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Epidemiology and immunoprotection of nephropathogenic avian infectious bronchitis virus in southern China
Virology Journalvolume 8, Article number: 484 (2011)
In last three years, 96 suspected poultry farms from different provinces in China were diagnosed for avian infectious bronchitis (IB) survey. Finally, 221 IBV strains were confirmed by dwarf embryo test and RT-PCR assay. By virus recovery trials, 187 of the isolates caused the birds died or distressed from nephritis, which was accordant with the clinical record.
Based on epidemiology analysis of recent field isolates of nephropathogenic IB in vaccinated farms in China, YL6 strain were used for vaccination and evaluated by antibody titer and challenge tests. The immunoprotection test indicated that the practical application of vaccine based on the recent field strains could finely facilitate controlling the nephropathogenic IB.
Our study was aim at setting a guide for safeguard against nephropathogenic IBV-caused disease in China.
Infectious bronchitis (IB) is a serious and highly contagious disease of chickens all over the world. Avian infectious bronchitis virus (IBV) was first reported in the USA for replicating in the respiratory tract and some other epithelial cells of gut, kidney, and oviduct. Subsequently, some strains of IBV caused pathology in non-respiratory organs (such as kidney and gonads) were documented . The clinical disease and production problems frequently cause catastrophic economic losses to the poultry industry, accompanied by decreased production performance in breeder flocks, diminished egg production and poor egg quality in laying flocks [1–3]. In China, IB has a more profound social impact for chicken industrial contributes to the rural economy. More importantly, there is accumulating evidence that nephropathogenic type IB has been more and more prevalent in China recently, but the strains isolated in earlier years mainly caused respiratory signs, which suggested that selecting and immunization with the appropriate vaccine strain is of great importance to control IB infection [4–7].
Some researchers reported that satisfactory cross protection could be provided by appropriate vaccine programs against genetically or antigenically unrelated IBVs . However, this symphysial vaccine manner was restricted by the diversity of the IBV strains. Since IBV strains were first isolated and identified in China in 1982, various live-attenuated and inactivated vaccines derived from respiratory-typed strains have been widely and extensively used in chicken farms to reduce the adverse effect of the IBV [6, 7]. However, the disease continues to emerge and cause serious production problems, even occurred in routinely vaccinated layer and breeder flocks in China, and the situation gets worse as time progressed . The most possible explanation for this phenomenon may be that the vaccine effectiveness is diminished by poor cross-protection against the circulating strains.
The spike tip glycoprotein (S1) of virus particle has direct relation to induce virus neutralizing antibody, and determines the cross-protection [10, 11]. Our previous research had confirmed that the predominant IBVs were nephropathogenic IBVs were mainly A2-like strains in China during 2008-2009 . This study was to further investigate the prevalence of nephropathogenic IB under immune pressure with routine vaccine strains in China. Additionally, the effectiveness of vaccination program using the common field strains practically against IB was also verified.
Isolated IBV strains during 2008 to 2010
From unhealthy birds suspected of IBV infection in the vaccinated chicken farms from Guangdong, Guangxi, Fujian, Hainan, Jiangsu, Zhejiang, Chongqing, Hubei, Sichuan and Jiangxi province of China, 221 filed IBV strains isolated during 2008-2010 were confirmed by RT-PCR, including 214 strains isolated from broilers, and 7 strains from broiler breeder. The isolation rates in the three years were season-dependent to some extent, 58 strains were isolated in early summer (April and May) and 99 strains were isolated in fall and winter (from September to January). The ages of flocks at the time of the outbreak varied between 4 and 70 days. Nearly half (110/221) of the isolated strains were isolated from the chickens between 10 to 30 days of age, seven strains below 10 days, and six strains above 60 days. Eighty of the 221 isolates have been molecular analyzized to be mainly A2-like strains .
Since the fourth day post-inoculation, most of the chicks were listless and huddled together, showed appetite and weight lose. The virus recovery tests indicated 84.6% (187/221) isolates caused serious kidney lesions, which were presented with swollen specked kidney and distended ureters filled with uric acid, and the other isolates caused respiratory system signs. All the above were consistent with the clinical record of each strain.
Vaccination test and challenge protection
After the birds were vaccinated, sera were collected and identified by ELISA, the antibody titer was kept ascending slowly, on 10 days after the second immunization reached to a considerable level, even better before challenge, but none in the control group 4 (unvaccinated but challenged).
