CLINICAL OBSERVATIONS AND SIGNIFICANCE OF BHV-1 INFECTION IN SMALLHOLDERS OF CATTLE IN AL-AHSA REGION, KSA

Authors

Dept. of Clinical Studies, College of Vetrinary Medicine and Animal Resources, King Faisal University, KSA.

Abstract

Bovine herpesvirus 1 (BoHV-1), classified as an alphaherpesvirus, is a major pathogen of cattle. Primary infection is accompanied by various clinical manifestations such as infectious bovine rhinotracheitis, abortion, infectious pustular vulvovaginitis, and systemic infection in neonates. In this study A total of 259 animal in small holder cattle sector in Al-Ahsa region, KSA were under investigation form April, 2007 till April 2010.The total number of observed cattle was 259 )159 females and 100 males(. The clinical signs of the disease was observed in 74 (46.6 %) females and 24 (24 %) males. The clinical symptoms are described in both male and female animals as well as young calves. BHV-1 infection was confirmed by isolation and serological identification of the virus. It can be concluded that the sector of smallholders cattle breeding constitutes an important part for cattle production on both dairy and beef cattle in Kingdom Saudi Arabia. The economic losses in this sector due to infectious diseases are really high but unfortunately not estimated. BHV-1 infection in cattle is one of the problems that threads and persist in small holders cattle causing sever economic losses and constitutes a major source of infection to industrial cattle farms. This is probably due to the absence of application of control program for infectious diseases as for example regular  vaccination and isolation of infected animals.
 

Keywords


Dept. of Clinical Studies,

College of Vetrinary Medicine and Animal Resources,

KingFaisalUniversity, KSA.

 

Clinical observations and significance of BHV-1 infection in smallholders of cattle in Al-Ahsa region, KSA

(With 4 Tables)

 

By

F.M.T. Housawi; A. Al-Naeem; E.M.E. Abu-Elzein; A. Afaleq and a.A. Zaghaw

(Received at 15/9/2010)

 

ملاحظات اکلينيکية وأهمية العدوي بفيروس الهربس البقري-1 في الأبقار في تجمعات الأبقار الصغيرة بمنطقة الاحساء بالمملکة العربية السعودية

 

فاضل محمد هوساوي ، عبد المحسن النعيم ، الطيب ابو الزين ، عادل العفالق ، أحمد عبد المنعم زغاوة

 

يعتبر فيروس الهربي البقري-1 المصنف بعائلة فيروسات الهربس من اخطر الأمراض التي تصيب الماشية. تظهر العدوي بهذا الفيروس في صور اکلينيکية متعددة منها: التهاب الأنف والحنجرة- الاجهاض- الالتهاب الحبيبي للاعضاء التناسلية في الذکر والأنثي- العدوي العامة للعجول حديثي الولادة. في هذه الدراسة تم فحص عدد 259 حالة من صغار المربين في منطقة الاحساء بالمملکة العربية السعودية في الفترة من ابريل 2007- ابريل 2010 حيث تمثل هذا العدد ب 159 بقرة و 100 عجل ذکر وعجول رضيعة. سجلت نسية الاصابة بالمرض 74 حالة من الاناث (46.6 %) و 24 حالة في الذکور والعجول الرضيعة 24 حالة (24 %). تم تاکيد العدوي بعزل فيروس الهربس البقري وتصنيفة سيرولوجيا في المعمل. يمکن الخلاصة بان قطاع صغار المربين للماشية في منطقة الاحساء يمثل جزء کبير في انتاج الالبان واللحم. الفخسائر الاقتصادية علي مستوي مربي الماشية الصغار ليست محسوبة رسميا وهي في الواقع کبيرة لذالک فان هذه الدراسة توجب الهتمام بقطاع مربي الماشية علي کل المستويات الصغيرة ووضع سبل للمقاومة مثل عزل الحيوانات المريضة واتباع سياسة التحصين للمرض کما هو متبع في مزارع الالبان الکبيرة.

