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Revista Peruana de Medicina Experimental y Salud Publica

Print version ISSN 1726-4634

Rev. perú. med. exp. salud publica vol.38 no.1 Lima Jan-Mar 2021  Epub Dec 20, 2020

http://dx.doi.org/10.17843/rpmesp.2021.381.5527 

Brief report

Transmitted resistance in HIV-1 of patients from nine departments of Peru

Carlos A. Yabar, Biologist, Doctor in Biological Sciences
http://orcid.org/0000-0002-9607-5693

Giovanny F. Vilcarino, Biologist
http://orcid.org/0000-0001-6031-5571

Susan Espetia, Biologist, Master in Microbiology
http://orcid.org/0000-0002-1160-9677

Mariela G. Yaya, Biologist
http://orcid.org/0000-0002-8009-1429

Gabriela Salinas, Biologist
http://orcid.org/0000-0001-7291-3528

Lisset García-Fernández, Physician, Master in Public Health
http://orcid.org/0000-0002-8821-6855

Rubén D. Vásquez Becerra, Physician, Master in Public Health
http://orcid.org/0000-0001-6384-5658

Carlos Benites, Physician
http://orcid.org/0000-0002-1795-7074

Daniel Santos-Anaya, Medical Technologist, 0000-0003-1010-0278

Edgardo Mamani, Biologist, Master in Biotechnology
http://orcid.org/0000-0001-5292-8327

Maribel Acuña, Biologist
http://orcid.org/0000-0001-9236-2014

Soledad Romero, Biologist
http://orcid.org/0000-0002-1360-9582

Fany Cárdenas, Biologist
http://orcid.org/0000-0002-4541-275X

1 Laboratorio de VTS/VIH-SIDA, Instituto Nacional de Salud, Lima, Perú

2 Universidad San Martín de Porres, Lima, Perú

3 Ministerio de Salud del Perú, Lima, Perú

4 Hospital Nacional María Auxiliadora, Lima, Perú

5 Dirección de Prevención y Control de VIH-SIDA, Enfermedades de Transmisión Sexual y Hepatitis, Ministerio de Salud, Lima, Perú

INTRODUCTION

HIV/AIDS affects more than 36 million people worldwide; although the pandemic is still on the rise, the AIDS mortality rate has declined by as much as 34%, mainly due to increased antiretroviral therapy (ART) coverage 1.

It should be noted that when a resistant HIV genotype is transmitted to a healthy or previously infected person, it will result into transmitted resistance (TR) 2, which is related to the risk of virologic failure in patients that initiate ART 3. In this regard, it is important to identify and perform surveillance of TR through HIV genotyping tests 2.

Regarding the prevalence of TR in Latin American and Caribbean (LAC) countries, a recent systematic review conducted on 81 studies between 2006 and 2015 revealed a frequency of 7.7% 4. Likewise, a review conducted on 358 studies in 64 countries revealed that the prevalence of TR in LAC was 12%, higher than Asia (2%) and Africa (9%) 5.

Among the socioepidemiological factors related to TR, associations have been found between the population of men who have sex with men (MSM) 6, virological failure 7 and with sexually transmitted infections (STIs) 8, suggesting that there is not necessarily a common factor associated with TR.

Most of the studies of TR in Peru were conducted in the city of Lima and showed that prevalence ranges from 1% to 14% 10 - 12. These differences in the prevalence of TR could be related to the study period, methodological design, type of genotypic test used, size, origin and characteristics of the participants in each study.

Likewise, it is not known whether the frequency of TR in Lima is similar to that of other Peruvian departments, since the transmission dynamics in the capital city are different from those in the rest of the country 13. In addition, socioepidemiological factors in Peruvian patients with TR have not been described. Therefore, the aim of this study was to estimate the frequency of TR in ART-naive HIV/AIDS patients in nine Peruvian departments. Additionally, the socioepidemiological factors found in the participants were described.

KEY MESSAGES

Motivation for the study: The study resulted from the lack of information at the national level on the situation of transmitted resistance (TR) to antiretrovirals in the Peruvian population.

Main findings: This study showed that TR is moderate according to World Health Organization (WHO) classification.