As showed in Table 1, there wasn't obvious discrepancy in the antibody levels of Group 1, 2 and 3, inoculated with vaccine XZB and YL6, but much higher than the control Group 4. The chicks at 24 days old of Group 3 were a bit higher than Group 1 and 2. Since the second day post challenge with IBVs, all of the chickens in the four groups showed transitory and mild respiratory signs, including tracheal rales, sneezing and coughing. Postmortem examination of dead and sacrificed birds, revealed the renal petechial haemorrhages, urates deposition and degenerative changes in renal tubules. While in the chickens of group 3, there was no morbidity, and all of the clinical signs of these challenged birds tended to disappear gradually after two weeks of challenge test (Table 2). Finally, the birds were validated to be no virus detected by virus isolation through tracheal swabs after three weeks post challenge. The results of vaccine-challenge trials indicated that combined immunization with vaccine XZB and YL6 used in chickens could induce prevention against the infection of nephropathogenic IBV. The protection effect of XZB (vaccinated once or twice) was weaker.
After five-month practical application in the field, it was proved that using the YL6 inactivated vaccine could basically control the prevalence of nephropathogenic IB, inducing excellent protection (94%). The broilers and breeders would not be infected, and the satisfactory immunity would prevent the hens from lower fertilized rate, reduced egg quality and laying quantity, and the progeny chicken could get a high level of maternally antibodies.
Infectious bronchitis (IB) is one of the most common and difficult-control poultry diseases in China, caused persistent but infrequent outbreaks in commercial chicken farms [9, 12, 13]. The clinical cases caused by vaccination failure raised the importance to investigate the circulating nephropathogenic IBVs and select the candidate vaccine strain against the infections [1, 12].
In this study, 221 IBV strains were isolated from the vaccinated chicken flocks, with a wide age range of IB outbreak, 51.6% (117/221) of the birds were not older than 30 days. The chickens infected before the age of 10 days which might be resulted from the maternal antibody could not provide pertinent protection against the prevalent strains. Nowadays, various nephropathogenic strains of IBV have been identified throughout the world. The prevalence of nephropathogenic IB becomes to be a problem for chicken industry in China in recent few years [4, 5, 7]. Through clinical records and the virus recovery trials, 187 identified isolates mainly caused typical swollen kidney, different from the respiratory type strains isolated in earlier years, including the major vaccine strains.
The vaccine-challenge tests further demonstrated that chicks vaccinated with currently used vaccines in China cannot provide sufficient protection against the prevalent virus strain. The antibody titers evaluated by ELISA were closely associated with the antigen differences. The complex antigen variations of IB caused the antibody titers were just referenced, which showed no obvious discrepancy between commercial and field vaccine in this study. The effective of vaccines were dependent on the protection rate. Absorbingly, the commercial vaccine associated with the inactivated oil-emulsion vaccine (novel field strains) can satisfactorily prevent the vaccinated birds against the infections. The inactivated oil-emulsion vaccine (YL6) associated with commercial vaccines have been used in some flocks, and effectively controlled the supposed IB outburst from 2009 to 2010.
The S1 protein determined the serotypic evolution, the phenotype change and the genetic diversity of IBVs [11, 14]. The commercial vaccine was consisted of H120 strain and W93 strain, the latter one was nephropathogenic strain, but attenuated and started for vaccination in 1990s. The error-prone nature of RNA polymerase made the S1 gene could easily generate mutations to bring about new variation strain. Persistent evolutionary variations caused the distant genetic relationship between the vaccine strains and the circulating strains. Our previous report had determined that nephropathogenic IBVs were mainly A2-like strains in China in recent years, showed evolutionarily distant from vaccine strains .
In conclusion, the data obtained from our study suggested the satisfactory immunoprotection of the YL6 vaccine, which genetically belonged to the A2-type group, used in the southern China. To control the prevalence and well prepare for the potential outbreaks of IB, the candidate virus strain for vaccination might be selected timely. Therefore, continuing surveillance of new IBV strains and selecting the representative virus strain for vaccination would be the most effective manner to reduce the economic losses caused by IB. We hope the study could contribute to guiding the development of effective vaccines and establishment of control policy for nephropathogenic IB.
Materials and methods
Virus isolation and identification
During the period from June 2008 to November 2010, IBV surveys were performed in 96 suspected but vaccinated flocks from eastern, southern, southwestern and central China. Documented clinical signs of the birds included respiratory and typical nephropathogenic symptoms. Viruses in the homogenized tissue pool of kidney and trachea of the field isolates were propagated by inoculating via the allantoic cavity of 10 day old SPF embryonated eggs for more than three passages. The embryos dying within 24 hours of inoculation were screened to be nonspecific deaths. The isolates caused stunting, dwarfing, curling of the embryo or the presence of urates in the mesonephros after 5 days incubation were indicative of IB virus replication. The viruses were further confirmed by RT-PCR assays. The allantoic fluids containing IBV isolates after 72 h post inoculation were harvested and preserved in liquid nitrogen.