 

کلمات کشافة:

 (فيروس الهربس البقري-1 والأعراض الاکلينيکية وصغار مربيالماشية وعزل وتصنيف الفيروس)   

 

 

SUMMARY

 

Bovine herpesvirus 1 (BoHV-1), classified as an alphaherpesvirus, is a major pathogen of cattle. Primary infection is accompanied by various clinical manifestations such as infectious bovine rhinotracheitis, abortion, infectious pustular vulvovaginitis, and systemic infection in neonates. In this study A total of 259 animal in small holder cattle sector in Al-Ahsa region, KSA were under investigation form April, 2007 till April 2010.The total number of observed cattle was 259 )159 females and 100 males(. The clinical signs of the disease was observed in 74 (46.6 %) females and 24 (24 %) males. The clinical symptoms are described in both male and female animals as well as young calves. BHV-1 infection was confirmed by isolation and serological identification of the virus. It can be concluded that the sector of smallholders cattle breeding constitutes an important part for cattle production on both dairy and beef cattle in Kingdom Saudi Arabia. The economic losses in this sector due to infectious diseases are really high but unfortunately not estimated. BHV-1 infection in cattle is one of the problems that threads and persist in small holders cattle causing sever economic losses and constitutes a major source of infection to industrial cattle farms. This is probably due to the absence of application of control program for infectious diseases as for example regular  vaccination and isolation of infected animals.

 

Key words: BHV-1, clinical observation, small holder, virus isolation)

 

Introduction

 

Bovine herpesvirus 1 (BoHV-1), classified as an alphaherpesvirus, is a major pathogen of cattle. Primary infection is accompanied by various clinical manifestations such as infectious bovine rhinotracheitis, abortion, infectious pustular vulvovaginitis, and systemic infection in neonates (Muyalkens et al., 2007; Nandi et al., 2009). All BoHV-1 strains isolated hitherto belong to one single viral species, and are classified in three subtypes BoHV-1.1, BoHV-1.2a and BoHV-1.2b. Although most BoHV-1.1 strains have been isolated from respiratory tract diseases or abortive cases and BoHV-1.2 strains from genital organ lesions, the only reliable distinctive criterion is the viral DNA analysis by restriction endonuclease fingerprinting (Edward et al.,1991; Metzler et al., 1985; Miller et al., 1991). Calves infected experimentally by the nasal route with BoHV-1.2 strains showed respiratory clinical signs (Engels et al., 1981; Spilki et al., 2004) and were able to transmit the respiratory infection to control calves (Smith et al., 1980; Edwards et al., 1991). Otherwise, reproductive tract lesions in heifers were observed after intrauterine inoculation with BoHV-1.1 (Miller and Van der Maaten1984). Subtypes 1.1 and 1.2a have been associated with severe diseases including infection of the fetus and abortion (Miller et al., 1991). The subtype 1.2b was not associated with abortion (Whetstone and Miller 1989; Edwards et al., 1990; Smith et al., 1995). BoHV-1 is responsible for significant losses incurred by disease and trading restriction in the cattle industry (Bowland and Shewen, 2000). BoHV-1 is one of the eight herpesviruses isolated hitherto from naturally infected cattle (Tab. I). All members of the family Herpesviridae share a common virion morphology based on an icosahedral capsid symmetry, a cell-derived envelope containing virally encoded membrane proteins and a tegument as protein made matrix connecting the capsid and the envelope. BoHV-1 belongs to the extensive subfamily of Alphaherpesvirinae which contains viruses characterized by a relatively large host range, a short replication cycle and the ability to induce latent infection mainly, but not exclusively, in neurons.

 

Table 1: Herpesviruses isolated from naturally infected cattle after Muyalkens et al. (2007).

