Abstract
Abortion is a major issue in sheep husbandry. It can result in significant economic losses and a severe public health risk. This survey assessed the infectious and non-infectious causes of abortion in Iranian sheep flocks and determined the main risk factors. In this cross-sectional survey, causes of abortion were evaluated in 757 sheep flocks, and risk factors were analysed. A checklist containing general animal information for each abortion outbreak evaluated was filled in. Data were analysed using univariate tests and multivariable binary logistic regression analysis. In this sense, parity, gestational age of the aborted fetus, vaccination protocol, mineral supplementation and history of stillbirth showed significant associations with abortion. Infectious agents such as Coxiella burnetti (22.7%), Chlamydia abortus (12.3%) and Brucella melitensis (10.4%) were the most frequently isolated in the investigated flocks, with more than 2% of abortion rates. On the other hand, non-infectious agents such as trauma, pregnancy toxaemia and vitamin E/Se deficiency were involved in those flocks with low abortion rates (less than 10%). Results revealed multiple causes of abortion outbreaks among Iranian sheep flocks, which need careful investigation to identify possible aetiology and risk factors. Further studies are necessary to evaluate if these factors are similar to other countries in the same region.
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Introduction
Small ruminants have a significant role in the Iranian agricultural economy and perform as leading actors in the field of the livelihoods of nomadic and rural farmers (Esmaeili and Hamedi 2018). Iran has more than 30 indigenous breeds of sheep with a population of 45 million heads (Ministry of agriculture 2020). The primary purpose of the Iranian breeds is meat production, which leads to an annual production of 265,000 tons (Ministry of agriculture 2020). Mutton meat is essential in food self-sufficiency and supplies a sound animal protein source. Milk is also a vital product for Iranian sheep, producing 252,000 tons/year, providing for a large part of the population (Ministry of agriculture 2020). Due to these reasons, sheep abortions severely affect food production, animal health and the agricultural economy. In addition, its zoonotic potential can pose a serious risk to public health.
According to Iran Veterinary Organization (IVO) protocols, Iranian sheep health plans include vaccination against brucellosis, sheep pox, Peste des Petits Ruminants (PPR), anthrax, Foot-and-mouth disease (FMD), contagious agalactia and enterotoxemia. However, the last two are not mandatory (Esmaeili et al. 2017).
Abortions can result in significant economic losses and severe risks to public health. Financial losses are associated with both direct and indirect costs. Some of these indirect costs are related to an increase in lambing intervals, which supposes more food expenses, a detriment in the incomes of sold muttons, fewer replacement lambs available and an increase in veterinary treatments (Pugh and Baird 2012).
In most sheep flocks, the percentage of ewes visibly aborting is less than 2% (Menzies 2011), being this considered a normal rate. Therefore, in the present study, an abortion outbreak was considered when the total percentage of abortions exceeded 2%.
There are various potential agents underlying the causes of abortion, which can mainly be classified into infectious and non-infectious. Non-infectious causes remain unknown in most abortions because they do not produce a high percentage of aborted ewes and therefore are not studied in depth. Infectious causes, which are more rapidly diagnosed, are more critical (Njaa 2011). However, several non-infectious aetiologies can be associated with abortions in sheep, such as traumatism, pregnancy toxaemia, vitamin E/Se deficiency, stressful handling, overcrowding, or even consuming toxic plants (Youngquist and Threlfall 2006; Pugh and Baird 2012). Non-infectious causes are usually related to a low rate of abortion. However, infectious aetiology is mainly associated with severe abortion outbreaks with relevant human health implications (Noakes et al. 2018). In sheep, the major infectious causes of abortion are bacteriological agents, such as Campylobacter spp, Brucella melitensis, Listeria spp, Salmonella spp, Coxiella burnetii, and Chlamydia abortus (Youngquist and Threlfall 2006; Pugh and Baird 2012). Furthermore, other infectious causes of viral origin include Border disease virus, Bluetongue and Schmallenberg virus. Likewise, parasites such as Toxoplasma gondii or Neospora caninum are common pathogens implicated in fetal losses (Youngquist and Threlfall 2006; Pugh and Baird 2012).
Significant differences exist in the prevalence of different infectious agents in other countries. Thus, in research conducted in England by the Veterinary Investigation Diagnosis Analysis (VIDA) between 2011 and 2018, bacteriological agents were the leading cause of abortion, being C. abortus (45%) the most frequently isolated agent (Carson 2018). In general, repeated surveys carried out in Europe have indicated C. abortus as a significant abortifacient agent in small ruminants (Navarro et al. 2009), although other pathogens can emerge occasionally. In southern European countries, as well as in many Asian and African regions, B. melitensis is also a significant pathogen in small ruminant farms (Lacasta et al. 2015). In contrast, in New Zealand, Campylobacter spp. and Salmonella brandenburg are the primary microbial abortifacient agents, whilst C. abortus and C. burnetii infections have never been diagnosed in that country (West 2002). Likewise, Campylobacter spp. is a significant cause of small ruminant abortion also in North America (Hazlett et al. 2013).
In Iran, an abortion research survey conducted by Hamedi et al. in 2020 found that 23.5% of abortions in sheep and goats were caused by C. abortus (Hamedi et al. 2020). Another survey performed in southern Iran detected C. abortus, C. burnetii and Mycoplasma agalactiae as the main abortion agents in aborted fetuses (Heidari et al. 2018). In Ethiopia, Gebretensay et al. (2019), reported that up to 20% of sheep flocks had recent abortion outbreaks, obtaining 89.0% of seropositive results for Chlamydia spp., 68.3% for C. burnetti and 70.8% for T. gondii (Gebretensay et al. 2019).
The reproductive performance should be improved in sheep flocks in order to increase the production of lamb and other products. Thus, identifying the causes of abortion and their risk factors is crucial. The present survey aimed to identify the most common causes of sheep abortion and its risk factors in Iranian sheep flocks.