Total RNA extraction of the allantoic fluid was completed using RNAiso reagent (TaKaRa Biotechnology, Dalian, China) according to the manufacturers' instructions. Reverse transcription polymerase chain reaction (RT-PCR) was carried out by PrimeScriptTM One-Step RT-PCR Kit in 25 μl reaction volume containing 20 μl of RT-PCR PreMix (reaction buffer, dNTPs, 2 μl of enzyme mix), 2 μl of extracted viral RNA and the specific primers (National standard, GBT23197-2008), one primer pair targeting the M gene (Ms: 5'-CCTAAGAACGGTTGGAAT-3', Mx: 5'-TACTCTCTACAC ACACAC-3') and another pair for the 3' UTR of genome (3's: 5'-GGAAGATAGGCATGTAGCTT-3', 3'x: 5'-CTAACTCTATACTAGCCTAT-3').
After IBV confirmation, virus recovery was performed as previous described . Five 1-day-old SPF White Leghorn chickens were intranasally inoculated with each isolate, respectively. All of the chicks were examined and recorded daily for clinical signs for 20 days post inoculation, the dead birds were necrospied for lesions of respiratory tract or nephritis. Finally, all the survivors were sacrificed and necrospied. All of the animal experiments were conducted in accordance with the guidelines of Guangdong Province on the Review of Welfare and Ethics of Laboratory Animals, and under the protocol (SCAU-AEC-2010-1102) approved by the Animal Ethics Committee of South China Agricultural University.
Vaccination-challenge of immunity trials and clinical application
Based on clinical records and sequence blast from our previous report, YL6 strain (GenBank accession numbers: GU938393 for S1 gene) isolated from Yulin city of Guangxi province in June 2009 (with high morbidity of 100% and mortality of 79%) was selected for preparation of inactivated oil-emulsion vaccine. Ten-day-old SPF embryonated eggs were inoculated with strain YL6 through five passages to yield a titre of 106 to 107 median embryo infectious dose (EID50), which were titrated using the method described by Liu et al (2006a). The harvested viruses were inactivated with 2/1000 formaldehyde for 36 h at 37°C, followed by testing for absence of infectivity by embryo inoculation, adjuvanted with mineral oil in the ratio of 1 to 2 finally.
Eighty 1-day-old SPF White Leghorn chickens were housed in biosecurity isolators under quarantine conditions in Wen's Foodstuff Group Company, and randomly allocated into 4 groups with 20 birds each. The protection effect of live attenuated vaccine XZB (Baoite Biopharmaceutical Corp. Ltd., Qingdao, China; Commercial vaccine, consisted of W93 and H120 strain) and YL6 vaccine were compared through the vaccination-challenge trials. The birds were inoculated intranasally with routine XZB or vaccinated intramuscularly with inactivated vaccine YL6. The detailed vaccination procedures were showed in Table 2. Group 4 was reared as vaccine-negative control.
Blood samples were collected on day 5, 10, 17 and 24. Serum antibody titers of 10 randomly selected chickens from each group were diluted (1: 500) and evaluated with a commercial total antibody ELISA kit (IDEXX Corporation, Westbrook, Maine, USA) as described by Liu et al . Optical density (OD) of each well was read in an ELISA plate reader at 650 nm. Serum-to-positive ratios were calculated, using the formula: SP ratio = (OD sample - OD negative control)/(OD positive control - OD negative control). From these SP ratios, individual serum titres were calculated according to the manufacturer's instructions.
Challenge test was performed in biosafety-level (BSL)-3+ lab after the final antibody test to examine whether or not the novel strain vaccines can provide protective immunity against the relevant infectious viruses. All of the chickens at 24 days old were infected by intranasal instillation of 105 × EID50 of virulent nephropathogenic HY51 strain (GenBank accession numbers: GU938386 for S1 gene) isolated from Heyuan city of Guangdong province (with high morbidity of 100% and mortality of 76%) in May 2009, the strain was belonged to the IBVs of predominant genotype . The chicks were examined daily for signs of infection for 30 days after inoculation. The virus isolation was carried out through tracheal swabs after three weeks post challenge.
Sufficient inactivated oil-emulsion vaccine YL6 was produced as described previously, and applied in some chicken farms in southern China, including Guangdong, Guangxi, Guizhou, Fujian and Sichuan province. In the flocks with epidemic history, the vaccination procedures were as follows, broilers were inoculated intranasally with routine XZB at 5 days of age, and vaccinated intramuscularly with 0.2 ml of inactivated vaccine YL6 at 10 days of age; Broilers were vaccinated intramuscularly with 0.3 ml of YL6 again at 20 days of age. In the non-epidemic flocks, broilers were inoculated with routine XZB at 5 days of age, and immunized with 0.2 ml of vaccine YL6 at 10 days of age.
