Seroprevalence of Bovine Herpesvirus Type 1 Among the Cattle Population in Iran: A Systematic Review and Meta-Analysis

Document Type : Review Article

Authors

1 D.V.M., UnFaculty of Veterinary Medicine, University of Tehran, Tehran, Iran.

2 School of Animal and Veterinary Sciences, The University of Adelaide, Adelaide, Australia.iversity of Tehran, Tehran, Iran

Abstract

Bovine herpesvirus type 1 (BHV-1) is the causative agent of several clinical manifestations, including infectious bovine rhinotracheitis, infectious pustular vulvovaginitis/balanoposthitis, conjunctivitis, encephalitis, abortion, infertility, mastitis, enteritis, dermatitis, and the systemic form of the infection in newborn calves. Although many investigations regarding the prevalence of BHV-1 infection in cattle in Iran have been conducted, until now there has been a lack of comprehensive information on the BHV-1 status in Iran. We aimed to present the seroprevalence of BHV-1 in the cattle population in Iran based on a systematic review and meta-analysis study and also to give useful outputs in formulating the infection-control strategies. The meta-analysis study was conducted using national and international databases to find articles which evaluated BHV-1 seroprevalence by antibody-capture enzyme linked immono sorbert assay (ELISA) in cattle in Iran by searching terms including Bovine herpesvirus type 1, cow, cattle, bovine, Iran, epidemiology, and prevalence alone or in combination in both English and Farsi languages. After reviewing 124 published documents, a total of 25 studies from 20 documents were eligible to be included in this meta-analysis study. The analysis was performed using the Comprehensive Meta-Analysis software, VERSION 3. The total seroprevalence of BHV-1 in apparently healthy cattle at the animal and herd levels based on the ELISA test was 40.2% (95% CI, 32.3%, 48.6%) and 75.5% (95% CI, 63.9%, 84.2%), respectively. A well-defined control strategy for preventing and controlling BHV-1 infection in Iran should be based on further studies on BHV-1 epidemiology, control of animal and semen importation, the use of marker vaccines, and planned biosecurity measures to control the epidemiological risk of infection due to the presence of BHV-1 latent carriers.

Keywords

Main Subjects


1. Context

Bovine herpesvirus type 1 (BHV-1) is an enveloped DNA virus, a member of the genus Varicellovirus in the subfamily Alphaherpesvirinae, which belongs to the Herpesviridae family in the order Herpesvirales. Based on genomic analyses and viral peptide patterns, four different serotypes of BHV-1 have been characterized, of which the respiratory subtype BHV-1.1 is associated with respiratory disease, subtypes BHV-1.2a and BHV-1.2b are related to genital disease, and BHV-1.3 is related to neurological disorders and has been reclassified as three genotypes, BHV-5a, BHV-5b, and BHV-5non-a/non-b [ 1 - 3 ].

The virus is the cause of multiple clinical signs in cattle populations worldwide; however, other Artiodactyla may be infected with BHV-1 and show clinical signs [ 4 ].

The disease associated with BHV-1 is an OIE-listed B disease and may show several clinical manifestations, including inflammatory reactions in both respiratory (Infectious Bovine Rhinotracheitis) and genital tracts (infectious pustular vulvovaginitis/balanoposthitis), conjunctivitis, encephalitis, abortion, infertility, mastitis, enteritis, and dermatitis. Also, the systemic form of the infection affecting visceral organs may develop in newborn calves [ 5 - 7 ]. When the disease occurs in unvaccinated dairy cattle, the incidence of the morbidity and case-fatality rates is 8% and 3%, respectively, but morbidity and mortality are higher in feedlot cattle [ 8 ].

The infection is mainly transmitted via nasal exudate and coughed-up droplets, ocular and genital secretions, fresh or frozen semen, as well as contaminated equipment and fetal fluids and tissues [ 9 , 10 ].

The BHV-1 virus is able to establish lifelong latency after a primary infection with a field isolate or vaccination with a weakened strain, and stressful conditions such as transportation, parturition, and glucocorticoid therapy may lead to reactivation and shedding of the virus, complicating control and eradication strategies [ 11 , 12 ].

