Variations in Pathogenicity and Molecular Characterization of Infectious Bursal Disease Virus (IBDV) in Egypt

Introduction

The Infectious Bursal Disease Virus (IBD/IBDV) or Gumboro Disease is an acute highly contagious viral disease of young chickens characterized by a hemorrhagic syndrome, severe damage in cloacal bursa, immunosuppression and high mortality generally at 3 to 6 weeks of age (Eterradossi and Saif, 2013). IBD was first reported in 1957 in Southern Delaware town of Gumboro, U.S.A (Cosgrove, 1962; Parkhurst, 1964). It is one of the most economical important diseases that affects commercially produced chickens worldwide (Müller et al., 2003). IBDV is classified as a member of the family Birnaviridae and genus Avibirnaviridae. Its genome consists of 2 segments of double-stranded RNA (dsRNA) and characterized by non-enveloped icosahedral capsid (Leong et al., 2000). Two serotypes of the virus have been described; Serotype1 IBDV strains, pathogenic to chickens (Van den Berg et al., 2004), whereas serotype 2 strains are non-pathogenic (McFerran et al., 1980). In Egypt, El-Sergany et al. (1974) diagnosed the IBD for the first time on the basis of its specific pathological lesions. Very virulent IBDV were reported since its first introduction in 1989 in vaccinated Egyptian flocks by El- Batrawi (1990). RT-PCR has been useful in detecting IBDV serotypes and to a lesser extent, differentiating IBDV subtypes. Amplifying the VP2 hypervariable region, in combination with DNA sequencing of the PCR product, can differentiate classic, variant and vvIBDV strains because variant and vvIBDV have characteristic nucleotide and amino acid substitutions. This approach is a valuable tool for molecular epidemiological studies on IBDV (Islam et al., 2012). The Hyper Variable Region (HVR) on VP2 (206-350 Amino Acid) contains the most informative genetic data regarding strain variability, it was chosen for sequence analysis to characterize IBDV strains molecularly, allowing analysis of variations that happen naturally or by attenuation in different strains, leading to changes in antigenicity and/or virulence (Jackwood et al., 2008). The IBD infection consider one of the immunosuppressive disease which can be predisposing factor for other bacterial or viral pathogen or failure in inactivated vaccine application, E. coli infection can associated with the IBD infection and cause economic losses in poultry flocks (Eid et al., 2016). Immunosuppression effect can alter the immune modulator specially pathogen recognition receptor pathways which intern can affect the general immune response to different pathogens (Abouelmaatti et al., 2013; Elfeil et al., 2012; 2016). The pathogenicity of IBDV isolates was evaluated by experimental infection of susceptible chickens based on clinical signs, mortality, gross lesions, Bursa: Body weight index and histopathological analysis of the bursa of Fabricius (Jackwood et al., 2011). This study aims to investigate the variations in pathogenicity and molecular characterization of IBDV in Egypt.

Materials and Methods

Field Samples

A total number of 26 chicken farms were investigated for IBD outbreak over the period of 2015-2016. Bursal samples were collected and processed to prepare a bursal homogenate. About 10% tissue suspensions were prepared as described by Hirai and Shimakura (1974).

Virus Isolation

The tissue suspensions were used for virus isolation by inoculation in 9-11 days embryonated chicken eggs via CAM. The allantoic fluids were collected for applying rapid slide haemagglutination test as reported by Wlliams (2016).

Molecular Identification by RT-PCR

RNAs were extracted from pools of CAM and embryo cell extract of 26 field isolates using QIAamp Viral RNA Mini Kit (Qiagen, Valencia, USA). Cat. No.52904. the procedure was performed according to the company's instruction. A set of primers were used: Forward primer: [AUS GU: 50-TCA CCG TCC TCA GCTTAC CCA CAT C-30]. Reverse primer: [AUS GL: 50-GGA TTT GGG ATC AGCTCG AAG TTG C-30] (Metwally et al., 2009).

