| Literature DB >> 24520348 |
Huanbin Liang1, Shuo Su1, Shengchao Deng1, Honglang Gu1, Fangxiao Ji1, Lifang Wang1, Chumin Liang1, Heng Wang1, Guihong Zhang1.
Abstract
Hepatitis E virus (HEV) infection is widespread in China, but few studies have been carried out in Guangdong Province. This study aimed to characterize the prevalence of HEV infections among swine, swine farmers and the general population in Guangdong Province. We conducted an epidemiological study that included swine, swine farmers and health examination attendees in Guangdong from 2011 to 2013. The overall seroprevalence of anti-HEV antibodies in swine was 64.7%. The results revealed that growing pigs, sows and boars (OR ranges from 3.5 to 21.5) have a higher risk than nursery pigs. HEV RNA in swine bile showed that HEV is epidemic in swine in the Pearl River Delta, with the highest prevalence of 22.73% in Foshan. Some genomes of HEV strains from each district were sequenced. Phylogenetic analysis of partial open reading frame 2 (ORF2) shows that they belong to genotype IV and are most closely related to isolates from China. In total, 307 participants were enrolled in the study, including 114 swine farmers and 193 attendees from hospitals. IgG anti-HEV was detected in 48.25% of swine farmers and in 38.34% of the general population. Seroprevalence rates were almost stratified by age, with a higher positive rate for males compared to females across all age groups. Women on swine farms appeared to have a lower risk of infection compared to the general population, revealing that the risk factors for HEV infection are not unique. The results suggested that there were other risk factors for HEV infection. HEV infection is prevalent in Guangdong, but due to the small sample sizes, more investigations are needed to assess the potential impact of HEV infection, and many additional risk factors should be considered.Entities:
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Year: 2014 PMID: 24520348 PMCID: PMC3919735 DOI: 10.1371/journal.pone.0088106
Source DB: PubMed Journal: PLoS One ISSN: 1932-6203 Impact factor: 3.240
The information of swine farms and samples.
| Farm | Bile(positive/total) | Farm | Serum(positive/total) | ||||||
| N | G | S | B | N | G | S | B | ||
| Dongguan1 | 1/5 | 0/7 | 0/1 | 1/1 | A | 4/12 | 0 | 26/30 | 6/7 |
| Dongguan2 | 0 | 1/6 | 1/1 | 0/1 | B | 6/13 | 0 | 25/33 | 7/7 |
| Foshan1 | 0/3 | 1/5 | 1/1 | 1/1 | C | 1/7 | 0 | 18/28 | 6/6 |
| Foshan2 | 2/8 | 1/6 | 1/2 | 0 | D | 4/14 | 5/12 | 14/20 | 2/3 |
| Foshan3 | 1/7 | 2/10 | 0/1 | 0 | E | 6/12 | 3/6 | 16/18 | 3/4 |
| Guangzhou1 | 0/2 | 1/9 | 0/1 | 0 | F | 2/12 | 8/18 | 11/20 | 4/4 |
| Guangzhou2 | 0 | 1/7 | 0/1 | 0 | G | 3/8 | 9/11 | 17/24 | 5/5 |
| Huizhou1 | 0/2 | 2/11 | 0/2 | 0 | H | 3/9 | 7/10 | 16/22 | 5/5 |
| Huizhou2 | 1/5 | 1/7 | 0 | 0 | I | 5/16 | 7/8 | 19/25 | 6/6 |
| Huizhou3 | 0 | 2/13 | 0 | 0 | J | 3/9 | 5/5 | 19/19 | 5/5 |
| Jiangmen1 | 0/3 | 1/10 | 1/1 | 1/1 | K | 4/11 | 4/4 | 16/22 | 4/5 |
| Jiangmen2 | 1/9 | 2/12 | 1/2 | 0 | L | 5/10 | 4/6 | 11/25 | 4/5 |
| Jiangmen3 | 1/3 | 0/5 | 2/2 | 0 | |||||
| Shenzhen1 | 0/2 | 0/4 | 0/1 | 0 | |||||
| Shenzhen2 | 0/2 | 1/6 | 1/1 | 0 | |||||
| Zhaoqing1 | 0/6 | 1/8 | 0 | 0 | |||||
| Zhaoqing2 | 0/7 | 1/10 | 0/1 | 0 | |||||
| Zhongshan1 | 2/6 | 1/7 | 0/1 | 0 | |||||
| Zhongshan2 | 1/4 | 1/5 | 0/1 | 0 | |||||
| Zhongshan3 | 1/6 | 2/9 | 0/1 | 0 | |||||
| Zhuhai1 | 1/6 | 0/8 | 1/2 | 0 | |||||
| Zhuhai2 | 1/4 | 1/4 | 0/2 | 0 | |||||
| Total | 13/90 | 23/169 | 9/25 | 3/4 | 46/133 | 52/80 | 208/286 | 57/62 | |
Bile samples were collected from 22 different swine farms including large-scale farms and family-scale farms in 9 districts of Pearl River Delta. Swine sera were sampled from 12 large-scale swine farm in Guangdong. N, nursery pig; G, growing pig; S, sow; B, boar.
Figure 1A phylogenetic tree based on the full nucleotide sequence of HEV.
Total RNA positive bile samples are 48, from 9 different districts in Guangdong. We have chosen at least one sample from each district by random sampling. The amplification products of ORF2 (509 nucleotides, primer sequences were HEV-INF and HEV-INR as described above) from 10 positive bile samples were sequenced and compared. The nucleotide sequence identity among the 10 swine HEV isolates obtained from pigs from different farms in three years ranged between 94.3 and 99.8%. Phylogenetic trees were constructed by the neighbor-joining method based on the partial nucleotide sequence of the ORF2 region (509 nucleotides). The bootstrap values (expressed as percentages) were determined on 1000 re-samplings of the data sets. △were the isolates in this study.