In Iran, BHV-1 was for the first time reported between 1964 and 1968 based on clinical observations and serology [ 13 ]. In 1973-1975 BHV-1 was isolated from nasal secretions of imported cows with acute respiratory disease [ 14 ]. Since then, BHV-1 infection has been reported from several provinces and union territories of the country. As reports are available from different provinces at different time periods, unified data on the status of BHV-1 infection in Iran are missing. To address this critical knowledge gap, a systematic review and meta-analysis was conducted to determine the seroprevalence of BHV-1 infection in the cattle population of Iran and also to give useful outputs in formulating infection-control strategies.

2. Data Acquisition

2.1. Database search

For gathering information, articles regarding seroprevalence of bovine herpesvirus type 1 in apparently healthy cattle in Iran based on antibody-capture enzyme linked immono sorbert assay (ELISA) tests in both English and Farsi languages were searched in nine databases. These included: Five English databases (PubMed, Google Scholar, ScienceDirect, Web of Science, and Scopus) and four Persian databases (Magiran, Irandoc, and the Scientifc Information Database [SID]) for the articles published prior to November 2023. We also checked dissertations and all abstract books of scientific conferences in Iran from 2000 to 2023. In order to avoid missing any articles, the citations of the included articles were reviewed to seek out other relevant studies. The searched terms were: “Bovine herpesvirus type 1”, “cow”, “cattle”, “bovine”, “Iran”, “epidemiology”, and “prevalence” alone or combined with “OR” and/or “AND”.

2.2. Data collection

Figure 1 shows the items used for the meta‐analysis study (preferred reporting items for systematic reviews and meta-analyses extension for scoping reviews PRISMA]) process. After screening the titles and abstracts of articles identified by the initial search, those that describe the seroprevalence of BHV-1 by antibody-capture ELISA in apparently healthy cattle (cattle of all ages, irrespective of their breed) in Iran were considered for the study. Studies with other purposes, such as those with other animal species as target populations, those evaluating the molecular characteristics of the isolated virus, and studies detecting the virus or antibody in milk, semen, or aborted fetuses, were excluded. In the next step, for quality assessment of eligible studies, the strengthening the reporting of observational studies in epidemiology (STROBE) checklist was used. For each study, the following data were extracted: First author’s name, publication date, location of study, sample size, number of positive, study type, herd type, age of samples, and BHV-1 vaccination. Then the studies were grouped based on the animal level, i.e. individual and herd (Table 1).

Figure 1. PRISMA (preferred reporting items for systematic reviews and meta-analyses) flow diagram illustrating the selection process of included and excluded records

Study Area Herds (p/s) Animals (p/s) Herd Type (Sampling Age [m]), BoHV-1 Vaccination Study Design Ref.
West Azerbaijan 18/22 65/190 NA Retrospective [ 15 ]
Kurdistan - 169/454 NA Cross-sectional [ 16 ]
Khuzestan - 180/572 NA Cross-sectional [ 17 ]
Khorasan Razavi - 89/150 Dairy (>24) Cross-sectional [ 18 ]
Kerman 5/15 55/181 Dairy (12-36), No Cross-sectional [ 19 ]
Fars 39/39 237/856 Dairy (>12), No Cross-sectional [ 20 ]
Isfahan - 462/642 Dairy (>0), No Cross-sectional [ 21 ]
Fars - 20/56 NA Cross-sectional [ 22 ]
Khuzestan - 28/50 NA Cross-sectional [ 22 ]
Kohgilooye va Boyer Ahmad - 12/29 NA Cross-sectional [ 22 ]
Different regionsa 13/15 314/558 Dairy, beef (12-48), No Cross-sectional [ 23 ]
Markazi 11/12 286/803 Dairy (>12), No Cross-sectional [ 24 ]
Qazvin 5/8 36/504 Dairy (12-48), No Cross-sectional [ 25 ]
Hamedan 34/41 289/492 Dairy (>6), No Cross-sectional [ 26 ]
Chaharmahal va Bakhtiari - 103/192 Dairy Cross-sectional [ 27 ]
Khorasan - 88/290 Dairy Cross-sectional [ 27 ]
Semnan - 72/306 Dairy Cross-sectional [ 27 ]
Sistan and Baluchestan - 35/94 Dairy Cross-sectional [ 27 ]
Fars - 182/184 NA Cross-sectional [ 28 ]
Khuzestan - 260/534 (>0), No Cross-sectional [ 29 ]
Zanjan 8/10 64/562 (>0), No Cross-sectional [ 30 ]
Isfahan 16/16 156/216 Dairy (>12), No Cross-sectional [ 31 ]
Fars 13/18 167/420 Dairy (>0), No Cross-sectional [ 32 ]
Qazvin 9/16 52/1017 Dairy (>12), No Cross-sectional [ 33 ]
Yazd, South Khorasan 50/76 400/800 Dairy (>12), No Cross-sectional [ 34 ]
NA: Not available.
p/s: Number of positive samples/total sample
aProvinces of Yazd, Khorasan, Fars, Markazi, East Azerbaijan, and Qom.
Table 1.Documents included in the meta-analysis of the seroprevalence of BHV-1 in the cattle population of Iran

