Guidance

Investigating poor reproductive performance in cattle and sheep during Bluetongue outbreaks (accessible version)

Published 12 February 2026

Background

This document is intended to provide guidance on investigating poor reproductive performance in sheep flocks and cattle herds, during periods where bluetongue virus (BTV) should be considered as a potential cause. Poor reproductive performance may be characterised by all or one of lower-than-expected scanning or pregnancy diagnosis rates, infertility abortion or stillbirth.

There is a statutory requirement to report all bovine abortion cases:

Suggested test protocols may vary depending on whether there is one clinical sign or a range of reproductive signs and, is not exhaustive or intended to be wholly inclusive. Guidance is intended to aid sampling and testing in combination with clinical judgement and consideration of the flock or herd history. Veterinary Investigation Officers (VIOs) at your local surveillance pathology centre are happy to discuss cases and advise on sampling and testing.

Since the incursion of bluetongue virus serotype 3 (BTV-3) to England in 2024, consideration of BTV as a cause of infertility, abortion, stillbirth, and/or dummy animals is recommended. Clinical suspicion of BTV may depend on seasonality, herd or flock history, or vaccination status.

Bluetongue testing

Bluetongue is a notifiable disease. Where there is clinical suspicion of BTV, this must be reported to APHA field services (please see above details for reporting).

Where there is no clinical suspicion of bluetongue infection, testing is possible on samples sent directly to the Pirbright Institute: Get bluetongue testing.

To comply with current legislation, material or samples known or suspected to be infected with BTV cannot currently be accepted to APHA Veterinary Investigation Centres (VICs) or laboratories for examination or testing. Please discuss alternative options with the VIC or laboratory.

For further information on bluetongue and testing, including what happens if a test is positive, refer to current official guidance or get official advice: Bluetongue: latest situation and Get bluetongue testing

Diagnostic investigation

Poor reproductive performance can be attributable to infectious and non-infectious causes. A comprehensive history is essential to guide investigation, and it is important to consider non-infectious causes at the start of the investigation

Non-infectious causes

Management factors


  • Mating mismanagement – inappropriate timing or protocol, ram to ewe ration, luteolytic drugs
  • Handling – during early or late pregnancy, lack of dystocia intervention

Environmental factors


  • Weather – heat, adverse conditions
  • Stress – dog worry, competition

Genetic factors


  • Chromosomal abnormalities – incompatible with life, congenital malformations
  • Reproductive abnormalities – freemartins, penile abnormalities

Nutritional factors


  • Malnutrition – inadequate protein, energy, trace elements, minerals
  • Plant associated – phytoestrogens, teratogens, toxicity

Infectious causes

Testing for infectious causes of poor reproductive performance is indicated in the absence of obvious non-infectious factors, or where there is evidence of dam or sire illness. Not all infectious causes of abortion will result in systemic illness of the dam or sire. Suggested aetiologies and appropriate tests are detailed in the ‘test protocol’ section (Page 6).

The history may help determine whether dam or sire infertility, or both, are likely to be involved. If it is possible that sire infertility is involved, an examination similar to that used at pre-breeding soundness examination (PBSE) of the sires is advised in addition to infectious disease testing. Specific test protocols are detailed in the next section.

Test protocols

Infectious causes of poor reproductive performance in cattle herds

Table 1: Infectious disease affecting bull fertility


Note: Excludes other factors affecting service, for example lameness. Causes of infertility may be transient and resolve by the time of testing. However, consider PBSE in the first instance to rule out long term fertility effects.

Condition Test Sample type Notes
Venereal disease for example, Campylobacter, Trichomonas Culture and/or microscopy Sheath washing Campylobacter testing requires a specific sampling kit subject to additional cost. Contact the sales desk and request RAI 0800 on 03000 600001.
Pyretic agents  for example IBR, SBV, Leptospira, BVD, BTV Serology and/or PCR testing Example: respiratory swab, EDTA blood, serum Tests and samples specific to suspected infectious agent. Consider vaccine status for serological tests. Paired serology is more useful, unless demonstrating absence of exposure.
Samples for BTV testing sent to the Pirbright Institute.
Balanoposthitis  for example IBP, or secondary infection to injury Serology and/or PCR testing, bacteriology, microscopy EDTA blood, serum, semen None
Orchitis for example Trueperella, Histophilus Bacteriology, microscopy Semen Report clinical suspicion of brucellosis to APHA field services

Clinical suspicion of BTV infection must be reported to APHA.