Materials and methods
Design and case selection
From 2015 to 2019, a cross-sectional survey was performed on 757 sheep flocks in Iran. The sheep breeds included in the research were local breeds such as Ghezel, Afshar, Zandi, Shall, Lori, Arabi, Torki-Ghashghaei, Bakhtiyari, Sanjabi, Moghani, Zel, Sangsari and Naeini.
During the lambing season, flocks were under active surveillance for abortion, and all flocks in this survey were visited and examined by a veterinarian. The percentage of abortions was calculated based on the number of pregnant ewes, and each flock was sampled once. After compiling the clinical history provided by the farmer, the aborted ewes were examined by the veterinarian and the collected samples were sent to the laboratory with ice (-20ºC). There, the fetuses were necropsied and sampled.
General information about each flock and affected animals was recorded (Table 2). Each item was dichotomised to either zero (for no) or one (for yes). Since the abortion rate of less than 2% is normal in sheep flocks, these flocks were considered control.
A case was defined as one or more fetuses or tissues submitted to a microbiology laboratory simultaneously from a single flock. Cases consisting of intact fetuses or tissues from necropsies conducted in the field only were included if all the following fresh tissues were available for evaluation: brain, heart, lung, liver, kidneys and abomasal contents. Abortion work-ups included evaluation of clinical history and necropsy findings. Gestational age was estimated using crown-rump length measurements at the time of necropsy (Noden and Lahunta, 1985).
Sampling
Before collecting blood, the sheep's wool was trimmed around the jugular region. Blood sampling consisted of collecting aseptically 2 ml of blood by jugular venepuncture, with the collected volume divided equally between a sterile blood collection tube (to obtain the serum for BHB analysis) and a second tube containing ethylenediaminetetraacetic acid (EDTA) anticoagulant (for PCR analysis of BTV). Blood and separated serum were stored at − 20 °C until processing.
Blood samples were taken only from ewes with clinical signs of pregnancy toxaemia (hind limbs oedema or thin ewes that aborted twins) and those with blue tongue symptoms (bloody discharge from the nose and mouth, swelling and oedema of the lips and gums, swollen and purple tongue). Stomach content, brain, heart and lung of aborted fetuses were taken aseptically for culture and molecular detection of infectious agents.
Bacteriological culture
The samples of aborted fetuses were inoculated on Blood agar and MacConkey agar (Merck, Germany) in order to isolate bacteria that were cultivable on routine media cultures. A pair of plates were incubated aerobically, and the other pair anaerobically for 48 h at 37 °C. The plates were inspected for bacterial growth after 16–20 h of cultivation and after an additional 24 h in cases of no or slow bacterial growth at first inspection. The selection of colonies for subculturing was based on colony morphology and the number of colony types that were not considered post-mortem contamination. Colonies were subcultured and identified using standard methods for phenotypical characterisation (Koneman et al. 1997).
"Other bacteria" were defined as agents other than Campylobacter spp., Salmonella spp., C. abortus, Mycoplasma spp. B.melitensis, Trueperella pyogenes, Listeria monocytogenes, E. coli or C. burnetii. Mixed cultures containing fewer than three distinct bacterial colony types with no confirmed pathogenic bacteria were not considered positive for an etiologic agent.
Mycologic examination
A sterile disposable syringe was used to aseptically collect l-3 ml of abomasal content to diagnose mycotic infections. In addition, portions of the lung, eyelid, and skin (if there was evidence of dermatitis) were collected depending on the availability of fetal tissues. A sterile scalpel was used to scrape a small amount of material from any fetal skin with gross lesions. This material, fetal lung that had been macerated with a sterile mortar and pestle, and 0.2 ml of fetal abomasal content were separately spread onto the surface of plates of Sabouraud dextrose agar (SDA) containing 1,000 units/ml of penicillin G. Solid media were incubated at both room temperature, and 37° C. Plates were examined daily for the first week and twice each week for the next two weeks. Portions of detectable mycotic growth were transferred to potato dextrose agar (PDA) and SDA plates and slants. PDA was used as a growth medium for slide cultures, incubated for 3–7 days and then stained with lactophenol cotton blue. Filamentous isolates were identified from gross and microscopic characteristics (Beneke and Rogers. 1971). Fungal diagnoses included visualising disseminated hyphal elements or yeast with or without positive cultures from nonplacental sites (to remove bias from possible environmental contamination).
Molecular analysis
According to the manufacturers' instructions, DNA/ RNA was extracted from 25 mg of tissue samples using a DNA/RNA extraction kit (High Pure PCR Template Preparation Kit, Roche Company, Germany), and diagnosis of each abortion agent was performed using the PCR assays as described previously in the literature: Mycoplasma spp. (Van Kuppeveld et al., 1992), Trueperella pyogenes (Ülbegi-Mohyla et al., 2010), Border disease (Vilček and Paton, 2000), Bluetongue (Anthony et al., 2007), Campylobacter spp. (Bang et al., 2001), Toxoplasma gondii (Burg et al., 1989), Brucella melitensis (Bricker and Halling, 1994), Listeria monocytogenes (Gouws and Liedemann, 2005), Coxiella burnetii (Hoover et al., 1992), Salmonella spp. (Rahn et al., 1992), Chlamydia abortus (Laroucau et al., 2001).
Pregnancy toxaemia
Beta-hydroxy butyrate was measured in serum samples using the Williamson-Mellanby enzymatic method (Commercial kit, Biorex Fars Company, Shiraz, Iran) and animals that showed a BHB concentration greater than three mmol/l were considered suffering from pregnancy toxaemia (Radostits and Gay 2017).