2.3. Statistical analysis

We estimated the pooled seroprevalence of Bovine herpesvirus type 1 in cattle using either the fixed-effects or random-effects model with a 95% confidence interval (CI) and a significant level of 5%, and the results are displayed using a forest plot accumulation chart. Heterogeneity among the included studies was assessed using Cochran’s heterogeneity statistic (Q-test) and I2 statistic. Egger’s regression test was used to evaluate possible publication bias. The analysis was done using Comprehensive Meta-Analysis software, version 3.

3. Results

As presented in Figure 1, initially, a total of 124 documents were collected. In secondary screening, based on title and abstract, 41 duplications were removed and 83 remained for full-text review. Of those, 34 documents were excluded based on title and abstract, and 29 documents were excluded based on the selection criteria. Finally, a total of 25 studies from 20 documents were eligible to be included in this meta-analysis study (Table 1). Based on our analysis, evidence of publication bias was not observed (P=0.295) (Figure 2).

Figure 2. Funnel plot to assess publication bias

The provinces where seroprevalence of BHV-1 among cattle in Iran was studied, are shown in Figure 3. The total seroprevalence of BHV-1 in apparently healthy cattle at the animal level, based on an antibody-capture ELISA test, was reported in 25 studies. Our study included a total of 10,151 cattle, and the overall prevalence of BHV-1, based on the random-effects model (I2=98.2, Q test P=0.00), was 40.2% (95% CI, 32.3%, 48.6%) (Figure 4). Also, the total prevalence of BHV-1 infection at the herd level was reported in 12 studies and 288 herds, and the overall prevalence, based on the random-effects model (I2=61.56, Q test P=0.00), was 75.5% (95% CI, 63.9%, 84.2%) (Figure 5).

Figure 3. Provinces where the seroprevalence of BHV-1 among cattle in Iran was studied

Figure 4. Forest plot for the seroprevalence of BoHV-1 in the cattle population at the animal level in Iran

Figure 5. Forest plot for the seroprevalence of BoHV-1 in the cattle population at the herd level in Iran

4. Discussion

According to the report by the Iranian Ministry of Agriculture (2018), there are approximately 8,000,000 cattle of three groups of cattle breeds in Iran, including pure exotic, crossbred native and exotic breeds, and pure native breeds that are kept in industrial, semi-industrial, and traditional husbandry systems. The most important breed is the Holstein, with an estimated annual milk and meat production of approximately 1,059,000 and 830 (×1000 tons), respectively.

From 1964-70 to date, BHV-1 antibody has been detected in cattle, sheep, goats, buffalo, camel, pig, and horse, and was isolated from cattle in Iran [ 13 , 35 ]. So far, a number of studies have been carried out on cattle in various parts of Iran (Table 1). To our knowledge, this is the first meta-analysis of the prevalence of BHV-1 infection in apparently healthy cattle based on the ELISA test in Iran.

