What is the recommended microbiology screening for a transplant patient, including tests for viral and bacterial infections, such as Cytomegalovirus (CMV) and Methicillin-resistant Staphylococcus aureus (MRSA), and latent infections like Tuberculosis (TB)?

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Microbiology Screening for Transplant Candidates

All transplant candidates require comprehensive pre-transplant infectious disease screening to identify active infections requiring treatment, determine post-transplant prophylaxis strategies, and assess transplant eligibility. 1

Viral Screening Panel

Cytomegalovirus (CMV)

  • Both donor and recipient must be screened by CMV serology (IgG) prior to transplant 2
  • CMV serostatus determines risk stratification and prophylaxis strategy, with donor-positive/recipient-negative (D+/R-) representing the highest risk group 3, 4
  • No routine pre-transplant viral load monitoring is needed; quantitative PCR monitoring begins post-transplant 2

Epstein-Barr Virus (EBV)

  • Pre-transplant EBV serology (IgG) is essential for risk stratification 2, 5
  • EBV-seronegative recipients receiving organs from seropositive donors have increased risk of post-transplant lymphoproliferative disorder 5, 6
  • Screening helps guide post-transplant monitoring intensity 7, 5

Hepatitis B Virus (HBV)

  • Screen all candidates with HBsAg, anti-HBc (total), and anti-HBs (quantitative) 4
  • Anti-HBs ≥10 IU/mL indicates protective immunity from vaccination or resolved infection 4
  • Positive anti-HBc with negative HBsAg indicates prior exposure and may require prophylaxis depending on organ type 4

Hepatitis C Virus (HCV)

  • HCV antibody screening is mandatory for all transplant candidates 4
  • Positive antibody requires confirmatory HCV RNA testing to distinguish active from resolved infection 4
  • Active HCV infection does not contraindicate transplantation but requires post-transplant antiviral therapy planning 4

Human Immunodeficiency Virus (HIV)

  • HIV antigen/antibody combination screening is required for all candidates 4
  • HIV-positive status is no longer an absolute contraindication with modern antiretroviral therapy 4

Other Viral Pathogens

  • Consider screening for HSV and VZV serology to guide prophylaxis strategies 5, 6
  • Geographic-specific screening (e.g., West Nile virus, HTLV-1/2) based on epidemiologic risk 8, 6

Bacterial Screening

Methicillin-Resistant Staphylococcus aureus (MRSA)

  • No routine bacterial screening is recommended by transplant guidelines 2
  • However, MRSA nasal swab screening is commonly performed in clinical practice for decolonization protocols, particularly in lung and heart transplant candidates
  • Cultures should only be obtained when clinical symptoms suggest active infection 2

Active Bacterial Infections

  • Any suspected active bacterial infection requires appropriate cultures before transplantation 2
  • Active untreated bacterial infections typically require treatment completion before proceeding with transplant 1

Mycobacterial Screening

Tuberculosis (TB)

  • Screen all transplant candidates for latent TB infection 4, 1
  • Interferon-gamma release assay (IGRA) such as QuantiFERON-Gold is preferred over tuberculin skin testing in transplant candidates 4
  • Positive IGRA indicates latent TB requiring treatment before or after transplantation but does not contraindicate organ donation or receipt 4
  • Chest radiograph should be obtained in all candidates to exclude active TB 1

Fungal Screening

Endemic Mycoses

  • Screening for endemic fungi (Histoplasma, Coccidioides, Blastomyces) should be based on geographic exposure history 1, 5
  • Serologic testing or antigen detection may be indicated in high-risk populations 1

Candida and Aspergillus

  • No routine screening is recommended; surveillance cultures are not predictive of invasive disease 1

Parasitic Screening

Strongyloides

  • Screen candidates with epidemiologic risk factors (endemic area residence or travel) with Strongyloides serology 1
  • Untreated strongyloidiasis can cause fatal hyperinfection syndrome post-transplant 1

Toxoplasma

  • Toxoplasma serology (IgG) is particularly important for heart transplant candidates 1, 5
  • Seronegative recipients of seropositive donor hearts require prophylaxis 5

Trypanosoma cruzi (Chagas Disease)

  • Screen candidates with Latin American origin or exposure history 1

Critical Timing and Documentation

All screening should be completed during the pre-transplant evaluation period, ideally before listing 1. Results must be documented and readily available at the time of transplant to guide immediate post-transplant prophylaxis decisions 2.

Common Pitfalls to Avoid

  • Do not rely on historical serologies—repeat testing if previous results are more than 6-12 months old, as serostatus may change 1
  • Window period infections can be missed—antibody testing alone may not detect recent infections; consider nucleic acid testing for high-risk donors 4
  • False-negative results occur with hemodilution—ideally obtain samples before massive transfusions 4
  • A single positive coagulase-negative Staphylococcus blood culture without symptoms is typically a contaminant, not true bacteremia 2

References

Research

Recipient screening prior to solid-organ transplantation.

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2002

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

CMV Management Post Lung Transplant

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Interpretation of Infectious Disease Test Results for Organ Donation Eligibility

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Viral infection in renal transplant recipients.

TheScientificWorldJournal, 2012

Research

Viral infection after renal transplantation: surveillance and management.

Clinical journal of the American Society of Nephrology : CJASN, 2008

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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