Final diagnosis
The final diagnosis was based on characteristic gross changes detected at necropsy and the diagnostic test results. Criteria for trauma included full-term lambs with head haemorrhage, rib fractures, intrathoracic haemorrhage, and/or ruptured liver, with no detection of infectious agents in any examined tissues. Vitamin E/selenium deficiency was diagnosed following the method described by Liu et al. (Liu et al., 1996). Finally, congenital defects were determined by fetus examination.
Statistical analysis
The data were analysed using IBM.SPSS 25 (SPSS Inc., Chicago, IL, USA). Categorical data were presented as frequency (percentage). Univariate analysis of categorical data was conducted using the chi-square test. In univariate analyses, a multivariate binary logistic regression model included the significant variables at p values below 0.2. The results were presented as odds ratio (OR) and 95% confidence interval (CI). P values below 0.05 were considered statistically significant. Sheep flocks with a < 2% abortion rate were considered control and compared with those flocks with more than 2% abortion rate.
Results
Over the 757 studied flocks, two hundred and thirteen (213/757: 28.1%) had an abortion rate below 2%, which, following the literature (Menzies 2011), was considered normal in a sheep flock. The remaining 544 flocks (544/757: 71.8%) had pathological abortion rates (> 2%). The final cause of the abortion was determined in 301 of the 544 abortion outbreaks analysed (55.3%).
As shown in Table 1, infectious agents were diagnosed as a cause of abortion in 287 flocks (287/757: 37.9%). Infectious agents were isolated in 2.8% (6/213) of the flocks with an abortion rate lower than 2% and 51.6% (281/544) of the flocks with an abortion rate higher than 2%. The leading infectious agent diagnosed in the survey was Chlamydia abortus which was diagnosed in 67 outbreaks (67/544: 12.3%), followed by Brucella melitensis (57/544: 10.4%), Coxiella burnetti (26/544: 4.8%), Salmonella spp. (24/544: 4.4%), Campylobacter spp. (20/544: 3.7%) Mycoplasma spp. (13/544: 2.4%), Escherichia coli (11/544: 2%), Bluetongue virus (10/544: 1.9%), Fungi. (11/757: 1.5%), Aspergillus fumigatus (8/544: 1.5%), Candida albicans (3/544: 0.6%) and Listeria spp. (7/544: 1.3%).
Attending to the classification of the causative agent, bacteriological agents caused abortion in 255 flocks (255/544: 46.9%), while viral agents affected 14 flocks (14/544: 2.6%), and fungal agents were diagnosed in 8 flocks (8/544: 1.5%).
Non-infectious causes such as trauma (10/757:1.3%), pregnancy toxaemia (9/757:1.2%), and Vitamin E/selenium deficiency (7/757:0.9%) were mainly identified in flocks with a low abortion rate, being diagnosed in 26 studied flocks (26/757: 3.4%).
In univariate analyses, birth, flock type, gestational age of the aborted fetus, history of Rev-1 vaccination, routine visit of veterinarian, vaccination protocol according to IVO, mineral supplementation and history of stillbirth had significant associations with abortion at p < 0.05 (Table 2). According to Multivariable binary logistic regression analysis, sheep that have not been vaccinated according to IVO protocols were at higher risk of suffering abortion than the others (OR: 0.04; 95% CI: 0.00–0.34; P = 0.009) (Table 2).
Discussion
This investigation is the first extensive epidemiological survey of the leading causes of abortion in Iranian sheep flocks. It provides insights into abortion agents and the risk factors involved. The causes of abortion depending on the percentage of abortion rate and the role of infectious and non-infectious causes in these reproductive failures are illustrated.
It was possible to determine the final cause of abortion in 55.3% of the studied cases with more than 2% of animals aborted. However, the success in diagnosing augmented as the abortion rate increased due to the more significant enrolment of the infectious agents in abortion outbreaks. Thus, in those flocks with an abortion rate higher than 30%, the final diagnosis was reached in more than 85% of the cases. In agreement with our results, in a study carried out in Canada, abortion agents were diagnosed in 90 out of 163 sheep fetuses (55%) and 66 of 96 goat fetuses (69%) (Hazlett et al. 2013). Likewise, in the Netherlands, infectious agents were detected in 48% of the ovine submissions (Van den Brom et al. 2012). A failure to diagnose an abortive process may be due to other different causes such as genetic, metabolic, hormonal, developmental disorders, or other reasons, which are often difficult or impractical to confirm in a routine diagnostic procedure. However, many fetuses for which no aetiology is detected have an infectious cause (Anderson 2007).
The risk of transmission of infectious agents in Iran is high due to the traditional rearing of lambs. There is a traditional trade of lambs younger than three weeks of age during the lambing season in Iran. These lambs, coming from different flocks, are reared together, fattened, and prepared for slaughter. Likewise, the ewes are slaughtered after lambing for meat production, and the lambs are sold to other flocks and reared by goats or ewes whose lambs had died or were aborted. Due to the higher adult weight of sheep and better carcass production than goats, some farmers sell their kids and rear orphaned lambs by does. Some other farmers buy these orphaned lambs to stimulate milk production of aborted ewes or to be raised by ewes whose lambs have died. Therefore, many lambs and kids from flocks with different health statuses are sold and distributed among other flocks, and the possibility of spreading various infectious agents increases (Esmaeili and Hamedi 2018).
In the present survey, various infectious agents of sheep abortion were identified, and in 46.9% of the cases, bacteria were the leading causes. According to reports from Veterinary Investigation Diagnosis Analysis of Britain from 2011 to 2018, the bacteria had the highest percentage among other infectious abortive agents (Carson 2018). In the present investigation, C.abortus, B.melitensis and C.burnetti were responsible for a high number of abortion outbreaks, especially with abortion rates higher than 10%. C. abortus has been reported as the predominant abortifacient bacterium throughout the world. Various reports from different countries showed the involvement of this bacterium in abortion storms and flocks with endemic abortion problems (OIE 2018).
