Transmissible Diseases in Sperm Donation: Viruses, Bacteria and Genetic Risks

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Written by Zappelphilipp Marx13 June 2025
Laboratory technician analysing a semen sample

In India, each year thousands of people turn to sperm donation to realise their dream of starting a family. Modern screening methods significantly reduce health risks, yet a small residual risk remains. This article outlines which viruses, bacteria, parasites and inherited disorders can be transmitted—and how multi-stage laboratory screenings minimise those risks.

Why Multi-Stage Screening Is Essential

Pathogens often go through a window period: they’re present in donor samples but not yet detectable by antibody tests alone. The Indian Council of Medical Research (ICMR) and the Indian Society for Assisted Reproduction (ISAR) recommend combining serological assays with PCR testing and quarantining donor samples for several months before release.

Viruses Detectable in Ejaculate

  • HIV – ELISA and PCR testing, plus sample quarantine.
  • Hepatitis B & C – antibody and antigen assays to prevent liver damage.
  • Herpes Simplex Virus 1 & 2 – PCR testing; low risk in asymptomatic donors.
  • Cytomegalovirus (CMV) – IgG/IgM screening; critical for immunocompromised recipients.
  • Zika Virus – RT-PCR and antibody testing after travel to endemic areas.
  • HTLV I/II – rare but associated with leukaemia.
  • Human Papillomavirus (HPV) – PCR for high-risk types (cervical cancer prevention).
  • West Nile & Dengue Viruses – important for donors from tropical or subtropical regions.
  • SARS-CoV-2 – included in some screening panels during peak pandemic periods.

Bacteria and Parasites in Semen

  • Chlamydia trachomatis – often asymptomatic; can impair fertility.
  • Neisseria gonorrhoeae – detected via NAAT or culture swabs.
  • Treponema pallidum (Syphilis) – mandatory TPPA and VDRL serology.
  • Urogenital Flora such as E. coli and enterococci – can cause inflammation.
  • Trichomonas vaginalis – known to reduce sperm quality.
  • Mycoplasma/Ureaplasma – often silent, yet inflammatory.

Genetic Risk Factors

  • Cystic Fibrosis – CFTR gene analysis
  • Tay-Sachs Disease – HEXA mutation screening
  • Spinal Muscular Atrophy – SMN1 gene testing
  • Sickle Cell & Thalassaemia – haemoglobinopathy panels
  • Fragile X Syndrome – FMR1 gene repeat analysis
  • Y-Chromosome Microdeletions – linked to severe oligospermia
  • Gaucher Disease – relevant for Ashkenazi Jewish donors
  • Population-Specific Panels – e.g. Fanconi anaemia, Wilson’s disease

Which Diseases Can Be Ruled Out?

By combining serology, PCR, genetic panels and a multi-month quarantine, laboratories can effectively exclude all relevant viruses, bacteria, parasites and inherited disorders—driving the residual risk to an exceptionally low level.

The Screening Process

  1. Health History – comprehensive questionnaire and counselling.
  2. Laboratory Tests – antibody, antigen and PCR assays.
  3. Genetic Panel – screening for common hereditary conditions.
  4. Quarantine – samples stored frozen for at least three months.
  5. Retest – confirm absence of new infections before release.

Private Donation vs. Sperm Bank

Accredited sperm banks in India ensure maximum safety with regulated testing, quarantine protocols and donor registries. Private donations can offer a more personal approach and may be more economical, but they require bespoke testing arrangements and legal agreements.

RattleStork app home screen
Figure: RattleStork – the sperm donation apps

Conclusion

Sperm donation opens the door to parenthood for many. A thorough, ICMR- and ISAR-recommended screening protocol is essential to virtually eliminate the risk of infection or genetic disorder transmission. Trust accredited clinics or vetted platforms—and give your future family the safest possible start.

Frequently Asked Questions (FAQ)

With combined PCR and antibody testing, a three-month quarantine and final retesting, the residual risk is under 0.1 %.

Standard panels cover HIV, Hepatitis B/C, Syphilis, Chlamydia, Gonorrhoea, CMV, HTLV, HPV plus a genetic screening panel.

Yes. Samples are screened immediately and again after the quarantine period using ELISA and PCR.

Absolutely. HBsAg, anti-HBc and anti-HCV assays are required by regulation.

A urine or urethral swab tested by NAAT confirms absence of Chlamydia.

Common screenings include Cystic Fibrosis, SMA, Sickle Cell/Thalassaemia, Fragile X and population-specific panels.

To bridge the window period for many pathogens; a second blood test is done before release.

In India, total costs including screening typically range from ₹50,000 to ₹80,000 per sample.

Donors are usually aged 18–40, in good health, STI-negative and meet strict sperm quality standards.

No. Only accredited sperm banks follow standardised testing, quarantine and legal safeguards.

The child has a legal right to learn the donor’s identity once they reach adulthood.

PCR swabs for high-risk HPV types; positive samples are discarded.

Zika can persist in semen for months and cause foetal defects; RT-PCR rules out this risk.

Yes. Many centres only accept CMV-negative donors to minimise complications.

Consultation → Consent → Blood & Urine Tests → Donation → Quarantine → Retest → Release → Insemination.

Clinical pregnancy rates are about 15–20 % per insemination; over three cycles, cumulative rates exceed 50 %.

Yes. Any positive cultures undergo antibiotic sensitivity testing; resistant strains are excluded.

Stored in liquid nitrogen (–196 °C), semen can remain viable for decades.

Many fertility centres treat recipients up to age 45; beyond that, health risks increase significantly.

Absolutely. High sperm count and motility greatly improve fertilisation chances and are verified before release.