There are differences between the reports of the seroprevalence rate from various countries and areas. Probably, this result might be associated with weather conditions, geographical situation, sample size, sampling season, diagnostic methods, diversity of breeds, age and sex, and husbandry systems. It is reported that colder and higher altitude areas can act as a risk factor for cattle herds experiencing BHV-1 infections [ 36 ]. It is well known that all breeds of cattle at any age are susceptible to BHV-1 infections; however, the disease is prevalent in older animals, probably because of their greater exposure to natural sources of infection and the loss of maternal immunity [ 8 ].

In light of our outcomes, the seroprevalence of BHV-1 among cows and herds was 40.2% (95% CI, 32.3%, 48.6%) and 75.5% (95% CI, 63.9%, 84.2%), respectively, in Iran. The pooled prevalence of BHV-1 was higher than that reported in a previous study carried out on 9968 sera collected from the whole country using the serum neutralization test, in which the rate of infection was estimated at 30.6% [ 37 ]. This shows that the situation of BHV-1 infection in Iran has become more serious in recent years.

There are many serologic reports on the cattle population from around the world. Based on a review of the epidemiology and control of BHV-1 infection in Europe [ 6 ], the serologic prevalence has been reported in cows as low as 12% in Scotland to as high as 77.5% in the Southern Italian Apennines, and in herds as low as 22% in Estonia to as high as 100% in Central Italy. The pooled estimate of seroprevalence of BHV-1 at the animal and herd level in Iran, in comparison with other countries, shows that Iran could be considered among the moderately infected countries.

BHV-1 infection can cause major economic consequences in cattle breeding herds, including abortion, infertility, loss of production, and deaths. The costs of treatment, prevention, and control measures should also be taken into account [ 38 ]. The most prevalent reason for culling cows in Iran is frequent abortion and reproductive failure [ 39 ]. Occurrence of highly prevalent abortion in the cattle population of Iran (11.1-18.6%) has multifactorial etiologies [ 40 ]. However, some researchers [ 41 - 44 ] believe that BoHV-1 can act as an abortion pathogen in cattle, as BoHV-1 DNA was isolated in 6.8-100% of aborted fetuses in different regions of Iran.

The control and eventual eradication of BoHV-1 is based on the detection and removal of infected animals, with or without the use of marker vaccines, but this approach is inefficient for the eradication of infection in countries with large herds or high seroprevalence of BHV-1. Alternatively, repeated vaccination of infected herds can be undertaken to increase protection, reduce the effects of disease, and reduce the risk of re-excretion by latently infected animals [ 26 , 45 ].

5. Conclusion

In conclusion, the endemicity of BHV-1 infection in the cattle population of Iran, with the high prevalence in herds and animals found in this study, suggests the necessity of an intensive control program for reducing BHV-1 infection rates. Based on the present findings, there are no national IBR/IPV control programs in Iran. A well-defined control strategy for preventing and controlling BHV-1 infection in Iran should be based on further studies on BHV-1 epidemiology, control of animal and semen importation, the use of marker vaccines, and planned biosecurity measures to control the epidemiological risk of infection due to the presence of BHV-1 latent carriers.

Acknowledgements

The authors would like to thank all the authors of the research papers included in this literature review.

Compliance with ethical guidelines

This article is a review study with no human or animal sample.

Data availability

The data that support the findings of this study are available upon request from the corresponding author.

Funding

This research did not receive any grant from funding agencies in the public, commercial, or non-profit sectors.

Authors' contributions

All authors contributed equally to the conception and design of the study, data collection and analysis, interception of the results and drafting of the manuscript. Each author approved the final version of the manuscript for submission.

Conflict of interest

The authors declared no conflict of interest.