Sequence Analysis of HVR of VP2 Gene

Gel containing DNA band of the expected size (620 bp) was excised and purified with the QIA quick Gel Extraction Kit (Qiagen) according to the manufacturer instruction. The purified PCR products were sequenced directly using big dye Terminator V3.1 cycle sequencing kit (Perkin-Elmer, Foster city, CA, USA). The phylogram was drawn using also MEGA 5 software. The alignment of the viruses in the study was done using DNA star- MegAlign software. Egyptian viruses and other international reference strains from the Genbank and were available from the National Center for Biotechnology Information (NCBI) infectious bursal disease viruses’ resource (http://www.ncbi). Finally, the identity percent and divergence between all viruses was carried out.

Determination of EID50 of 6-Selected IBDV Field Isolates

Titration of selected IBDV field isolates no. (21, 22, 23, 24, 25 and 26) was carried out and the EID50 was calculated according to Reed and Muench (1938).

Pathogenicity Experiment

Hundred and five SPF chicks were reared in previously fumigated house, provided with food and water ad libitum. This study was carried out in strict accordance with the recommendations of the Committee on the Ethics of Animal Experiments of Alexandria University, Egypt. All procedures and experiments complied with the guidelines and were approved by the Local Ethic Commission of the Animal Experiments of Alexandria University with respect to animal experimentation and care of animals under study. All efforts were made to minimize suffering. At 21st day-old, the chickens were divided into 7 groups, each contain 15 birds and housed separately in strictly isolated disinfected rooms. The chickens were experimentally infected (Groups 1-6 were infected with 6-selected IBDV positive field isolates naso- ocular with 0.1 mL of EID50 but Group-7 kept as non- infected control group)as shown in Table 1.

Variations in Pathogenicity and Molecular Characterization of Infectious Bursal Disease Virus (IBDV) in Egypt - Image 1

Variations in Pathogenicity and Molecular Characterization of Infectious Bursal Disease Virus (IBDV) in Egypt - Image 2

All groups kept under daily observation for 10 days post infection and clinical signs, mortality rate, PM lesions; body and bursal weight were recorded.

Calculation of Bursal Body Weight Index

Bursal body weight ratio and BB index were calculated according to the formulas of Lucio and Hitchner (1979):

Variations in Pathogenicity and Molecular Characterization of Infectious Bursal Disease Virus (IBDV) in Egypt - Image 3

Chickens with BB index lower than 0.7 were considered to have bursal atrophy (Lucio and Hitchner, 1979).

Calculation of EID50 of 6-Selected Field Isolates

The egg-infected dose 50 calculated for six-selected infectious Bursal Disease virus (IBD) as shown in Table 2.

Histopathological Examination

Five Bursae from freshly dead or sacrificed birds collected at 3th and 7th day post infection from each group, Tissue specimen fixed in 10% neutral buffered formalin solution for at least 24 h. The fixed specimens were processed through the conventional paraffin embedding technique (Culling, 1974). Paraffin sections of 5 µm thickness were prepared and stained with (H& E stain) then examined under optical microscope.

Results

IBDV Isolation in Embryonated Chicken Eggs (ECE)

Mortality patterns of infected embryos were varied between 0-100%, Rapid slide HA test proved that the allantoic fluids of all field isolates were negative for hemagglutininating agents. Embryos which died from 3- 7 days post inoculation showed some gross pathological lesions as abdominal and/or cerebral edema, dwarfing, cutaneous congestion and hemorrhages particularly along feather tracts, in cerebral region and toe joints, mottled-appearing necrosis and congestion of liver sometimes with a greenish discoloration, congested kidney, pale heart and enlarged spleen and Sometimes CAM had hemorrhagic areas.

