Volume 26, Number 3—March 2020
Progressive Vaccinia Acquired through Zoonotic Transmission in a Patient with HIV/AIDS, Colombia
In March 2015, a patient in Colombia with HIV/AIDS was hospitalized for disseminated ulcers after milking cows that had vesicular lesions on their udders. Vaccinia virus was detected, and the case met criteria for progressive vaccinia acquired by zoonotic transmission. Adherence to an optimized antiretroviral regimen resulted in recovery.
Vaccinia virus (VACV) belongs to the genus Orthopoxvirus (OPXV) and was the main component of vaccines used during the 1960s and 1970s against smallpox (1). More recently, VACV has caused several zoonotic outbreaks in South America (2,3), where human cases are mainly associated with occupational exposure of farmworkers to infected cows. Progressive vaccinia is a severe and often lethal condition caused by infection and uncontrolled replication of VACV in immunocompromised patients (4,5).
In November 2014, a 30-year-old man with HIV/AIDS living and working at a rural dairy cattle farm in the department of Cundinamarca, Colombia, with no prior hospitalizations for opportunistic infections sought treatment for a suppurative ulcer with initial sharply raised defined edges on his right hand (Figure 1, panel A), right ear, and distal left leg that appeared 1 week after he had milked cows with similar lesions on their udders. He had recently interrupted antiretroviral therapy after onset of depression because of his father’s death 4 months before. Despite treatment with self-formulated antimicrobial drugs and home therapies (application of alcohol, methylene blue, and herbs), the lesions continued and spread within 1 month to his nostrils, glans penis, right leg, right knee, and ankles. On November 14, 2014, the patient was treated with antimicrobial drugs at a local hospital and instructed to comply with his antiretroviral therapy. On December 9, 2014, after failing to respond to treatment, the patient was referred to the Hospital Universitario Mayor Méderi in Bogotá, Colombia. Laboratory tests showed a CD4 cell count of 11 cells/mL and HIV viral load of 44,201 copies/mL. The patient was treated with acyclovir after suspected initial diagnosis of alphaherpesvirus infection and was discharged on December 23, 2014, with antimicrobial therapy prophylaxis for opportunistic infections (trimethoprim/sulfamethoxazole) and persuaded to continue his previous antiretroviral therapy (lamivudine/zidovudine and efavirenz).
The patient was readmitted to the hospital on March 24, 2015, because of a deteriorating clinical condition that included deep, severe, and extended foul-smelling ulcers with raised and undefined edges throughout his face and extremities (Figure 1, panels B and C), as well as fever, tachycardia, hearing and vision impairment, anemia, and leukopenia. He received a blood transfusion, prophylactic antimicrobial drugs against opportunistic infections, analgesics, and supportive care. The case was suggestive of poxvirus infection because the patient had not received smallpox vaccination, the pathologic study showed the presence of cytoplasmic B-type inclusion bodies, and the patient reported previous contact with cattle with vesicular lesions in their udders. Therefore, biological samples were remitted to the Instituto Nacional de Salud for viral diagnostics, and, subsequently, to the US Centers for Disease Control and Prevention for confirmation of VACV diagnosis and further characterization.
On March 30, 2015, HIV resistance to antiretroviral drugs was confirmed, and the pharmacologic therapy was changed to raltegravir and darunavir/ritonavir. Within 2 weeks, the lesions had healed considerably, and the patient was discharged from the hospital on April 20. Follow-up visits revealed complete healing of the lesions, mild scarring, and depigmentation (Figure 1, panel D), with the exception of a persistent ulcer on the patient’s left leg. This lesion did not respond to initial antimicrobial treatment or a 2-week course of topical imiquimod.
Experimental assays included ELISA and neutralization tests for OPXV IgM and IgG detection, virus isolation in BSC-40 cells, and molecular detection through OPXV-generic and VACV-specific real-time PCR (Appendix). OPXV IgM and IgG antibodies were detected in serum in March 2015 (5 months after illness onset). IgG but not IgM was in serum in July 2015 (9 months after illness onset). Viral neutralization assays had 50% effective concentration values of 1:517 for the March sample and 1:223 for the July sample (Table). VACV persisted in lesions despite the presence of OPXV IgM and IgG, suggesting that humoral immunity alone might be insufficient to clear infection, as demonstrated previously (6). Recovery occurred only after improving adherence and optimizing antiretroviral therapy on the basis of antiretroviral-resistance testing. This finding suggests that cell-mediated immunity is required for complete VACV clearance and that reversing any underlying immunosuppressive condition should be pursued whenever possible for recovery from progressive vaccinia (7) (Appendix Figure).
Molecular tests performed on serum and scab samples were positive for OPXV and VACV in March 2015 and remained positive in July 2015 (Table). To better characterize the VACV strain, we used specific primers targeting the A56R hemagglutinin gene (1,134 bp) for amplification and sequencing (3). Phylogenetic analysis (Appendix) confirmed infection with a VACV strain whose A56R gene sequence was closely related to those recently reported in Colombia and grouped as a sister lineage of the VACV group 1 in Brazil (Figure 2).
A biopsy of the persistent leg lesion collected in April 2016 tested negative for OPXV DNA by real-time PCR (Table) and positive for Pseudomonas aeruginosa and Escherichia coli by classic microbiological assays. The lesion healed after focused antimicrobial treatment.
The clinical case we describe meets all criteria for progressive vaccinia (4): immunodeficiency from HIV infection was documented with a CD4 cell count of <50 cells/mL; multiple lesions developed and failed to heal despite antimicrobial therapy; and VACV infection was confirmed by several laboratory methods. Our results document progressive vaccinia acquired through zoonotic transmission.