Table 2: Infectious disease affecting cow fertility


Note: APHA must be notified of abortions or premature calvings within 24 hours: Brucella testing guidance. If foetal material is available, comprehensive testing of the calf is recommended (see table 3) in addition to statutory Brucella testing where applicable. Where there is suspicion of systemic disease in the dam or several reproductive signs, sampling of 5-6 affected dams is recommended.

Pathogen Test Sample type Notes
Schmallenberg virus ELISA serology Serum, milk Positive serology indicates previous exposure but does not indicate timing of exposure. Testing of yearlings as sentinel animals indicates exposure within the last breeding season.
Bovine Viral Diarrhoea PCR and/or ELISA serology Serum, milk If significant seroprevalence, consider a PI hunt.
Infectious bovine rhinotracheitis PCR and/or ELISA serology Nasopharyngeal or ocular swab, BAL fluid, serum, milk Consider vaccination history and requirement for gE-deleted ELISA testing.
Leptospira Serology Serum, milk MAT and ELISA for L. hardjo may be useful as IgM may have fallen by time of abortion.
Salmonella Culture and/or serology Faeces, swabs, serum None
Bluetongue PCR and ELISA serology EDTA blood and serum Samples sent to the Pirbright Institute.

Clinical suspicion of BTV infection must be reported to APHA.

Table 3: Testing of aborted or stillborn calves


Note: Comprehensive sampling is recommended where postmortem material is available. Brain cavitation should be reported as suspected BTV infection before considering other causative agents.

All tests listed below are from the APHA bovine abortion package TC0015. This package can be applied to whole fetuses submitted to a VIC or to samples submitted from on-farm investigations.

Sample Test Cause of abortion
Placenta including multiple cotyledons and intercotyledonary membrane Gross examination for placentitis and stained smear Coxiella burnetii (Q fever) and Brucella
Foetal stomach contents collected aseptically ideally using a vacutainer through the stomach wall Bacteriology Bacterial causes including Campylobacter and Salmonella
Spleen (Fresh) PCR BVD
Liver (Fresh) Additional bacteriology Bacterial causes including Campylobacter
Brain (Fresh) PCR SBV, Neospora caninum
Maternal blood – clotted MAT Leptospira hardjo
Maternal blood – clotted ELISA Neospora caninum, BVD, IBR

Table 4: Testing of brain cavitation and dummy calves


Note: Consider reporting suspicion of in utero Bluetongue virus infection in the first instance. Other congenital diseases can cause brain cavitation for example BVD or porencephaly of Limousin calves.

Pathogen Test Sample type Notes
Bluetongue PCR and ELISA serology EDTA blood and serum, spleen Consider with weak or ‘dummy’ calves. Samples sent to the Pirbright Institute.
Schmallenberg virus PCR and/or ELISA serology Brain, foetal fluid, serum If typical cases of arthrogryposis are PCR negative, consider calf/dam serology.
Bovine viral diarrhoea PCR and/or ELISA serology Spleen, serum Avoid antigen ELISA in calves <30 days old
Inherited disorder Histopathology and possible genetic analysis Fixed brain plus ear tissue Consider the breeding history

Clinical suspicion of BTV infection must be reported to APHA.

Infectious causes of poor reproductive performance in sheep flocks

Table 5: Infectious disease affecting tup fertility


Note: Exclude other factors affecting service, for example, lameness. Causes of infertility may be transient and resolve by the time of testing, however, consider breeding soundness testing in the first instance to rule out long term fertility effects.