 

 

Virus species Disease

Herpesvirus subfamily

Disease following primary infection

Cattle as natural host

Bovine herpesvirus 1 (BoHV-1)

Bovine herpesvirus 2 (BoHV-2)

 

Bovine herpesvirus 4 (BoHV-4)

Bovine herpesvirus 5 (BoHV-5)

Bovine lymphotrophic herpesvirus

 (BLHV)

 

Alpha

Alpha

 

Gamma

Alpha

Gamma

 

 

Infectious bovine rhinotracheitis

Bovine mammillitis

Pseudo lumpy skin disease

Not determined

Bovine herpesvirus encephalitis

Not determined

 

Cattle as foreign host

Alcelaphine herpesvirus 1 (AlHV-1)

Ovine herpesvirus 2 (OHV-2)

Suid herpesvirus 1 (SuHV-1)

 

Gamma

Gamma

Alpha

 

Malignant catarrhal fever

 

Aujeszky’s disease

 

Bovine herpesvirus 5 (BoHV-5) is an alphaherpesvirus responsible for meningoencephalitis in young cattle and is closely antigenically and genetically related to bovine herpesvirus 1 (BoHV-1). Both viruses have common aspects in their pathogenesis: (1) they infect epithelial cells at the portal of entry and (2) they establish a latent infection in the sensory nerve ganglia, i.e., the trigeminal ganglia (Zajac, et al., 2010). The severity of the disease caused by BoHV-1 is influenced by several factors such as the virulence of the BoHV-1 strain (Kaashoek et al., 1996), resistance factors of the host, especially the age, and potential concurrent bacterial infection. Subclinical BoHV-1 infections are common. Several BoHV-1 strains display a poor ability to induce clinical signs and were classified as weakly virulent strains in a comparative virulence experiment (Kaashoek et al., 1996). Otherwise, these discrete clinical pictures can also be explained by the primary infection of passively immune calves in countries where BoHV-1 is endemic. Indeed, colostral immunity is known to protect efficiently infected animals from clinical signs (Mechor et al., 1987; Lemaire et al., 2000). The latency reactivation cycle of herpesviruses has a deep epidemiological impact since it is responsible for the maintenance of BoHV-1 in a cattle population. BoHV-1 infection of new generation cattle by latent carriers submitted to reactivation stimulus may occur at several occasions as for example at birth (Spilki et al., 2004), mating, during transport (Thiry et al., 1987) or following the introduction of heifers into the group of dairy cows. Therefore the detection of BoHV-1 latent carriers is a concern in the setting up of a BoHV-1 control program.

The sector of smallholders in cattle breeding constitutes an important part for cattle production on both dairy and beef cattle in Kingdom Saudi Arabia. The aim of the present work was planned to fulfill the followings: recording and investigate the clinical observations of BHV-1 in smallholders cattle in Al-Ahsa` region, KSA, collection of information about current control program in this sector, confirmation  of clinical cases through virus isolation and identification, and finally recommendation to control the disease in smallholders cattle in KSA.

 

Materials and Methods

 

1- Animals:

The description of the animals is very difficult because they collected from different small system that has irregular management system and there were no confirmed data about any other infection during the period of observation.

A total of 259 animal were under investigation form April, 2007 till April 2010. Details of information are found in the Table (2). 

 

 

Table 2: Animals under  investigation

 

 

Year

Total Animal examined

 

Sex

Age average

2007

24

18 males &

 6 female

3 years

3.5 years

2009

70

42 males &

28 females

3 years

3.5 years

2010

165

99 males &

66 females

3 years

3.5 years

4 animals under sex months

Total

259

159 males &

100 female

3 years

3.5 years

4 animals under sex months

 

2 - Virus isolation and identification:

Buffy coat were collected from feverish animals and inoculated into MDBK cell line in which the monlayer cell culture were grown on Eagl s MEM supplemented with 3 % newborn calf serum. After 48 hours positive samples showed cytopathogenic effect in the cell line that begins with cell rounding that advances to for grape-like structures, beside the formation of synthetial cell (Giant cells).

For confirmation of the specificity of CPE, specific antiserum to BHV-1 (Kindly Supplied by Institute of Virology, Hannover Veterinary School, Germany) was added to the buffy coats and incubated for 30 minutes at 37°C before inoculation to the cell culture. Colorado strain of BHV-1 kindly supplied by Institute of Virology, Hannover Veterinary School, Germany was used as positive control. The CPE were inhibited in both positive samples and the positive control.

3 - Sero-conversion:

Antibodies to BHV-1 were detected in the sera of convalescent animals using a commercial ELISA kits produced by Institute Pourquier, France.