Because smallpox eradication led to the discontinuation of routine smallpox vaccination before the global spread of HIV, little is known about VACV infections in persons with HIV (8,9). Progressive vaccinia is thought to occur only in patients with substantial cell-mediated immunodeficiency (4). This hypothesis is further supported by the observation that VACV infection (through smallpox vaccination) in 10 HIV-infected persons with CD4 cell counts >200 cells/mL did not lead to progressive vaccinia (10). In the case we describe, VACV lesions persisted despite the documentation of VACV neutralizing antibodies. The lesions resolved only after immune reconstitution, indicating that cell-mediated immunity is required for complete viral clearance.
The persistent leg lesion was unexpected given the resolution of the patient’s other lesions and because latent VACV infection has not been described previously. Although testing of this lesion in July 2015 detected VACV, previous studies have demonstrated that VACV can be isolated from smallpox vaccination site lesions even after the separation of scab when the viral infection is presumably recovered (11). The positive bacterial cultures and absence of evidence of VACV in the lesion biopsy in April 2016 suggest that this lesion was most likely attributable to secondary bacterial infection resulting from the compromised dermal barrier rather than persistence or reactivation of latent VACV infection.
Our findings suggest that, in VACV infection cases, reversing any underlying immunosuppressive condition should be pursued whenever possible because of the potential role of the cellular immune response in clearing the infection. Because of waning global immunity against OPXVs (12), increasing immunosuppressed populations (13), and the potential nosocomial (14) and demonstrated zoonotic transmission of VACV (3), additional infection prevention, treatment, and control strategies are needed.
Ms. Laiton-Donato is a researcher in the Sequencing and Genomic Unit, Virology Group, at the Instituto Nacional de Salud, Colombia. Her research is focused on molecular virology of emerging viruses. Dr. Ávila-Robayo is a medical doctor at Hospital Universitario Mayor Méderi, Colombia. Her work focuses on the care of patients with infectious diseases.
We thank the following persons who provided essential assistance during the case investigation and subsequent laboratory testing of samples: Luis Ernesto Ayala, Faiber Antonio Gutierrez Lozada, Alberto de la Ossa, Rodrigo Posada and Juan Manuel Peláez Serna.
This work was supported by the Public Health Network at the Instituto Nacional de Salud, Colombia, and the US Centers for Disease Control and Prevention.
This study was performed in accordance with the ethical standards noted in the 1964 Declaration of Helsinki and its later amendments, and followed the national regulation contained in the 1993 resolution no. 008430 related to the ethical aspects of scientific research involving human beings where it is categorized as a minimal risk research. Samples were remitted to the Colombian National Institute of Health as part of the active virologic surveillance of potentially emerging threats.
- Fenner F, Henderson DA, Arita I, Jezek Z, Ladnyi ID. Smallpox and its eradication. 1988 [cited 2019 Sep 19]. https://apps.who.int/iris/handle/10665/39485
- Trindade GS, Emerson GL, Carroll DS, Kroon EG, Damon IK. Brazilian vaccinia viruses and their origins. Emerg Infect Dis. 2007;13:965–72.
- Usme-Ciro JA, Paredes A, Walteros DM, Tolosa-Pérez EN, Laiton-Donato K, Pinzón MD, et al. Detection and molecular characterization of zoonotic poxviruses circulating in the Amazon region of Colombia, 2014. Emerg Infect Dis. 2017;23:649–53.
- Bray M, Wright ME. Progressive vaccinia. Clin Infect Dis. 2003;36:766–74.
- Redfield RR, Wright DC, James WD, Jones TS, Brown C, Burke DS. Disseminated vaccinia in a military recruit with human immunodeficiency virus (HIV) disease. N Engl J Med. 1987;316:673–6.
- Bray M. Henry Kempe and the birth of vaccinia immune globulin. Clin Infect Dis. 2004;39:767–9.
- Letz AG, McFarland RW, Dice JP. Delay of chemotherapy to prevent progressive vaccinia. Mil Med. 2006;171:788–9.
- Amorosa VK, Isaacs SN. Separate worlds set to collide: smallpox, vaccinia virus vaccination, and human immunodeficiency virus and acquired immunodeficiency syndrome. Clin Infect Dis. 2003;37:426–32.
- Bartlett JG. Smallpox vaccination and patients with human immunodeficiency virus infection or acquired immunodeficiency syndrome. Clin Infect Dis. 2003;36:468–71.
- Tasker SA, Schnepf GA, Lim M, Caraviello HE, Armstrong A, Bavaro M, et al.; US Department of Defense Tri-Service AIDS Clinical Consortium. Unintended smallpox vaccination of HIV-1-infected individuals in the United States military. Clin Infect Dis. 2004;38:1320–2.
- Pittman PR, Garman PM, Kim SH, Schmader TJ, Nieding WJ, Pike JG, et al. Smallpox vaccine, ACAM2000: Sites and duration of viral shedding and effect of povidone iodine on scarification site shedding and immune response. Vaccine. 2015;33:2990–6.
- Reynolds MG, Carroll DS, Karem KL. Factors affecting the likelihood of monkeypox’s emergence and spread in the post-smallpox era. Curr Opin Virol. 2012;2:335–43.
- Parrino J, Graham BS. Smallpox vaccines: Past, present, and future. J Allergy Clin Immunol. 2006;118:1320–6.
- Zafar A, Swanepoel R, Hewson R, Nizam M, Ahmed A, Husain A, et al. Nosocomial buffalopoxvirus infection, Karachi, Pakistan. Emerg Infect Dis. 2007;13:902–4.
TableCite This Article
Original Publication Date: February 10, 2020
1These authors contributed equally to this article.