Condition Test Sample type Notes
Balanoposthitis for example pizzle rot, orf, secondary infection to injury Bacteriology, electron microscopy Swab, skin crust/scab None
Orchitis, for example Corynebacterium, Trueperella Clinical examination, bacteriology Semen Report clinical suspicion of brucellosis to APHA field services
Pyretic agents for example  Mycoplasma, Pasteurellaceae, TBF, BTV PCR and ELISA serology EDTA blood and serum Samples for BTV testing sent to the Pirbright Institute

Clinical suspicion of BTV infection must be reported to APHA.

Table 6: Infectious disease affecting ewe fertility


Note: If abortion and/or stillbirth are the main sign with no dam illness, comprehensive testing of the lamb(s) is recommended (see table 7). Where there is suspicion of infectious disease, dummy lambs, or several reproductive signs, sampling of 5-6 affected dams is recommended.

Pathogen Test Sample type Notes
Schmallenberg virus ELISA serology Serum Positive serology indicates previous exposure but cannot determine timing of exposure in adults; testing of yearlings as sentinel animals indicates exposure within the last year.
Border Disease PCR and/or ELISA serology Serum If significant seroprevalence consider a PI hunt.
Toxoplasmosis ELISA or LAT serology Serum Consider vaccination status. Negative maternal serology can be used to rule out exposure.
Subacute fluke Egg detection in faeces or coproantigen ELISA Faeces Other clinical signs may include loss of condition and anaemia.
Tickborne fever PCR EDTA blood None
Bluetongue PCR and ELISA serology EDTA blood and serum Samples sent to the Pirbright Institute.
Iceberg diseases for example MV, Johne’s PCR and/or ELISA serology EDTA blood and serum None

Clinical suspicion of BTV infection must be reported to APHA.

Table 7: Testing of aborted or stillborn lambs


Note: Comprehensive sampling is recommended where postmortem material is available. Brain cavitation should be reported as suspected BTV infection before considering other causative agents.

All tests listed below are from the APHA small ruminant abortion packages TC0011 (fetuses +/- placenta from one dam) and TC0012 (fetuses +/- placentae from two dams). These packages can be applied to whole fetuses submitted to a VIC or to samples submitted from on-farm investigations.

Sample Test Cause of abortion
Placenta including multiple cotyledons and intercotyledonary membrane Gross examination for placentitis and stained smear Chlamydia (EAE), Coxiella (Q fever) and Brucella
Foetal stomach contents collected aseptically ideally using a vacutainer through the stomach wall PCR Toxoplasma gondii
Foetal stomach contents collected aseptically via a syringe and needle or with a vacutainer Bacteriology Bacterial causes including Campylobacter species and Salmonella
Spleen (Fresh) PCR Border disease
Liver (Fresh) Additional Bacteriology Bacterial causes including Campylobacter species
Brain (Fresh) PCR SBV
Maternal blood – clotted Ab ELISA Chlamydia abortus
Maternal blood – clotted LAT Toxoplasma gondii
Maternal blood – clotted Ab ELISA, PCR Border disease

Table 8: Testing of brain cavitation and dummy lambs


Note: Suspicion of in utero Bluetongue virus infection must be reported to APHA in the first instance.

Pathogen Test Sample type Notes
Bluetongue PCR and ELISA serology EDTA blood and serum, spleen Consider with weak or ‘dummy’ lambs.
Samples sent to the Pirbright Institute.
Schmallenberg virus PCR and/or ELISA serology Brain, foetal fluid, serum If typical cases of arthrogryposis are PCR negative, consider lamb/dam serology.
Border disease virus PCR and/or ELISA serology Spleen, serum None

Clinical suspicion of BTV infection must be reported to APHA.

  1. Investigating Poor Scanning Rates in Sheep Flocks (Scotland’s Rural College)
  2. APHA guidance on sample and test selection
  3. Official Veterinarian Training
  4. Bluetongue: how to spot and report it
  5. Bluetongue: how to spot and report the disease (GOV.SCOT)
  6. Bluetongue virus (GOV.WALES)