Molecular Characterization of IBDV Field Isolates: Reverse Transcriptase-Polymerase Chain Reaction (One-Step RT-PCR)

There were 11 out of 26 field isolates were positive RT-PCR with a percent of 42.3% (5 out of 12 in ElBehera; 3 out of 7 in Kafr El-sheikh; 1 in Marsa Matrouh and 2 out of 6 in Alexandria with a percent of 41.6%; 42.8%; 100% and 33.3% respectively). Eleven RT-PCR positive isolates were detected in 2 layers farms (40%), 4 native baladi farms (57.1%) and 5 broilers farms (35.7%) as shown in Table 3 and Fig. 1.

Sequencing and Phylogenic Analysis

Sequence analysis of HVR of VP2 of 11 IBDV isolates was conducted and revealed that all isolates were highly genetically related and have amino acid identity between each other (73.8-100%), between Egyptian vvIBDV (Giza 2008) strains (80.6-97.5%) but when compared with classical vaccinal strains it showed (74.4-95.6%) identity as shown in Fig. 2. From the phylogenetic tree, it was found that all isolates were clustered together and closely related to previous isolated vvIBDV strains from Egypt (Fig. 2). From the phylogenetic tree, it was found that all isolates were clustered together and closely related to previous isolated vvIBDV strains from Egypt (Fig. 3).

Determination the Pathogenicity of 6-Selected IBDV Field Isolates

All chickens were observed for 10 days post infection, clinical signs, mortality rates, gross lesions, body weight, bursal weight, bursal body weight ratio and bursal body weight index were recorded.

Clinical Signs, Mortality and Gross Lesions Post Infection

Groups (1-6) induced 80-100% morbidity; clinical signs appeared suddenly at 2nd day post-infection in form of depression, anorexia, ruffled feathers, huddling, tremors, prostration, whitish watery diarrhea and soiled vent. Groups (2, 3, 4 and 5) showed more severe clinical signs than other groups. Mortality started from third to 6th days post-infection (26.7-80%). The highest mortality rates were appeared in groups 2, 3, 4, 5 with percentage of 60%, 80%, 46.7% and 40% receptively. The lowest mortality rate appeared on groups (1 and 6) with percentage of 33.5% and 26.7% receptively. The control negative Group (7) appeared normal throughout observation period. The pattern of mortality during observation period is presented in Table 4. The lesions included dehydration, difficult separation of skin on abdominal muscle, congestion and hemorrhages on thigh (groups 1, 3, 4 and 5) and abdominal muscles (groups 4 and 5); hemorrhage at junction between proventriculus and gizzard (Groups 2, 3, 4 and 5); infarcted and darken discolored liver; swollen kidney with petechial hemorrhage and ureters filled with urates. The bursa of Fabricius was enlarged, edematous with gelatinous yellow transudate covering serosal surface at 3rd/4th days post infection, sometimes hemorrhagic, or atrophied in most dead or sacrificed birds at 7th day post infection. Spleen appeared enlarged or congested in some cases. Bursa/body weight ratio and bursa/body weight index at 7th day post infection were calculated at 7th day post-infection (Fig. 4).

Variations in Pathogenicity and Molecular Characterization of Infectious Bursal Disease Virus (IBDV) in Egypt - Image 4

Variations in Pathogenicity and Molecular Characterization of Infectious Bursal Disease Virus (IBDV) in Egypt - Image 5

Variations in Pathogenicity and Molecular Characterization of Infectious Bursal Disease Virus (IBDV) in Egypt - Image 6

Variations in Pathogenicity and Molecular Characterization of Infectious Bursal Disease Virus (IBDV) in Egypt - Image 7

Variations in Pathogenicity and Molecular Characterization of Infectious Bursal Disease Virus (IBDV) in Egypt - Image 8

Variations in Pathogenicity and Molecular Characterization of Infectious Bursal Disease Virus (IBDV) in Egypt - Image 9

Variations in Pathogenicity and Molecular Characterization of Infectious Bursal Disease Virus (IBDV) in Egypt - Image 10

The Average Bursa and Body Weight Index

The calculated average bursa weight to bird body weight and detected ration showed in Table 5. The calculated bursa and body weight index in dead and scarified birds at the 7th day post infection showed in Table 5.