Furthermore, a high prevalence of C. abortus (24.1%) among small ruminant flocks was previously reported in Iran (Esmaeili et al. 2015). Likewise, in previous studies developed in Iran, B. melitensis, Campylobacter spp., C.abortus, T.gondii, and Salmonella spp. were the leading causes of abortion recorded in small ruminant flocks (Behzadi Shahrbabak 2019). Similarly, another survey performed in southern Iran showed that Brucella spp., Salmonella spp., Campylobacter spp. and E.coli were isolated in 20.5%, 19.6%, 7.5%, and 26.1% aborted fetuses in conventional culture, respectively (Firouzi 2006). Campylobacter spp. was isolated in 3.7% of the abortion outbreaks in our survey. In this sense, 9.1% and 1.5% of sheep fetuses in the Tabriz region in Iran were positive for C. fetus subsp. fetus and C. jejuni using PCR (Fallah et al. 2014).
Q fever has been reported among livestock and human populations in Iran and has a high seroprevalence. It has also been detected in milk, and aborted fetuses and seroprevalence among sheep flocks was reported 24.7% (Mobarez et al.2017). Mycoplasma spp. was detected in 1.7% of aborted fetuses in the present research, well below the 30.8% isolated from Sistan and Baluchestan province, southeastern Iran (Hosein Abadi et al. 2019). A survey was performed in 2017 on 70 sheep flocks that suspected contagious agalactia from 10 provinces of Iran (Shamsaddini Bafti et al. 2017). The results showed that 36% of the animals had Mycoplasma infection. However, only 6% of them were related to M. agalactiae. Because mycoplasmas other than M. agalactiae can also cause abortion, the M. agalactiae vaccine may not be totally effective (Hosein Abadi et al. 2019). Differences found among the results of abortion agents in mentioned studies might be due to the diagnostic techniques used, methods and times of sampling, infection rate, different control strategies of each country such as vaccines, use of antibiotics, farmer training, quality of available vaccines and breeding type.
Toxoplasma infection was found in aborted fetuses in this survey. The overall seroprevalence rate of this infection among Iranian sheep was estimated to be 31%, and the infection rate in sheep over 1-year-old was 2.4 times more than in younger ones (Sharif et al. 2015). Numerous studies indicate high seroprevalence of Toxoplasma infection among sheep in Iran (Hamzavi et al. 2007; Asgari et al. 2013), France (Dumètre et al. 2006), and Turkey (Yildiz et al. 2014). In contrast, other studies that have identified T. gondii as an abortion agent have reported low rates (Razmi et al. 2010; Rassouli et al. 2011; Habibi et al. 2012).
Most surveys in the world have not evaluated the viral causes of abortion in small ruminant flocks except for some, which have reported a variety of results (Behzadi Shahrbabak 2019; Alemayehu et al. 2021). Border disease is considered endemic in small ruminants in Iran, and our results showed that 0.5% of fetuses were infected with the BDV. In the research of Kaleibar et al. (2014), carried out in Iran, which was conducted among suspected ewes with a history of reproductive failure, 11.3% were positive for the genome of the Border virus. Likewise, limited virological studies have been performed to determine the sheep abortion due to BDV. According to Mokhtari and Manshoori, 9% of aborted fetuses were positive for BDV using the RT-PCR test in Iran (Mokhtari and Manshoori. 2018). However, Hemmatzadeh et al. did not report any positive cases of BDV in free-ranging wild ruminants of Iran (Hemmatzadeh et al. 2016). According to our findings, 1.9% of aborted fetuses were infected with the Bluetongue virus (BTV). Different serological studies have been performed to detect BTV antibodies among sheep in Iran and other countries, showing different rates of seroprevalence (Lundervold et al. 2003; Ravishankar et al. 2005; Gür. 2008; Khezri and Azimi 2013; Abera et al. 2018; Elmahi et al. 2020). Cattle infected with BVDV and BTV can infect sheep, and in rural areas of Iran and other countries where pregnant sheep and cattle are reared in close contact, this can be an important source of infection transmission (Radostits and Gay 2017).
This survey identified infectious agents such as E. coli and other bacteria in low abortion rate flocks. When bacteria not generally related to ovine abortion were isolated in pure culture from fetal tissues, the isolated microbe was considered the abortion agent. These factors mainly cause sporadic abortions (Hassani-Tabatabaei and Firouzi 2005). Previous research indicates that endotoxins released from gram-negative bacteria such as E.coli and Salmonella can cause abortion due to prostaglandins release (Schlafer et al. 1994; Youngquist and Threlfall 2006). On the other hand, E.coli and other bacteria involved in sporadic abortions can likely be considered opportunists (Kirkbride 1993). In a survey performed in the Netherlands, 5% of sheep abortions among 98 ovine fetuses were reported due to E. coli (Van Engelen et al. 2014). Hay and silage storage are not well done in traditional rearing systems; consequently, feeding mouldy hay or poor-quality silage to pregnant ewes increases the risk of abortion due to mycotoxins and fungi (Radostits and Gay 2017).
Non-infectious agents rarely cause an abortion rate higher than 2% in the flock, and in abortion outbreaks with higher rates, an infectious agent is likely the cause (Noakes et al. 2018). Our findings revealed that in flocks with less than 2% abortion, only 2.8% of cases were caused by infectious agents. In addition, congenital defects, pregnancy toxaemia, trauma, and Vit E/selenium deficiency were 0.4%, 1.2%, 1.3% and 0.9% of flock abortion causes, respectively. Unlike goats, pregnancy toxaemia is not common among indigenous Iranian ewes for two reasons: First, their litter size is 1 to 1.2, and secondly, they have fat tails, and they can metabolise this fat storage in an energy crisis, reducing the risk of pregnancy toxaemia. Nevertheless, most regions in Iran are generally Se deficient (Mohri et al. 2011), and despite the direct effect of vitamin E as an antioxidant being obvious (McDowell et al. 1996), some reports on the impact of vitamin E on lamb survival are vague. According to the research of Dønnema et al., there was no effect on the stillbirth rate for ewes having ≤ 2 lambs (Dønnem et al. 2015). Other researchers also found no effect in lamb mortality when supplementing vitamin E in the last weeks of pregnancy (Merrell 1998; Daniels et al. 2000). A survey of abortion factors in Switzerland did not report Vitamin E/Selenium deficiency in aborted sheep fetuses, and in their report, only 2% of aborted kids were for this reason (Chanton-Greutmann et al. 2002).