 

Results and Discussion

 

Bovine herpesvirus 1 (BoHV-1),is  a pathogen of cattle associated with two major syndromes, called infectious bovine rhinotracheitis (IBR) and infectious pustular vulvovaginitis (IPV), and a variety of clinical signs, such as conjunctivitis, encephalitis and abortions (Pastoret et al., 1982). IBR is a disease of major economic concern in many parts of the world band especially in Europe, both in countries where this infection has been eradicated and in those where the control of IBR is currently or will be undertaken (Thiry et al., 1999). Table (3) describes the different clinical symptoms of BHV-1 infection observed in smallholder cattle in Al-Ahsa region, KSA. The table summarizes the main items of symptoms with the percentage in the clinical diseased animals. The described symptoms are quite the same that recorded by many authors (Gibbs and Rweyemamu, 1977; Millerand Van der Maaten1986; Bryan et al., 1994; Hage et al., 1998; Radostitis et al., 2007; Muylkens et al., 2007 and Nandi et al., 2009). Table (4) illustrates the percentage of clinical disease of BHV-1 in small holder cattle in Al-Ahsa region, KSA during 3 years observation (April, 2007- April, 2010). The total number of observed cattle was 259 from which 159 females and 100 males. The clinical disease was observed in 74 (46.6 %) females and 24 (24 %) males. Serological evidence of BHV-1 infection in dairy cattle in Kingdom Saudi Arabia was recorded by Frericks et al. (1982) and (1983). The isolation of the BHV-1 from dairy cattle in Kingdom Saudi Arabia was confirmed by Hafez and Chaudry (1985). The emergence of clinical infectious bovine rhinotracheitis in the eastern region of the Kingdom Saudi Arabia was recorded for the first time by Abu-Elzein et al. (2008). They suggested that the source of the outbreak could be due to the reactivation of a latent infection. This is highly likely, as there was no recent introduction of new animals in the affected farm. On the other hand, results of the limited serological survey on the non-vaccinated, apparently healthy 14 cattle from the affected herd indicated that a high percentage (50%) were exposed to IBR infection and that some of them gave high BP values which were comparable with the reference positive serum. As no cattle were recently introduced into the farm, this high seroconversion rate could most probably indicate shedding of the IBR virus by carrier cattle in the herd. The sector of smallholders in cattle breeding constitutes an important part for cattle production on both dairy and beef cattle in Kingdom Saudi Arabia. The absence of clear regulation in this sector makes difficulty in controlling infectious diseases. On the same time the economic losses (due to mortality in newborn animals, abortion and others) in this sector due to infectious diseases are really high but unfortunately not estimated. BHV-1 infection in cattle is one of the problems that threads and persist in small holder cattle causing sever economic losses and constitutes a major source of infection to industrial cattle farms. This is probably due to the absence of application of control program for infectious diseases as for example regular  vaccination and isolation of infected animals.

 

Table 3: Different clinical symptoms observed in 98 cattle infected with BHV-1 virus.

 

 

                                    Clinical symptom

 

Number of animal

% in diseased animal

1) Fever (up to 42ºc) with anorexia

92

93.88 %

2) Sever hyperemia of nasal mucous membrane

83

84.69 %

3) Serous nasal discharge from eyes and nose

66

67.35 %

4) Increased salivation

52

53.06 %

5) Grayish foci of necrosis on the mucous membrane of the nasal septum inside the external nares.

81

82.65 %

6) A drastic fall in milk yield

20

20.41 %

7) A short, explosive cough

16

16.33 %

8) Uni-or bilateral conjunctivitis

25

25.51 %

9) Erosions covered with tenacious mucous of soft palate

14

14.29%

10) Pharyngitis with tenacious mucopurulent exudates

28

28.57 %

11) Bronchopneumonia (loud breath sound, crackles and wheezes)

18

18.37 %

12) Abortion, retention of placenta  and Endometritis

6

6.12 %

13) Necrotic lesions on the mucosa of vulva and vagina of cows, penis and prepuce of bulls, they  are gray translucent raised foci, erode, ulcerate and become confluent

34

34.69 %

14) Obvious signs of pain (arched back holding the tail out stiffly( and frequent urination

12

12.24 %

 

Table 4: Percentage of clinically diseased animals by BHV-1 in smallholder cattle in Al-Ahsa region, KSA.