Histopathological Examination

The histopathological Bursal changes in infected groups at 3rd and 7th days post infected were shown in Fig. 5.

Discussion

HI In the current study, Virus isolation of bursal suspension in SPF embryonated chicken eggs was carried out to confirm the presence of the etiological and the picture in embryonated chicken eggs matched with the IBD lesions. The embryo mortalities were varied between 0-100%, dead embryos showed typical IBDV gross lesions; These embryonic changes were in agreement with Rosenberger et al. (1998). The histopathological Bursal changes in infected groups at 3^rd and 7^th days post infected were matches with IBD typical lesions where The bursa of Fabricius of chickens in group-1 during 3^rd day showing lymphoid depletion, sub- epithelium edema (A), atrophy of the follicles (stars) and presence of cystic cavity formation of follicles as shown in Fig. 5a. The bursa of Fabricius of chickens in group-2 during 3^rd day showing lymphoid depletion with proliferating interfollicular connective tissue (A) and desquamation of bursal epithelium (stars) as shown in Fig. 5b. The bursa of Fabricius of chickens in group-3 during 3^rd day showing lymphoid depletion, atrophy of the follicles, stromal edema (A) and associated with inflammatory response (stars) as shown in Fig. 5c. The bursa of Fabricius of chickens in group-4 during 3^rd day showing lymphoid depletion with proliferating interfollicular connective tissue and sub epithelium edema as shown in Fig. 5d. The bursa of Fabricius of chicken in group-5 of during 3^rd day showing the most of follicles medulla replaced with eosinophilic material (stars) as shown in Fig. 5e. The bursa of Fabricius of chicken in group-6 during 3^rd day showing mild lymphoid depletion and widening of medulla (M) at the expanse of cortex as shown in Fig. 5f. The bursa of Fabricius of chicken in the control negative group during 3^rd day showing normal histological structure of cortex (C) and medulla (M) as shown in Fig. 5g. The bursa of Fabricius of chicken group-1 during 7^th day showing lymphoid depletion and necrosis of the follicles (stars) as shown in Fig. 5h. The bursa of Fabricius of chicken in group- 2 during 7^th day showing lymphoid depletion with proliferating interfollicular connective tissue; beside inflammatory cell infiltrations (A) as shown in Fig. 5k. The bursa of Fabricius of chicken in group-3 during 7^th day showing lymphoid depletion, atrophy of the follicles, stromal edema and fibrosis (A) and associated with inflammatory response with presence of cystic cavity formation of follicles as shown in Fig. 5m. The bursa of Fabricius of chicken in group-4 during 7^th day showing lymphoid depletion with proliferating interfollicular connective tissue beside inflammatory cell infiltrations as shown in Fig. 5n. The bursa of Fabricius of chicken in group-5 during 7^th day showing lymphoid depletion, sub-epithelium edema (A) and atrophy of the follicles as shown in Fig. 5o. The bursa of Fabricius of chicken in group-6 during 7^th day showing lymphoid depletion with proliferating interfollicular connective tissue as shown in Fig. 5p. The bursa of Fabricius of a chicken of the control negative group during 7^th day showing normal histological structure of cortex (C) and medulla (M) as shown in Fig 5q. The RT-PCR consider a useful and sensitive test in detecting IBDV serotypes, in the present study, RT-PCR was used to amplify a 620 bp fragment length within IBDV on VP2 gene from bursal samples and found that 11 out of 26 field isolates were positive by RT-PCR with a percent of 42.3%; which confirmed the embryonated chicken egg isolation steps and the obtained results from this step matched with Similar study was carried by Mawgod et al. (2014). In this study, a comparative alignment and phylogenetic analysis of the hypervariable domain of the VP2 revealed that all isolates were highly genetically related, have amino acid identity between each other (73.8-100%) and between Egyptian vvIBDV (Giza 2008) strain (80.6-97.5%) identity but when compared with classical vaccinal strains it showed (74.4-95.6%) identity. This amino acid substitution may affect virus antigenicity change which may has an important role in increasing virulence that may cause disease in the presence of high maternal antibody. In this study, all isolates show the same amino acids at position 222 A, 242I, 253 G, 256 I, 279D, 284 A, 294 I, 299S and 330 S except 451 L not involved in the sequenced fragment in this study this findings agreed with Jackwood et al. (2008) Residues present in the VP2 region at position (P222A), (V242I), (G253Q), (V256I), (N279D), (T284 A), (L294I) and (N299S, (R330S) and 451 (L)) reported to be unique for all vvIBDV strains as compared to classical strains (Van den Berg et al., 2004). Strains that have glutamine at position 253 reported to be high pathogenicity than those with a histidine at position 253 were much less pathogenic. A glutamine residue at position 253 was found in the eleven isolates examined in our study as well as the previously isolated Giza 2008, Giza 2000 IBDV indicating high pathogenicity. These results agreed with Brandt et al. (2001) who reported that reverse genetic experiments have shown that the amino acid at position 253in VP2 affects the virulence of IBDV.