A substantial number of fetuses in flocks with less than a 10% of abortion rate were undiagnosed in our survey. Unbalanced feed, environmental, hormonal and toxic stressors can affect the ability of the pregnant animals to sustain their fetus and frequently results in no identifiable abortion agents (Clothier and Anderson. 2016). Due to a lack of references on fetal concentrations of minerals, confirmation of mineral imbalances is severely limited, whereas toxic agents responsible for abortion may not be present once tissues are examined (Anderson 2007). Enhanced diagnostic methods for non-infectious agents would increase the likelihood of obtaining a definite result in such cases.
According to multivariate binary logistic regression analysis, the gestational age of aborted fetuses was related to abortion. The majority of aborted fetuses were > 3 months when fetal demands on the ewe are most significant. This is due to two main reasons: Firstly, the primary abortion agents cause abortions during late pregnancy. Secondly, early abortions do not attract the attention of the farmers. Then, since ewes are still in the breeding season, they return to estrus and may become pregnant again (Hamedi et al. 2020; Esmaeili et al. 2021). Likewise, this survey revealed a significant correlation between abortion and lack of mineral supplementation in animal feed. Mineral supplementation can enhance the health condition of animals and is necessary to stimulate an immune response (Suttle 2010). Similar research indicated a significant correlation between C. abortus infection and mineral supplementation in small ruminant flocks of Iran (Esmaeili et al. 2021). Further, mineral supplementation helps prevent or reduce the incidence of abortion in sheep (Aytekin and Aypak 2011). Contrary to our findings, some other reports mentioned no relationship between mineral/concentrate supplementation and abortion in sheep flocks (Hidiroglou 1979; Pond and Wallace 1986; Naziroğlu et al. 1998).
This survey revealed that farmers who vaccinated their flocks according to the IVO's schedule had fewer abortion rates. It should be noted that this is not only because of vaccines but also because of better rearing management in these flocks. Among the various infectious causes obtained in this survey, only brucellosis and contagious agalactia commercial vaccines are available in Iran.
The history of Rev-1 vaccination against B. melitensis did not show a relationship with abortion in multivariate binary logistic regression analysis. Vaccination with Full dose (FD) Rev-1 at 3 to 8 months of age confers an immunity that lasts 2.5 years in sheep (Radostits and Gay 2017). FD Rev-1 vaccine has been used in Iranian flocks since 1963, and from 2003 to 2013, a reduced dose (RD) Rev-1 was included in the national control program for adult sheep (Esmaeili et al. 2012b). Since the RD Rev-1 vaccine was removed from the control program, the immunity duration of FD Rev-1 is shorter than the reproductive life of ewes (Esmaeili et al. 2012a). Therefore, there are still abortions due to brucellosis in sheep flocks of Iran.
Analyzing multivariable logistic regression, the history of stillbirth is a risk factor for abortion in Iranian sheep flocks. Since most infectious causes of abortion can also cause stillbirth (Youngquist and Threlfall 2006), the presence of stillbirth is expected in these flocks. In accordance with our results, the history of stillbirths in the flock was recognised as an abortion risk factor in previous investigations (Dechicha et al. 2020; Esmaeili et al. 2021).
Various studies have evaluated the risk factors for the most relevant abortion agents in sheep flocks and reported a variety of results. In line with our results, they showed no significant association between abortion and flock size, type of farming, grazing system and contact with other flocks (Kardjadj et al. 2016). In contrast to our results, another study suggests a significant association between abortion and flock size, but their flock size differed (< 15 and > 30) (Gebretensay et al. 2019). Our results demonstrate that the presence of cattle and dogs was not identified as a risk factor for abortion, as was reported in other studies in Algeria and Ethiopia (Gebremedhin et al. 2013; Dechicha et al. 2020).
In conclusion, the results obtained in the present survey revealed that multiple agents are involved in abortion among Iranian sheep flocks (Table 2). The use of vaccines in the control of reproductive diseases of sheep is an essential part of any flock health program and one of the main requirements in intensive systems. Given that most sheep farming in Iran is traditional, any abortion control plan is doomed to failure regardless of the farmers' training.
Data availability
The data supporting this study's findings are available from the corresponding author upon reasonable request.