Implications: Improvement of public policies for treatment and sex education campaigns, in order to help decrease TR cases throughout Peru.

THE STUDY

A descriptive, cross-sectional study was carried out between July 2014 and December 2015 in 29 of the 79 public health facilities of the Peruvian Ministerio de Salud. These centers were selected because they cover 87.9% of patients that initiated ART nationwide 13 and correspond to nine Peruvian departments (Arequipa, Ica, Junín, Lambayeque, La Libertad, Lima, Loreto, Piura, and San Martín).

The sample size was calculated using the statistical program Epidat version 3.1, considering a prevalence of TR of 7.7% 4, assuming an absolute error of 5%, a 95% confidence level and a data loss rate of 20%, with which we established that at least 132 patients would be included. Table 1 shows the distribution of participants by department. The type of sampling applied was consecutive non-probabilistic, including patients of both sexes with at least 18 years of age, confirmed HIV diagnosis by ELISA, Western Blot, linear immunoblot assay (LIA) or indirect immunofluorescence (IFI), without previous ART. Patients with mental disorders and pregnant women were not considered.

Table 1 Socio-epidemiological and virological characteristics of the study sample. 

Characteristics n (%) / mean ± SD
Age 35.1 ± 10.77
Sex
Female 26 (19.3)
Male 109 (80.7)
Department of residence
Arequipa 6 (4.4)
Ica 3 (2.2)
Junín 10 (7.4)
La Libertad 7 (5.2)
Lambayeque 16 (11.9)
Lima/Callao 41 (30.4)
Loreto 17 (12.6)
Piura 3 (2.2)
San Martín 32 (23.7)
Years with HIV diagnosis †
Arequipa 2.00 ± 1.79
Ica 4.00 ± 5.66
Junín 1.40 ± 1.26
La Libertad 1.86 ± 1.86
Lambayeque 2.56 ± 1.41
Lima/Callao 1.90 ± 2.35
Loreto 1.25 ± 2.14
Piura 1.67 ± 1.15
San Martín 0.90 ± 0.49
Total 1.67 ± 1.89
Clinical status
AIDS 45 (33.3)
Not AIDS 78 (57.8)
Not established 12 (8.9)
Sexually Transmitted Infection
Yes 43 (33.1)
No 81 (62.3)
Not specified 6 (4.6)
Virological and immunological status
Viral load (copies/mL) 247,150.8 ± 39,194.7
CD4 cell count (cells/µL) 282.6 ± 222.7

† Time since HIV infection was first detected to enrollment in the study.

n: number of participants; SD: standard deviation.

The ethical principles established during the informed consent (IC) procedure followed during patient recruitment. In addition, participants completed a written survey to collect socio-epidemiological and clinical information about them. Peripheral blood samples were then collected and transferred to the National Referral Laboratory for STD/HIV-AIDS of the Instituto Nacional de Salud (INS) in Lima in sealed boxes labeled with the place of origin. Patient information was entered in an Excel database with restricted access and in charge of the principal investigator, while the ICs were archived under lock to ensure the confidentiality of the participants.

For HIV genotyping, a 1020 bp region was amplified by two rounds of PCR 14 and then, the sequence was determined by the Sanger method using the ABI 3500 XL genetic analyzer (Thermo Fisher Scientific®, United Kingdom). Samples that did not amplify by the In-House platform were handled using the commercial Trugene® method (Siemens Healthcare Diagnostics Inc. Deerfield, Illinois, USA). The consensus sequence was obtained using the RECall program (beta v3.05) 15.

To perform the analysis of resistance mutations, the sequences were entered into the HIVdb Program (https://hivdb.stanford.edu/hivdb/by-mutations/ ) of the Stanford University HIV Drug Resistance Database version 8.8, while the quality control of the sequences was performed with the World Health Organization (WHO) Quality Control Tool (https://pssm.cfenet.ubc.ca/who_qc).

Viral load was determined by an automated (Cobas) real-time PCR system using Taqman probes (Roche, Branchburg, USA), while CD4/CD8 count was performed by flow cytometry through the BD Multitest™ IMK kit and Facscanto II cytometer (BD).