Variations in Pathogenicity and Molecular Characterization of Infectious Bursal Disease Virus (IBDV) in Egypt - Image 11

The serine rich heptapeptide SWSASGS (326-332) located immediately downstream of the second hydrophilic region was believed to be involved in the virulence of IBDV (Heine et al., 1991). At this study presence of typical heptapeptide (SWSASGS) in the eleven examined samples indicating that they were pathogenic strains. This was in agreement with Heine et al. (1991). The presence of the specific SspI restriction site on VP2 corresponds to the substitution at residue (leucine L 294I isoleucine) was previously reported to be characteristic of vvIBDV strains (Jackwood et al., 2008). All vvIBDV isolates under study had this restriction site while it was not observed in vaccine (classic) strain. Results of this study agreed with Mawgod et al. (2014). The results of this study, speculate that, the isolated strains are highly related to vvIBDV strains belonging to serotype-1 isolates and indicating that they were pathogenic strains and that vvIBDV belong to Egyptian strains succeeded in surviving in the Egyptian environment despite the intensive use of vaccination programs. This observation agreed with Mawgod et al. (2014). The titre of six characterized IBDV field isolates ranged from 10^-3.5 to 10^-4.8 EID₅₀/0.1 mL homogenate and the infective dose per isolate used in pathogenicity test was 0.1 ml EID₅₀/bird (Sultan et al., 2012). Experimentally infected chickens induced 80-100% morbidity. The mortality rate varied from 26.7 up to 80%, suggested that all isolates were probably of the vvIBDV pathotype. Presence of vvIBDV strains in Egyptian environment were reported also by Metwally et al. (2009). The bursa /body weight index of all infected groups in comparison with non-infected control showed different degrees of bursal atrophy (<0.7). Bursal atrophy 7 days post infection was supported by Hussein (2006), who mentioned that bursal atrophy began at 5-8 days post infection. In this study, the histopathological findings were characteristic to vvIBDV infection. All isolates induced bursal lesions, which began at 3^rd day post infection and continued to day 7 post-infection. The lesions were severe in groups -2, -3 and -4; moderate in groups -1 and -5 and mild in group-6. The bursae of fabricius of control negative group showing normal histological structure. The results of this study were in agreement with the results obtained by Jackwood et al. (2011).

Conclusion

The present study concluded that the circulating strains were highly related to vvIBDV strains belonging to serotype-1 isolates and indicating that they are highly pathogenic to 21-day-old SPF chickens and that vvIBDV strains succeeded in surviving in the Egyptian farms despite of the application of intensive vaccination programs.

Acknowledgement

Author acknowledge the support from Alexandria University

Conflicts of Interest

All authors have no conflict of interest.

This article was originally published in American Journal of Animal and Veterinary Sciences 2018, 13 (2): 76.86 DOI: 10.3844/ajavsp.2018.76.86. This is an Open Access article distributed under a Creative Commons Attribution (CC-BY) 3.0 license.