References
Abera T, Bitew M, Gebre D, Mamo Y, Deneke Y, Nandi S (2018) Bluetongue disease in small ruminants in south western Ethiopia: Cross-sectional sero-epidemiological study. BMC Res Notes 11:1–6
Agriculture Ministry (2020) Annual report of farm animal products in Iran. ministry of agriculture. Aitken, I., Diseases of sheep. John Wiley & Sons
Alemayehu G, Mamo G, Alemu B, Desta H, Tadesse B, Benti T, Bahiru A, Yimana M, Wieland B (2021) Causes and flock level risk factors of sheep and goat abortion in three agroecology zones in Ethiopia. Fron Vet Sci 8:27
Anderson ML (2007) Infectious causes of bovine abortion during mid-to late-gestation. Theriogenology 68:474–486
Anthony S, Jones H, Darpel KE, Elliott H, Maan S, Samuel A, Mellor P, Mertens PPC (2007) A duplex RT-PCR assay for detection of genome segment 7 (VP7 gene) from 24 BTV serotypes. J Virol Methods 141:188–197
Asgari Q, Sarkari B, Amerinia M, Panahi S, Mohammadpour I, Sarvestani AS (2013) Toxoplasma Infection in farm animals: A seroepidemiological survey in Fars province, south of Iran. Jundishapur J Microbiol 6:269–272
Aytekin I, Aypak SU (2011) Levels of selected minerals, nitric oxide, and vitamins in aborted Sakis sheep raised under semitropical conditions. Trop Anim Health Prod 43:511–514
Bang DD, Pedersen K, Madsen M (2001) Development of a PCR assay suitable for Campylobacter spp. mass screening programs in broiler production. J Rapid Meth Aut Mic 9:97–113
Behzadi Shahrbabak MJ (2019) A review on infectious agents of sheep and goats abortion in Iran. New Find Vet Microbiol 1:102–113
Beneke ES, Rogers AL (1971) Medical mycology manual. Medical mycology manual
Bricker BJ, Halling SM (1994) Differentiation of Brucella abortus bv. 1, 2, and 4, Brucella melitensis, Brucella ovis, and Brucella suis bv. 1 by PCR. J Clin Microbiol 32:2660–2666
Burg JL, Grover CM, Pouletty P, Boothroyd JC (1989) Direct and sensitive detection of a pathogenic protozoan, Toxoplasma gondii, by polymerase chain reaction. J Clin Microbiol 27:1787–1792
Carson A (2018) Abortion in sheep: an update. Vet Rec 183:528–529
Chanton-Greutmann H, Thoma R, Corboz L, Borel N, Pospischil A (2002) Abortion in small ruminants in Switzerland: investigations during two lambing seasons (1996–1998) with special regard to chlamydial abortions. Schweiz Arch Tierheilkd 144:483–492
Clothier K, Anderson M (2016) Evaluation of bovine abortion cases and tissue suitability for identification of infectious agents in California diagnostic laboratory cases from 2007 to 2012. Theriogenology 85:933–938
Daniels J, Hatfield P, Burgess D, Kottt R, Bowman J (2000) Evaluation of ewe and lamb immune response when ewes were supplemented with vitamin E. J Anim Sci 78:2731–2736
Dechicha AS, Moula N, Gharbi I, Baazize-ammi D, Akloul K, Guetarni D (2020) Abortions in cattle and sheep herds in algeria, descriptive study and risk factors. Agricultura 113(1–2)
Dønnem I, Randby Å, Hektoen L, Avdem F, Meling S, Våge Å, Ådnøy T, Steinheim G, Waage S (2015) Effect of vitamin E supplementation to ewes in late pregnancy on the rate of stillborn lambs. Small Rumin Res 125:154–162
Dumètre A, Ajzenberg D, Rozette L, Mercier A, Dardé ML (2006) Toxoplasma gondii infection in sheep from Haute-Vienne, France: seroprevalence and isolate genotyping by microsatellite analysis. Vet Parasitol 142:376–379
Elmahi MM, Karrar ARE, Elhassan AM, Hussien MO, Enan KA, Mansour MA, El Hussein ARM (2020) Serological Investigations of Bluetongue Virus (BTV) among Sheep and Goats in Kassala State, Eastern Sudan. Vet Med Int 20:1–7
Esmaeili H, Bolourchi M, Mokhber-Dezfouli MR (2015) Seroprevalence of Chlamydia abortus infection in sheep and goats in Iran. Iranian J Vet Med 9:73–77
Esmaeili H, Bolourchi M, Mokhber-Dezfouli MR, Teimourpour A (2021) Detection of Chlamydia abortus and risk factors for infection in small ruminants in Iran. Small Rumin Res 197:106339. https://doi.org/10.1016/j.smallrumres.2021.106339
Esmaeili H, Garavand M, Hamedi M, Mombeini M (2017) Evaluation of national anthrax strategy in livestock in Iran. J Vet Res 72:277–282
Esmaeili H, Hamedi M (2018) Color atlas of sheep and goat diseases of Iran. Tehran University Press
Esmaeili H, Partovi R, Marhamati Khamemeh B, Hamedi M, Khaji L (2012a) Evaluation of the national sheep and goat brucellosis control program in Iran. J Arak Univ Med Sci 14:9–20
Esmaeili H, Tajik P, Ekhtiyarzadeh H, Bolourchi M, Hamedi M, Khalaj M, Amiri K (2012b) Control and eradication program for bovine brucellosis in Iran: an epidemiological survey. J Vet Res 67:211–221
Fallah S, Hamali H, Jafari Joozani R, Zare P, Norsaadat G (2014) A molecular (PCR) survey on abortions caused by Campylobacter spp. in sheep flocks located on the suburb of Tabriz. Iran J Vet Sci Tech 6:23–29
Firouzi R (2006) Bacteriological study of abortion in ewes of Shiraz area. J Vet Res 61:15–17
Gebremedhin EZ, Agonafir A, Tessema TS, Tilahun G, Medhin G, Vitale M, Di Marco V (2013) Some risk factors for reproductive failures and contribution of Toxoplasma gondii infection in sheep and goats of Central Ethiopia: a cross-sectional study. Res Vet Sci 95:894–900
Gebretensay A, Alemayehu G, Rekik M, Alemu B, Haile A, Rischkowsky B, Aklilu F, Wieland B (2019) Risk factors for reproductive disorders and major infectious causes of abortion in sheep in the highlands of Ethiopia. Small Rumin Res 177:1–9
Gouws PA, Liedemann I (2005) Evaluation of diagnostic PCR for the detection of Listeria monocytogenes in food products. Food Technol Biotechnol 43:201–205
Gür S (2008) A serologic investigation of blue tongue virus (BTV) in cattle, sheep and gazella subgutturosa subgutturosa in southeastern Turkey. Trop Anim Health Prod 40:217–221
Habibi G, Imani A, Gholami M, Hablolvarid M, Behroozikhah A, Lotfi M, Kamalzade M, Najjar E, Esmaeil-Nia K, Bozorgi S (2012) Detection and identification of Toxoplasma gondii type one infection in sheep aborted fetuses in Qazvin Province of Iran. Iran J Parasitol 7:64
Hamedi M, Esmaeili H, Madani SA, Tajik P (2020) The Frequency of Abortion Caused by Chlamydia abortus in Aborted Fetuses of Sheep and Goats in Iran. J Med Bacteriol 9:1–8
Hamzavi Y, Mostafaie A, Nomanpour B (2007) Serological prevalence of toxoplasmosis in meat producing animals. Iran J Parasitol 7–11.