References

  1. Levings RL, Roth JA. Immunity to bovine herpesvirus 1: I. Viral lifecycle and innate immunity. Anim Heal Res Rev. 2013; 14(1):88-102. DOI | PubMed
  2. Mahony TJ. Bovine herpesvirus: What is missing from our understanding of the relationship between BoHV-1 and BoHV-5? Vet J. 2010; 184(2):124-5. DOI | PubMed
  3. Hostnik P, Černe D, Mrkun J, Starič J, Toplak I. Review of Infections With Bovine Herpesvirus 1 in Slovenia. Front Vet Sci. 2021; 8:676549. DOI | PubMed
  4. Biswas S, Bandyopadhyay S, Dimri U, Patra PH. Bovine herpesvirus-1 (BHV-1) a re-emerging concern in livestock: A revisit to its biology, epidemiology, diagnosis, and prophylaxis. Vet Q. 2013; 33(2):68-81. DOI | PubMed
  5. Iscaro C, Cambiotti V, Petrini S, Feliziani F. Control programs for infectious bovine rhinotracheitis (IBR) in European countries: an overview. Anim Heal Res Rev. 2021; 22(2):136-46. DOI | PubMed
  6. Raaperi K, Orro T, Viltrop A. Epidemiology and control of bovine herpesvirus 1 infection in Europe. Vet J. 2014; 201(3):249-56. DOI | PubMed
  7. Newcomer BW, Cofield LG, Walz PH, Givens MD. Prevention of abortion in cattle following vaccination against bovine herpesvirus 1: A meta-analysis. Prev Vet Med. 2017; 138:1-8. DOI | PubMed
  8. Constable P, Hinchcliff KW, Done S, Walter G. A textbook of the diseases of cattle, horses, sheep, pigs, and goats. New York: Saunders Elsevier; 2017.
  9. Muylkens B, Thiry J, Kirten P, Schynts F, Thiry E. Bovine herpesvirus 1 infection and infectious bovine rhinotracheitis. Vet Res. 2007; 38(2):181-209. DOI | PubMed
  10. Mottaghian P, Raoofi A, Madadgar O, Badiei A, Ashrafi Tamai I. A Study on Mycoplasmal and Viral Infections in Bovine Keratoconjunctivitis. Iran J Vet Med. 2023; 17(4):345-52. DOI
  11. Levings RL, Roth JA. Immunity to bovine herpesvirus 1: II. Adaptive immunity and vaccinology. Anim Heal Res Rev. 2013; 14(1):103-23. DOI | PubMed
  12. Nandi S, Kumar M, Manohar M, Chauhan RS. Bovine herpes virus infections in cattle. Anim Heal Res Rev. 2009; 10(1):85-98. DOI | PubMed
  13. Derakhshan H. The presence of bovine herpes virus antibody in the serum of cows in Tehran province [DVM Thesis]. Tehran: Veterinary School of Tehran University, Iran; 1968.
  14. Hazrati A, Amjadi AR. The Isolation and Identification of Infectious Bovine Rhinotracheitis Virus in Iran. Arch Razi Inst. 1975; 27(1):21-35. https://archrazi.areeo.ac.ir/article_108772.html
  15. Morshedi A, Mahmoodian A, Dalir Naghadeh B. Detecting of anti BHV-l in milk and serum by ELISA, comparition using of milk and serum ELISA for deterine of BHV-l infection in cattle. J Vet Res. 2003; 58(3) https://jvr.ut.ac.ir/article_11915.html
  16. Rahmany F. Serological survay on Bovine Rhinotrchitis virus infection in Kudistan Province [DVM thesis]. Tehran: Veterinary School of Tehran University; 2004.
  17. Haji Hajikolaei MR, Seyfiabad Shapouri M. Seroepidemiological survey of infections with BHV-1 in Ahvaz cattle. Iran Vet J. 2006; 2(2):23-30.
  18. Hashemi Tabar GR, Rad M, Naseri Z, Azizzadeh M. Detection of antibody against infectious bovine rhinotracheitis glycoprotein gE in aborted cattle in Mashhad, Iran. Arch Razi Inst. 2009; 64(2):91-5. https://archrazi.areeo.ac.ir/article_103838.html
  19. Sakhaee E, Khalili M, Kazeminia S. Serological study of bovine viral respiratory diseases in dairy herds in Kerman province, Iran. Iran J Vet Res. 2009; 10(1):49-53. https://ijvr.shirazu.ac.ir/article_1089.html