Cavanagh D, Naqi S: Infectious bronchitis. In Diseases of Poultry. 11th edition. Edited by: Saif YM. Ames: Iowa State University Press; 2003:101-119.
Cook JK, Baxendale W, Greenwood N, Huggins MB, Orbell SJ: Protection of chickens against renal damage caused by a nephropathogenic infectious bronchitis virus. Avian Pathol 2001, 30: 423-426. 10.1080/03079450120066421
Cavanagh D: A nomenclature for avian coronavirus isolates and the question of species status. Avian Pathol 2001, 30: 109-115. 10.1080/03079450120044506
Ji J, Xie J, Chen F, Shu D, Zuo K, Xue C, Qin J, Li H, Bi Y, Ma J, Xie Q: Phylogenetic Distribution and Predominant Genotype of the Avian Infectious Bronchitis Virus in China during 2008-2009. Virol J 2010,8(1):184.
Li L, Xue C, Chen F, Qin J, Xie Q, Bi Y, Cao Y: Isolation and genetic analysis revealed no predominant new strains of avian infectious bronchitis virus circulating in South China during 2004-2008. Vet Microbiol 2010, 143: 145-154. 10.1016/j.vetmic.2009.11.022
Liu S, Chen J, Han Z, Zhang Q, Shao Y, Kong X, Tong G: Infectious bronchitis virus: S1 gene characteristics of vaccines used in China and efficacy of vaccination against heterologous strains from China. Avian Pathol 2006,35(5):394-399. 10.1080/03079450600920984
Liu S, Zhang Q, Chen J, Han Z, Liu X, Feng L, Shao Y, Rong J, Kong X, Tong G: Genetic diversity of avian infectious bronchitis coronavirus strains isolated in China between 1995 and 2004. Arch Virol 2006,151(6):1133-1148. 10.1007/s00705-005-0695-6
Hofstad MS: Cross-immunity in chickens using seven isolates of avian infectious bronchitis virus. Avian Dis 1981, 25: 650-654. 10.2307/1589995
Bing GX, Liu X, Pu J, Liu QF, Wu QM, Liu JH: Different genotypes of nephropathogenic infectious bronchitis viruses co-circulating in chicken population in China. Virus Genes 2007,35(2):333-337. 10.1007/s11262-007-0100-5
Cavanagh D, Ellis MM, Cook JKA: Relationship between variation in the S1 spike protein of infectious bronchitis virus and the extent of cross-protection. Avian Pathol 1997, 26: 63-74. 10.1080/03079459708419194
Gelb J Jr, Keeler CL Jr, Nix WA, Rosenberger JK, Cloud SS: Antigenic and S-1 genomic characterization of the Delaware variant serotype of infectious bronchitis virus. Avian Dis 1997, 41: 661-669. 10.2307/1592158
Liu S, Zhang X, Wang Y, Li C, Han Z, Shao Y, Li H, Kong X: Molecular Characterization and Pathogenicity of Infectious Bronchitis Coronaviruses: Complicated Evolution and Epidemiology in China Caused by Cocirculation of Multiple Types of Infectious Bronchitis Coronaviruses. Intervirology 2009,52(4):223-234. 10.1159/000227134
Xu C, Zhao J, Hu X, Zhang G: Isolation and identification of four infectious bronchitis virus strains in China and analyses of their S1 glycoprotein gene. Vet Microbiol 2007,122(1-2):61-71. 10.1016/j.vetmic.2007.01.006
Mondal SP, Cardona CJ: Genotypic and phenotypic characterization of the California 99 (Cal99) variant of infectious bronchitis virus. Virus Genes 2007,34(3):327-341. 10.1007/s11262-006-0014-7
Liu S, Zhang X, Wang Y, Li C, Liu Q, Han Z, Zhang Q, Kong X, Tong G: Evaluation of the protection conferred by commercial vaccines and attenuated heterologous isolates in China against the CK/CH/LDL/97I strain of infectious bronchitis coronavirus. Vet J 2009,179(1):130-136. 10.1016/j.tvjl.2007.08.018
This work was supported by the Fund from Guangdong Momentously Scientific and Technological Project (Grant No.2009B020201008), strategic cooperation project of GuangdongProvince & Chinese Academy (Grant No. 2010B090301019).
The authors declare that they have no competing interests.
QX and JJ carried out most of the experiments and wrote the manuscript, and should be considered as first authors. JX and FC critically revised the manuscript and the experiment design. MC, BS, CX, JM and YB helped with the experiment. All of the authors read and approved the final version of the manuscript.
Qingmei Xie, Jun Ji contributed equally to this work.
About this article
- Reverse Transcription Polymerase Chain Reaction
- Infectious Bronchitis Virus
- Commercial Vaccine
- Reverse Transcription Polymerase Chain Reaction Assay
- Infectious Bronchitis Virus Strain