Hassani-Tabatabaei AM, Firouzi R (2005) Animal diseases due to bacteria, 2nd edn. University of Tehran press, Tehran
Hazlett MJ, McDowall R, DeLay J, Stalker M, McEwen B, van Dreumel T, Spinato M, Binnington B, Slavic D, Carman S (2013) A prospective study of sheep and goat abortion using real-time polymerase chain reaction and cut point estimation shows Coxiella burnetii and Chlamydophila abortus infection concurrently with other major pathogens. J Vet Diagn Invest 25:359–368
Heidari S, Derakhshandeh A, Firouzi R, Ansari-Lari M, Masoudian M, Eraghi V (2018) Molecular detection of Chlamydophila abortus, Coxiella burnetii, and Mycoplasma agalactiae in small ruminants’ aborted fetuses in southern Iran. Trop Anim Health Prod 50:779–785
Hemmatzadeh F, BoardmanW AA, Hematzade A, Moghadam MK (2016) Molecular and serological survey of selected viruses in free-ranging wild ruminants in Iran. PLoS ONE 11:e0168756
Hidiroglou M (1979) Trace element deficiencies and fertility in ruminants: a review. J Dairy Sci 62:1195–1206
Hoover T, Vodkin M, Williams J (1992) A Coxiella burnetti repeated DNA element resembling a bacterial insertion sequence. J Bacteriol 174:5540–5548
Hosein Abadi E, Saadati D, Najimi M, Hassanpour M (2019) A study on Mycoplasma agalactiae and Chlamydophila abortus in aborted ovine fetuses in Sistan and Baluchestan region. Iran Arch Razi Inst 74:295–301
Kaleibar MT, Madadgar O, Jalilvand A, Mohammadpour H (2014) A survey on the status of the border disease virus infection in sheep with reproductive failure using cell culture and polymerase chain reaction (PCR) methods in Tabriz. Iran Comp Clin Pathol 23:1429–1434
Kardjadj M, Kouidri B, Metref D, Luka PD, Ben-Mahdi MH (2016) Abortion and various associated risk factors in small ruminants in Algeria. Prev Vet Med 123:97–101
Khezri M, Azimi SM (2013) Seroprevalence of bluetongue disease in sheep in west and northwest provinces of Iran. Vet Res Forum 4:195–198
Kirkbride CA (1993) Diagnoses in 1,784 ovine abortions and stillbirths. J Vet Diagn Invest 5:398–402
Koneman EW, Allen SD, Janda W, Schreckenberger P, Winn W (1997) Diagnostic microbiology. The nonfermentative gram-negative bacilli. Lippincott-Raven Publishers, Philedelphia, pp 253–320
Lacasta D, Ferrer LM, Ramos JJ, González JM, Ortín A, Fthenakis GC (2015) Vaccination schedules in small ruminant farms. Vet Microbiol 181(1–2):34–46
Laroucau K, Souriau A, Rodolakis A (2001) Improved sensitivity of PCR for Chlamydophila using pmp genes. Vet Microbiol 82:155–164
Liu Q, Scheller K, Arp S, Schaefer D, Williams S (1996) Titration of fresh meat color stability and malondialdehyde development with Holstein steers fed vitamin E-supplemented diets. J Anim Sci 74:117–126
Lundervold M, Milner-Gulland E, O’callaghan C, Hamblin C (2003) First evidence of bluetongue virus in Kazakhstan. Vet Microbiol 92:281–287
McDowell L, Williams S, Hidiroglou N, Njeru C, Hill G, Ochoa L, Wilkinson N (1996) Vitamin E supplementation for the ruminant. Anim Feed Sci Tech 60:273–296
Menzies P (2011) Control of important causes of infectious abortion in sheep and goats. Veterinary Clinics: Food Anim Pract 27:81–93
Merrell B (1998) The effects on lamb survival rate of supplementing ewes with vitamin E during late pregnancy. Proceedings of meetings-sheep veterinary society. Sheep Veterinary Society Proceedings 22:57–61
Mobarez AM, Amiri FB, Esmaeili S (2017) Seroprevalence of Q fever among human and animal in Iran; A systematic review and meta-analysis. PLoS Negl Trop Dis 11:4
Mohri M, Ehsani A, Norouzian M, Bami MH, Seifi HA (2011) Parenteral selenium and vitamin E supplementation to lambs: hematology, serum biochemistry, performance, and relationship with other trace elements. Biol Trace Elem Res 139:308–316
Mokhtari A, Manshoori M (2018) Genomic identification of border disease virus in sheep aborted foetuses. Bulg J Vet Med 21:358–363
Navarro JA, Ortega N, Buendia AJ, Gallego MC, Martinez CM, Caro MR, Sanchez J, Salinas J (2009) Diagnosis of placental pathogens in small ruminants by immunohistochemistry and PCR on paraffin-embedded samples. Vet Rec 165:175–178
Naziroğlu M, Mehmet Ç, Karataş F, Çimtay İ, Aksakal M (1998) Plasma levels of Some Vitamins and Elements in Aborted Ewes in Elazığ Region. Turk J Vet Anim Sci 22:171–174
Njaa BL (2011) Kirkbride’s diagnosis of abortion and neonatal loss in animals. John Wiley & Sons
Noakes DE, Parkinson TJ, England GC (2018) Arthur's Veterinary Reproduction and Obstetrics-E-Book. Elsevier Health Sciences, Amsterdam