The data collected were processed with the Stata v14.2 statistical package (Stata Corporation, College Station, Texas, USA). Descriptive results were obtained by using proportions for qualitative variables (department of residence, clinical status, sexually transmitted infection, type of STI and mutation identified) and mean with standard deviation for quantitative variables: age, time of diagnosis (years), number of sexual partners in the last year, number of sexual partners in the last six months, CD4, CD8 and CD3 cell counts, viral load (copies/mL), viral load (log10). Resistance, viral load and CD4/CD8 results were reported in the INS NetLab system (https://www.netlab.ins.gob.pe/FrmNewLogin.aspx) for the treatment of participants by their treating physicians.

The project was approved by the Institutional Research Ethics Committee of the INS with code OI-094-13.

FINDINGS

A total of 135 participants with HIV diagnosis were recruited from different regions of the country (Table 1). The population was characterized by being mostly male (80.7%) with a mean age of 35.1 ± 10.8. We also found that patients residing in Ica had HIV diagnosis for the longest time (4.00 ± 5.66 years) while those from San Martin had a more recent time of diagnosis (0.90 ± 0.5 years). The virological and immunological status of the participants revealed 247 150.8 ± 39 194.7 RNA copies/mL and CD4 lymphocyte count of 282.6 ± 222.7 cells/mL, with 33.3% of patients in the AIDS phase and 90.7% of STIs in the male population.

The genotype of 132 participants was analyzed. Three HIV samples were excluded because they were not reactive to RT-PCR and sequencing tests, both in-house and commercially available. The frequency of TR in the studied population was 9.8% (13/132), with five cases in Lima, four in San Martín, two in Lambayeque and one each in La Libertad and Piura.

Analyzing TR by department and according to the type of antiretroviral (ARV), a higher frequency was observed for the non-nucleoside reverse transcriptase inhibitor (NNRTI) group (6.1%, 8/132), with Lima and San Martín reporting the highest rates (Table 2). ARV resistance mutations were mainly associated with NNRTI (n = 10; 7.6%), predominantly the E138A mutation (2.3%), which confers a low level of resistance to rilpivirine (RPV) (Table 3). Likewise, we also observed the K103N mutation (1.5%), which is associated with a high level of resistance to efavirenz and nevirapine. The analysis of socio-epidemiological factors revealed that the mean number of sexual partners in the last year was higher in those patients who presented TR (10.8 ± 27.5) (Table 4).

Table 2 Frequency of antiretroviral-resistant HIV genotype according to department and according to the antiretroviral group used. 

Department n Resistance to any ARV n (%) Resistance to PI n (%) Resistance to NRTI n (%) Resistance to NN- RTI n (%)
Arequipa 6 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0)
Ica 3 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0)
Junín 10 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0)
La Libertad 7 1 (14.3) 0 (0.0) 0 (0.0) 1 (14.3)
Lambayeque 15 2 (13.3) 0 (0.0) 0 (0.0) 2 (13.3)
Lima/Callao 40 5 (12.5) 1 (2.5) 0 (0.0) 4 (10.0)
Loreto 17 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0)
Piura 3 1 (33.3) 1 (33.3) 0 (0.0) 0 (0.0)
San Martín 31 4 (12.9) 2 (6.5) 1 (3.2) 1 (3.2)
Total 132 13 (9.8) 4 (3.0) 1 (0.8) 8 (6.1)

n: number of participants; ARV: antiretroviral; PI: protease inhibitor; NRTI: nucleoside reverse transcriptase inhibitor; NNRTI: non-nucleoside reverse transcriptase inhibitor.

Table 3 Frequency of resistance mutations identified according to type of antiretroviral 

Associated mutation n (%) ARV RL
PI
Q58E 3 (2.3) FPV Low
L10F 1 (0.7) TPV Low
Total 4 (3.0)
NRTI
T215N 1 (0.7) AZT, D4T Low
Total 1 (0.7)
NNRTI
E138A 3 (2.3) RPV Low
K103N 2 (1.5) EFV, NVP High
V106I 2 (1.5) DOR Low
V108I 2 (1.5) NVP Low
A98G 1 (0.8) DOR, EFV, RPV Low
Total 10 (7.6)

PI: protease inhibitors; NRTI: nucleoside reverse transcriptase inhibitors; NNRTI: non-nucleoside reverse transcriptase inhibitors; n: total number of mutations; ARV: antiretroviral affected by mutation; RL: resistance level according to HIV db classification of the HIV Drug Resistance Data Base Program of Stanford University; FPV: fosamprenavir; TPV: tripnavir; AZT: zidovudine; D4T: stavudine; NVP: nevirapine; RPV: rilpivirine; EFV: efavirenz; DOR: doravirine.