 

Year

 

Total Animal examined

Sex

Age average

Number of diseased animals

Percentage of clinical disease

2007

24

18 males &

6 female

3 years

 

3.5 years

16

 

4

88.9 %

 

66.7 %

2009

70

42 males &

28 females

3 years

3.5 years

25

 

11

59.5 %

 

39.3 %

2010

165

99 males &

66 females

3 years

3.5 years

4 animals under sex months

33

9

33.3 %

13.6 %

Total

259

159 males &

100 female

3 years

3.5 years

4 animals under sex months

74

24

46.5 %

24 %

 

Acknowledgement

 

We acknowledge the Deanship of Scientific research, KingFaisalUniversity for the support to fulfill this research work (Project Number: 5022) for the academic year 1427-1428.

 

References

 

Abu Elzein, E.M.E.; Housawi1, F.M.T.; Al-Afaleq1, A.I. and Al-Musa1, J. (2008): Emergence of Clinical Infectious Bovine Rhinotracheitis in Eastern Saudi Arabia. Revue Élev. Méd. Vét. Pays trop., 61 (1): 11-13.

Bowland, S.L. and Shewen, P.E. (2000): Bovine respiratory disease: commercial vaccines currently available in Canada, Can. Vet. J. 41: 33–48.

Bryan, L.A.; Fenton, R.A.; Misra, V. and Haines, D.M. (1994): Fatal, generalized bovine herpesvirus type-1 infection associated with a modified-live infectious bovine rhinotracheitis parainfluenza-3 vaccine administered to neonatal calves, Can. Vet. J. 35:223–228.

Edwards, S.; White, H. and Nixon, P. (1990): A study of the predominant genotypes of bovid herpesvirus 1 found in the UK, Vet. Microbiol. 22: 213–223.

Edwards, S.; Newman, R.H. and White, H. (1991): The virulence of British isolates of bovid herpesvirus 1 in relationship to viral genotype, Br. Vet. J. 147: 216–231.

Engels, M.; Steck, F. and Wyler, R. (1981): Comparison of the genomes of infectious bovine rhinotracheitis and infectious pustular vulvovaginitis virus strains by restriction endonuclease analysis, Arch. Virol. 67: 169–174.

Frericks, W.M.; Barbour, F.M.; Al-Rasheed, A. and Hafez, S.M. (1982): Infectious bovine rhinotracheitis and salmonellosis in Saudi Arabian dairy herd. In: Proc. 12th World Congress on Diseases of Cattle, Amsterdam, Netherlands, 7-10 Sept. 1981, p. 1007-1011.

Frericks, W.M.; Hafez, S.M. and Al-Rasheed, A. (1983): Serological evidence for the occurrence of IBR in Saudi Arabia. In: 6th Symp. Biol. Aspt., Jeddah, Saudi Arabia, p. 54.

Hafez, S.M. and Chaudry, R. (1985): Isolation and identification of IBR virus in Saudi Arabia. ArabGulf J. Sci. Res., 3: 735-744.

 

 

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Kaashoek, M.J.; Straver, P.H.; Van, R.E.; Quak, J. and Van Oirschot, J.T. (1996): Virulence, immunogenicity and reactivation of seven bovine herpesvirus 1.1 strains: clinical and virological aspects, Vet. Rec. 139: 416–421.

Lemaire, M.; Weynants, V.; Godfroid, J.; Schynts, F.; Meyer, G.; Letesson, J.J. and Thiry, E. (2000): Effects of bovine herpesvirus type 1 infection in calves with maternal antibodies on immune response and virus latency, J. Clin. Microbiol. 38: 1885–1894.

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Metzler, A.E.; Matile, H.; Gassmann, U.; Engels, M. and Wyler, R. (1985):  European isolates of bovine herpesvirus 1: a comparison of restriction endonuclease sites, polypeptides, and reactivity with monoclonal antibodies, Arch. Virol. 85: 57–69.