Noden DM, Lahunta Ad (1985) The embryology of domestic animals. Developmental mechanisms and malformations. Williams & Wilkins, Philadelphia
Pond W, Wallace M (1986) Effect of gestation-lactation diet calcium and zinc levels and of parenteral vitamins A, D and E during gestation on ewe body weight and on lamb weight and survival. J Anim Sci 63:1019–1025
Pugh DG, Baird NN (2012) Sheep & Goat medicine-E-book. Elsevier Health Sciences
Radostits O, Gay C (2017) A textbook of the diseases of cattle, horses, sheep, pigs and goats. Saunders Elsevier, Edinburgh
Rahn K, De Grandis S, Clarke R, McEwen S, Galan J, Ginocchio C, Curtiss Iii R, Gyles C (1992) Amplification of an invA gene sequence of Salmonella typhimurium by polymerase chain reaction as a specific method of detection of Salmonella. Mol Cell Prob 6:271–279
Rassouli M, Razmi G, Bassami M, Movassaghi A, Azizzadeh M (2011) Study on ovine abortion associated with Toxoplasma gondii in affected herds of Khorasan Razavi Province, Iran based on PCR detection of fetal brains and maternal serology. Parasitol 138:691
Ravishankar C, Nair GK, Mini M, Jayaprakasan V (2005) Seroprevalence of bluetongue virus antibodies in sheep and goats in Kerala State, India. Rev Sci Tech off Int Epizoot 24:953
Razmi GR, Ghezi K, Mahooti A, Naseri Z (2010) A serological study and subsequent isolation of Toxoplasma gondii from aborted ovine fetuses in Mashhad area. Iran J Parasitol 96:812–814
Schlafer D, Yuh B, Foley G, Elssaser T, Sadowsky D, Nathanielsz P (1994) Effect of Salmonella Endotoxin Administered to the Pregnant Sheep at 133–142 Days Gestation on Fetal Oxygenation, Maternal and Fetal Adrenocorticotropic Hormone and Cortisol, and Maternal Plasma Tufnor Necrosis Factor α Concentrations. Biol Reprod 50:1297–1302
Shamsaddini Bafti M, Pourbakhsh S, Ezatkhah M, Ashtari A (2017) Detection of Mycoplasma agalactiae in Small Ruminants of Southeast Iran. Arch Razi Inst 72:237–242
Sharif M, Sarvi S, Shokri A, Teshnizi SH, Rahimi M, Mizani A, Ahmadpour E, Daryani A (2015) Toxoplasma gondii infection among sheep and goats in Iran: a systematic review and meta-analysis. Parasitol Res 114:1–16
Suttle NF (2010) Mineral nutrition of livestock, 4th edn. Cabi, Cambridge
Ülbegi-Mohyla H, Hijazin M, Alber J, Lämmler C, Hassan A, Abdulmawjood A, Prenger-Berninghoff E, Weiss R, Zschöck M (2010) Identification of Arcanobacterium pyogenes isolated by post mortem examinations of a bearded dragon and a gecko by phenotypic and genotypic properties. J Vet Sci 11:265
Van den Brom R, Lievaart-Peterson K, Luttikholt S, Peperkamp K, Wouda W, Vellema P (2012) Abortion in small ruminants in the Netherlands between 2006 and 2011. Tijdschr Diergene 137:450–457
Van Engelen E, Luttikholt S, Peperkamp K, Vellema P, Van den Brom R (2014) Small ruminant abortions in The Netherlands during lambing season 2012–2013. Vet Rec 174:506
Van Kuppeveld F, Van der Logt J, Angulo A, Van Zoest M, Quint W, Niesters H, Galama J, Melchers W (1992) Genus-and species-specific identification of mycoplasmas by 16S rRNA amplification. Appl Environ Microbiol 58:2606–2615
Vilček Š, Paton DJ (2000) A RT-PCR assay for the rapid recognition of border disease virus. Vet Res 31:437–445
West D (2002) Ovine abortion in New Zealand. New Zeal Vet J 50:93–95
Yildiz K, Kul O, Gökpinar S, Atmaca HT, Gencay YE, Gazyağci AN, Babür C, Gürcan İS (2014) The relationship between seropositivity and tissue cysts in sheep naturally infected with Toxoplasma gondii. Turk J Vet Anim Sci 38:169–175
Youngquist RS, Threlfall WR (2006) Current therapy in large animal Theriogenology-E-Book. Elsevier Health Sciences, Amsterdam
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Hossein Esmaeili and Delia Lacasta conceived and designed the experiments; Amir Pasha Shakeri, Zia Nosrati Rad, and Ehsan Baghal Arani performed the sample collection; and laboratory examination; Hossein Esmaeili and Amir Pasha Shakeri analysed the data; Hossein esmaeili, Delia lacasta, Héctor Ruiz and Sergio Villanueva-Saz wrote the manuscript; Hossein esmaeili and Delia lacasta did the project management; Hossein esmaeili and Delia lacasta, Héctor Ruiz, Sergio Villanueva-Saz reviewed the manuscript and corrected the manuscript.
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Esmaeili, H., Shakeri, A.P., Rad, Z.N. et al. Causes of abortion in Iranian sheep flocks and associated risk factors. Vet Res Commun 46, 1227–1238 (2022). https://doi.org/10.1007/s11259-022-09986-5
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DOI: https://doi.org/10.1007/s11259-022-09986-5