and wild-type Cowden porcine enteric calicivirus (PEC) in gnotobiotic pigs and induction of diarrhea by intravenous inoculation of wild-type PEC. J Virol. 2001; 75:9239-9251.
- [4]Collins PJ, Martella V, Buonavoglia C, O’Shea H. Detection and characterization of porcine sapoviruses from asymptomatic animals in Irish farms. Vet Microbiol. 2009; 139:176-182.
- [5]Keum HO, Moon HJ, Park SJ, Kim HK, Rho SM, Park BK. Porcine noroviruses and sapoviruses on Korean swine farms. Arch Virol. 2009; 154:1765-1774.
- [6]Mauroy A, Scipioni A, Mathijs E, Miry C, Ziant D, Thys C, Thiry E. Noroviruses and sapoviruses in pigs in Belgium. Arch Virol. 2008; 153:1927-1931.
- [7]Reuter G, Zimsek-Mijovski J, Poljsak-Prijatelj M, Di Bartolo I, Ruggeri FM, Kantala T et al.. Incidence, diversity and molecular epidemiology of sapoviruses in swine across Europe. J Clin Microbiol. 2010; 48:363-368.
- [8]Zhang W, Shen Q, Hua X, Cui L, Liu J, Yang S. The first Chinese porcine sapovirus strain that contributed to an outbreak of gastroenteritis in piglets. J Virol. 2008; 82:8239-8240.
- [9]Cunha JB, de Mendonça MC, Miagostovich MP, Leite JP. Genetic diversity of porcine enteric caliciviruses in pigs raised in Rio de Janeiro State, Brazil. Arch Virol. 2010; 155:1301-1305.
- [10]Liu GH, Li RC, Huang ZB, Yang J, Xiao CT, Li J et al.. RT-PCR test for detecting porcine sapovirus in weanling piglets in Hunan Province, China. Trop Anim Health Prod. 2012; 44:1335-1339.
- [11]Martínez MA, Alcalá AC, Carruyo G, Botero L, Liprandi F, Ludert JE. Molecular detection of porcine enteric caliciviruses in Venezuelan farms. Vet Microbiol. 2006; 116:77-84.
- [12]Dufkova L, Scigalkova I, Moutelikova R, Malenovska H, Prodelalova J. Genetic diversity of porcine sapoviruses, kobuviruses, and astroviruses in asymptomatic pigs: an emerging new sapovirus GIII genotype. Arch Virol. 2013; 158:549-558.
- [13]Yu JN, Kim MY, Kim DG, Kim SE, Lee JB, Park SY et al.. Prevalence of hepatitis E virus and sapovirus in post-weaning pigs and identification of their genetic diversity. Arch Virol. 2008; 153:739-742.
- [14]Wang QH, Souza M, Funk JA, Zhang W, Saif LJ. Prevalence of noroviruses and sapoviruses in swine of various ages determined by reverse transcription-PCR and microwell hybridazation assays. J Clin Microbiol. 2006; 44:2057-2062.
- [15]Di Bartolo I, Tofani S, Angeloni G, Ponterio E, Ostanello F, Ruggeri FM. Detection and characterization of porcine caliciviruses in Italy. Arch Virol. 2014; 159:2479-2484.
- [16]Bank-Wolf BR, König M, Thiel HJ. Zoonotic aspects of infections with noroviruses and sapoviruses. Vet Microbiol. 2010; 140:204-212.
- [17]Wang QH, Han MG, Funk JA, Bowman G, Janies DA, Saif LJ. Genetic diversity and recombination of porcine sapoviruses. J Clin Microbiol. 2005; 43:5963-5972.
- [18]L’Homme Y, Sansregret R, Plante-Fortier E, Lamontagne AM, Lacroix G, Ouardani M et al.. Genetic diversity of porcine Norovirus and Sapovirus: Canada, 2005–2007. Arch Virol. 2009; 154:581-593.
- [19]Song YJ, Yu JN, Nam HM, Bak HR, Lee JB, Park SY et al.. Identification of genetic diversity of porcine Norovirus and Sapovirus in Korea. Virus Genes. 2011; 42:394-401.
- [20]Scheuer KA, Oka T, Hoet AE, Gebreyes WA, Molla BZ, Saif LJ, Wang Q. Prevalence of porcine noroviruses, molecular characterization of emerging porcine sapoviruses from finisher swine in the United States, and unified classification scheme for sapoviruses. J Clin Microbiol. 2013; 51:2344-2353.
- [21]Martella V, Lorusso E, Banyai K, Decaro N, Corrente M, Elia G et al.. Identification of a porcine calicivirus related genetically to human sapoviruses. J Clin Microbiol. 2008; 46:1907-1913.
- [22]Jiang X, Huang PW, Zhong WM, Farkas T, Cubitt DW, Matson DO. Design and evaluation of a primer pair that detects both Norwalk- and Sapporo-like caliciviruses by RT-PCR. J Virol Methods. 1999; 83:145-154.
- [23]Farkas T, Zhong WM, Jing Y, Huang PW, Espinosa SM, Martinez N et al.. Genetic diversity among sapoviruses. Arch Virol. 2004; 149:1309-1323.
- [24]Wang QH, Costantini V, Saif LJ. Porcine enteric caliciviruses: genetic and antigenic relatedness to human caliciviruses, diagnosis and epidemiology. Vaccine. 2007; 25:5453-5466.
- [25]Barry AF, Alfieri AF, Alfieri AA. High genetic diversity in RdRp gene of Brazilian porcine sapovirus strains. Vet Microbiol. 2008; 131:185-191.
- [26]Shen Q, Zhang W, Yang S, Chen Y, Ning H, Shan T et al.. Molecular detection and prevalence of porcine caliciviruses in eastern China from 2008 to 2009. Arch Virol. 2009; 154:1625-1630.
- [27]Johnson PC, Mathewson JJ, DuPont HL, Greenberg HB. Multiple-challenge study of host susceptibility to Norwalk gastroenteritis in US adults. J Infect Dis. 1990; 161:18-21.
- [28]Bull RA, White PA. Mechanisms of GII.4 norovirus evolution. Trends Microbiol. 2011; 19:233-240.