The prevalence of antibodies against HEV among pigs in 2011–2013, Guangdong Province, China.
| Serum sample | Univariate analysis | ||||
| Positive/Total (n) | Positive rate (%) | ORa (95% CI b) | X2 c | P value | |
| Different swine farm | |||||
| Nursery pig (<4 wks) | 46/133 | 34.59 | refd | ||
| Growing pig (>4 wk-6 mos) | 52/80 | 65.00 | 3.51(1.95–6.33) | 17.40 | <104 |
| Sow (>7 mos) | 208/286 | 72.72 | 5.04(3.27–7.77) | 53.74 | <104 |
| Boar (>7 mos) | 57/62 | 91.93 | 21.56(9.47–49.10) | 53.53 | <104 |
| Sow | |||||
| Pre-farrowing sow | 58/96 | 60.42 | ref | ||
| Multiparous sow | 150/190 | 78.95 | 2.46(1.45–4.18) | 10.13 | <0.01 |
a: OR, odds ratio;
b: 95%CI, 95%confidence interval;
c: X2, Chi-Square Test;
d: ref, reference.
Figure 2Fourfold plot for odds ratio (OR).
Univariate analysis results are presented in the Fourfold plot diagram. Fourfold display for seropositive data of sows: Evidence for pig herds bias or multiparity bias? The area of eachshaded quadrant shows the frequency, standardized to equate the margins for different herds and seropositive. Circular arcs show the limits of a 95% confidence interval for the odds ratio. 1. Compared with nursery pigs, the OR of growing pigs was 3.51(95%CI, 1.95–6.33; p<0.0001); 2. Compared with nursery pigs, the OR of sows was 5.04(95%CI, 3.27–7.77; p<0.0001); 3. Compared with nursery pigs, the OR of boars was 21.56(95%CI, 9.47–49.10; p<0.0001); 4. Compared with pre-farrowing sows, the OR of multiparous sows was 2.46(95%CI, 1.45–4.18; p<0.01).
The prevalence of HEV RNA in pig bile samples collected from the Pearl River Delta. b
| District | No. of bile samples | No. of positive HEV RNA samples | Analysis | |
| positive rate (%) | 95% CI | |||
| Dongguan | 22 | 4 | 18.18 | 2.5–33.86 |
| Foshan | 44 | 10 | 22.73 | 10.35–35.11 |
| Guangzhou | 20 | 2 | 10.00 | 0–23.14 |
| Huizhou | 40 | 6 | 15.00 | 3.93–26.07 |
| Jiangmen | 48 | 10 | 20.83 | 9.34–32.32 |
| Shenzhen | 16 | 2 | 12.50 | 0–28.70 |
| Zhaoqing | 32 | 2 | 6.25 | 0–14.64 |
| Zhongshan | 40 | 8 | 20.00 | 8.24–31.76 |
| Zhuhai | 26 | 4 | 15.38 | 1.51–29.25 |
Pig bile samples have been collected from 9 districts of the Pearl River Delta since 2011.
Figure 3A map indicating the prevalence of HEV RNA in the Pearl River Delta of Guangdong Province.
The anti-HEV rates of the population in Guangdong province, China, according to age, gender, and pig-exposure status.
| Sample | Univariate analysis | |||||
| Positive/Total (n) | Positive rate (%) | ORa (95% CIb) | X2 c | P value | ||
| Age | ||||||
| ≤29 | 22/88 | 25.00 | refd | |||
| 30–39 | 24/76 | 31.58 | 1.38(0.60–3.21) | 0.58 | 0.45 | |
| 40–49 | 51/88 | 57.95 | 4.14(2.15–7.96) | 18.35 | <104 | ** |
| 50–59 | 14/29 | 48.28 | 2.80(1.09–7.22) | 4.51 | <0.05 | * |
| ≥60 | 18/26 | 69.23 | 6.75(2.60–17.54) | 15.35 | <104 | ** |
| Gender | ||||||
| UF | 30/77 | 38.96 | ref | |||
| UM | 44/116 | 37.93 | 0.96(0.60–1.54) | 0.03 | ≈1 | |
| FF | 19/47 | 40.43 | ref | |||
| FM | 36/67 | 53.73 | 1.71(0.72–4.08) | 1.46 | 0.23 | |
| Pig-exposure | ||||||
| UF | 30/77 | 38.96 | ref | |||
| FF | 19/47 | 40.43 | 1.06(0.54–2.08) | 0.03 | ≈1 | |
| UM | 44/116 | 37.93 | ref | |||
| FM | 36/67 | 53.73 | 1.90(0.99–3.66) | 3.69 | 0.05 | |
a: OR, odds ratio; b: 95%CI, 95%confidence interval; c: X2, Chi-Square Test; d: ref, reference; UF, urban female; UM, urban male; FF, swine farm female; FM, swine farm male; **, significant difference; *, different.
Figure 4The estimated seroprevalence of the hepatitis E virus in Guangdong Province.
The best fit trendline for the positive rate data was selected based on the R-squared value of the curves drawn using the Microsoft Office Excel 2007 program (Microsoft, Redmond, WA). 1. Overall gender-specific seroprevalence; 2. Gender-specific seroprevalence of swine farm; 3. Gender-specific seroprevalence of the general population; 4. Overall population-specific seroprevalence; 5. Population-specific seroprevalence of females; 6. Population-specific seroprevalence of males.