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Miller, J.M. and Van der Maaten, M.J. (1986): Experimentally induced infectious bovine rhinotracheitis virus infection during early pregnancy: effect on the bovine corpus luteum and conceptus, Am. J. Vet. Res. (1986) 47: 223–228.

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References
 
Abu Elzein, E.M.E.; Housawi1, F.M.T.; Al-Afaleq1, A.I. and Al-Musa1, J. (2008): Emergence of Clinical Infectious Bovine Rhinotracheitis in Eastern Saudi Arabia. Revue Élev. Méd. Vét. Pays trop., 61 (1): 11-13.
Bowland, S.L. and Shewen, P.E. (2000): Bovine respiratory disease: commercial vaccines currently available in Canada, Can. Vet. J. 41: 33–48.
Bryan, L.A.; Fenton, R.A.; Misra, V. and Haines, D.M. (1994): Fatal, generalized bovine herpesvirus type-1 infection associated with a modified-live infectious bovine rhinotracheitis parainfluenza-3 vaccine administered to neonatal calves, Can. Vet. J. 35:223–228.
Edwards, S.; White, H. and Nixon, P. (1990): A study of the predominant genotypes of bovid herpesvirus 1 found in the UK, Vet. Microbiol. 22: 213–223.
Edwards, S.; Newman, R.H. and White, H. (1991): The virulence of British isolates of bovid herpesvirus 1 in relationship to viral genotype, Br. Vet. J. 147: 216–231.
Engels, M.; Steck, F. and Wyler, R. (1981): Comparison of the genomes of infectious bovine rhinotracheitis and infectious pustular vulvovaginitis virus strains by restriction endonuclease analysis, Arch. Virol. 67: 169–174.
Frericks, W.M.; Barbour, F.M.; Al-Rasheed, A. and Hafez, S.M. (1982): Infectious bovine rhinotracheitis and salmonellosis in Saudi Arabian dairy herd. In: Proc. 12th World Congress on Diseases of Cattle, Amsterdam, Netherlands, 7-10 Sept. 1981, p. 1007-1011.
Frericks, W.M.; Hafez, S.M. and Al-Rasheed, A. (1983): Serological evidence for the occurrence of IBR in Saudi Arabia. In: 6th Symp. Biol. Aspt., Jeddah, Saudi Arabia, p. 54.
Hafez, S.M. and Chaudry, R. (1985): Isolation and identification of IBR virus in Saudi Arabia. ArabGulf J. Sci. Res., 3: 735-744.
 
 
Hage, J.J.; Schukken, Y.H.; Dijkstra, T.; Barkema, H.W.; Van Valkengoed, P.H. and Wentink, G.H. (1998): Milk production and reproduction during a subclinical bovine herpesvirus 1 infection on a dairy farm, Prev. Vet. Med. 34: 97–106.
Gibbs, E.P.; and Rweyemamu, M.M. (1977): Bovine herpesviruses. PartI. Bovine herpesvirus 1, Vet. Bull. 47: 317–343.
Kaashoek, M.J.; Straver, P.H.; Van, R.E.; Quak, J. and Van Oirschot, J.T. (1996): Virulence, immunogenicity and reactivation of seven bovine herpesvirus 1.1 strains: clinical and virological aspects, Vet. Rec. 139: 416–421.
Lemaire, M.; Weynants, V.; Godfroid, J.; Schynts, F.; Meyer, G.; Letesson, J.J. and Thiry, E. (2000): Effects of bovine herpesvirus type 1 infection in calves with maternal antibodies on immune response and virus latency, J. Clin. Microbiol. 38: 1885–1894.
Mechor, G.D.; Rousseaux, C.G.; Radostits, O.M.; Babiuk, L.A. and Petrie, L. (1987):Protection of newborn calves against fatal multisystemic infectious bovine rhinotracheitis by feeding colostrum from vaccinated cows, Can. J. Vet. Res. 51: 452–459.
Metzler, A.E.; Matile, H.; Gassmann, U.; Engels, M. and Wyler, R. (1985):  European isolates of bovine herpesvirus 1: a comparison of restriction endonuclease sites, polypeptides, and reactivity with monoclonal antibodies, Arch. Virol. 85: 57–69.
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