  20. Badiei K, Ghane M, Mostaghni K. Seroprevalence of bovine herpes virus type 1 in the industrial dairy cattle herds in suburb of Shiraz-Iran. Aust J Basic Appl Sci. 2010; 4(10):4650-4. https://scholar.google.com/scholar?hl=en&as_sdt=0%2C5&q=Badiei+K%2C+Ghane+M%2C+Mostaghni+K.+Seroprevalence+of+bovine+herpes+virus+type+1+in+the+industrial+dairy+cattle+herds+in+suburb+of+shiraz-Iran.+Aust+J+Basic+Appl+Sci.+2010%3B+4%2810%29%3A4650-4.&btnG=
  21. Shirvani E, Lotfi M, Kamalzadeh M, Noaman V, Bahriari M, Morovati H, et al. Seroepidemiological study of bovine respiratory viruses (BRSV, BoHV-1, PI-3V, BVDV, and BAV- 3) in dairy cattle in central region of Iran (Esfahan province). Trop Anim Health Prod. 2012; 44(1):191-5. DOI | PubMed
  22. Namavari M, Hosseini M, Mansourian M, Shams Z, Amrabadi O, Tahamtan Y, et al. Testing for infective abortive agents in cattle in Iran. Online J Vet Res. 2012; 16(3):147-53. https://www.cabidigitallibrary.org/doi/full/10.5555/20123243072
  23. Sadri R. A new way of occurrence and serodiagnosis for Infectious Bovine Rhinotrchitis in Iranian cattle herds. Iran J Vet Med. 2012; 6(2):99-103. https://ijvm.ut.ac.ir/article_28954.html
  24. Ghaemmaghami S, Ahmadi M, Deniko A, Mokhberosafa L, Bakhshesh M. Serological study of BVDV and BHV-1 infections in industrial dairy herds of Arak, Iran. Iran J Vet Sci Technol. 2013; 5(2):53-61. https://ijvst.um.ac.ir/article_26986.html
  25. Ezzi A, Hatami A, Bakhshesh M, Shoukri MR, Gharaghozloyan M. Serological study of bovine herpesvirus type 1 and parainfluenza type 3 in cow farms of Qazvin province based on different ages and seasons. Arch Razi Inst. 2013; 68(1):53-7. https://archrazi.areeo.ac.ir/article_103912.html
  26. Bahari A, Gharekhani J, Zandieh M, Sadeghi-Nasab A, Akbarein H, Karimi-Makhsous A, et al. Serological study of bovine herpes virus type 1 in dairy herds of Hamedan province, Iran. Vet Res Forum. 2013; 4(2):111-4. http://vrf.iranjournals.ir/article_2675.html
  27. Nikbakht G, Tabatabaei S, Lotfollahzadeh S, Nayeri Fasaei B, Bahonar A, Khormali M. Seroprevalence of bovine viral diarrhoea virus, bovine herpesvirus 1 and bovine leukaemia virus in Iranian cattle and associations among studied agents. J Appl Anim Res. 2015; 43(1):22-5. DOI
  28. Kamkar-Salehi S, Namavari M. Study of using the triple Dot-ELISA for simultaneous diagnosis of Neospora caninum, IBR and BVDV. Vet Res Biol Prod. 2017; 30(4):134-40. https://vj.areeo.ac.ir/article_113200.html
  29. Adeli E, Pourmahdi Borujeni M, Haji Hajikolaei MR, Seifi Abad Shapouri MR. Bovine Herpesvirus-1 in Khouzestan province in Iran: Seroprevalence and risk factors. Iran J Ruminants Heal Res. 2017; 2(1):47-56. https://ijrhr.scu.ac.ir/article_14417.html
  30. Erfani AM, Bakhshesh M, Fallah MH, Hashemi M. Seroprevalence and risk factors associated with bovine viral diarrhea virus and bovine herpes virus-1 in Zanjan Province, Iran. Trop Anim Health Prod. 2019; 51(2):313-9. DOI | PubMed
  31. Noaman V, Nabinejad AR. Seroprevalence and risk factors assessment of the three main infectious agents associated with abortion in dairy cattle in Isfahan province, Iran. Trop Anim Health Prod. 2020; 52(4):2001-9. DOI | PubMed
  32. Hashemi M, Bakhshesh M, Manavian M. Bovine Viral Diarrhea Virus and Bovine Herpes Virus-1 in Dairy Cattle Herds in Fars Province, Southern Iran: Seroprevalence and Evaluation of Risk Factors. Arch Razi Inst. 2022; 77(5):1621-9. https://archrazi.areeo.ac.ir/article_126351.html
  33. Hashemi M, Bakhshesh M, Khezri M, Gharagouzlouian M, Tavakoli G. A two-year serological study of bovine viral diarrhea virus, bovine alphaherpesvirus 1 and bovine parainfluenza virus type 3 in Qazvin dairy cattle farms, Northwestern of Iran. Vet Arh. 2022; 92(1):1-10. DOI
  34. Karimi O, Bitaraf Sani M, Bakhshesh M, Zareh Harofteh J, Poormirzayee-Tafti H. Prevalence of bovine herpesvirus 1 antibodies and risk factors in dairy cattle of Iran’s central desert. Trop Anim Health Prod. 2022; 55(1):23. DOI | PubMed
  35. Afshar A, Tadjbakhsh H. Occurrence of precipitating antibodies to bovine herpes virus (infectious bovine rhinotracheitis) in sera of farm animals and man in Iran. J Comp Pathol. 1970; 80(2):307-10. DOI | PubMed
  36. Woodbine KA, Medley GF, Moore SJ, Ramirez-Villaescusa AM, Mason S, Green LE. A four year longitudinal sero-epidemiological study of bovine herpesvirus type-1 (BHV-1) in adult cattle in 107 unvaccinated herds in south west England. BMC Vet Res. 2009; 5:5. DOI | PubMed
  37. Kargar Moakhar R, Bokaie S, Akhavizadegan MA, Charkhkar S, Meshkot M. Seroepidemological Survey for Antibodies against Infectious Bovine Rhinotracheitis and Bovine Herpes 4 Viruses among Cattle in Different Provinces of Iran. Arch Razi Inst. 1989; 40(1):93-100. https://archrazi.areeo.ac.ir/article_109083.html
  38. Fernandes LG, Denwood MJ, de Sousa Américo Batista Santos C, Alves CJ, Pituco EM, de Campos Nogueira Romaldini AH, et al. Bayesian estimation of herd-level prevalence and risk factors associated with BoHV-1 infection in cattle herds in the State of Paraíba, Brazil. Prev Vet Med. 2019; 169:104705. DOI | PubMed
  39. Dirandeh E, Gholizadeh M, Kazemi Fard M, Javaheri H, Vahedi V, Khalilvandi H, et al. Reasons and timing of Holstein dairy cows culls during heat stress in Iran. Anim Sci J. 2016; 29(110):159-66. https://asj.areeo.ac.ir/article_106529.html
  40. Keshavarzi H, Sadeghi-Sefidmazgi A, Ghorbani G, Kowsar R. Phenotypic analysis of abortion incidence in Iranian Holstein cows. Iran J Anim Sci. 2016; 47(3):409-19. https://ijas.ut.ac.ir/article_59796.html
  41. Mahmoudinia M. Determination of bovine herpesvirus type 1(bhv1) in aborted fetuses in Khorasan Razavi Province by polymerase chain reaction [DVM thesis]. Mashhad: Veterinary School of Ferdowsi University; 2011.
  42. Merat E. Determining Contamination Frequency of Aborted fetuses of dairy cows in Moghan livestock breeding complex to BHV-1, BVDV, Leptospira Spp. and Neospora caninum by PCR methods [DVM thesis]. Tabriz: Veterinary School of Islamic Azad University, Tabriz, Iran; 2016.
  43. Sasani F, Vazirian A, Javanbakht J, Hassan MA. Detection of infectious bovine rhinotracheitis in natural cases of bovine abortion by PCR and histopathology assays. Am J Clin Exp Med. 2013; 1(2):35-9. DOI
  44. Kaveh AA, Merat E, Samani S, Danandeh R, Soltannezhad S. Infectious causes of bovine abortion in Qazvin province, Iran. Arch Razi Inst. 2017; 72(4):225-30. https://archrazi.areeo.ac.ir/article_113299.html
  45. Nettleton P, Russell G. Update on infectious bovine rhinotracheitis. In Pract. 2017; 39(6):255-72. DOI