Table 4 Transmitted resistance to antiretrovirals in HIV-1 according to socio-epidemiological, virological and immunological characteristics. 

Characteristics No resistance With resistance (n=13)
n Mean ± SD Mean ± SD
Age 116 35.4 ± 10.9 32.9 ± 9.5
Time to diagnosis (years) 114 1.7 ± 2.0 1.3 ± 0.9
Number of sexual partners in the last year 111 6.7 ± 29.9 10.8 ± 27.5
Number of sexual partners in the last 6 months 111 3.7 ± 17.6 0.8 ± 1.3
CD4 cell count (cells/µL) 117 274.0 ± 220.3 274.7 ± 170.4
CD8 cell count (cells/µL) 117 1,054.9 ± 561.9 804.9 ± 573.8
CD3 cell count (cells/µL) 117 1,380.4 ± 693.2 1,141.5 ± 718.2
Viral load (copies/mL) 118 259,740.2 ± 407,699.8 151,753.7 ± 199,932.0
Viral load (log10) 118 5.0 ± 0.7 4.8 ± 0.7

n: number of participants; SD: standard deviation.

DISCUSSION

According to our findings, the frequency of TR in Peru (9.8%), corresponds to a moderate level of resistance according to WHO 16, similar to what other LAC countries (from 8.2% to 12.8%) reported between 2014 and 2016 4.

In contrast to our study, Lama et al. 9 ) reported a TR frequency of 3.3%, despite the fact that the study population corresponded to MSM, which is characterized by high-risk sexual behavior for HIV/STI transmission 17. This value is probably related to the period in which the study was conducted, when ART in Peru was just beginning to be implemented, shortly after WHO began monitoring the drug resistance emergency 16.

On the other hand, the mutations identified in this study were mostly related to NNRTI resistance, in concordance with the resistance recently described in MSM and transgender population in Lima 12 and with different reports in LAC countries 5 , 6. Likewise, TR compared with NNRTIs could be related to acquired resistance in the Peruvian population, where we recently identified a high prevalence of NNRTI resistance 18.

On the other hand, the studies reported by Soria et al. 10 , 11 conducted in the city of Lima revealed considerable differences in TR in two time periods, from a low level (1% between 2007 and 2009) to a high level (14% between 2014 and 2015), which suggests that TR is experiencing an increase over time, as has been reported in other countries, where TR rose from low to moderate in only six years 16. These data suggest the need for longitudinal studies or periodic national surveillance to identify changes in TR over time, in order to take appropriate prevention measures and reduce HIV transmission in the population.

It should be noted that among the socio-epidemiological factors studied, we identified that the mean number of sexual partners in the last year was higher in the group that presented TR. Although these findings are descriptive, they suggest that sexual promiscuity could be playing an important role in the transmission of resistant strains of HIV, which could explain the high prevalence of TR found in MSM and transgender population in Lima 12 and in other related studies 4 , 5.

The main limitation of this study is the time elapsed since the samples were collected (>5 years). However, we consider that the findings described in this article will help to better understand the phenomenon of TR in Peru, which will allow us to propose new public health policies focused on generating changes in first-line ART strategies through early identification of the resistant genotype.

In conclusion, our study shows that TR in Peru is moderate, mainly to NNRTI, highly prevalent in coastal and jungle departments, and in people with multiple sexual partners. Consequently, further surveillance studies are required to determine the current situation of TR in Peru, as well as its associated factors.

Acknowledgments:

The authors thank Reyna Mayta, Lita Alarcón (Hospital Regional Las Mercedes, Lambayeque) Margarita Pinedo (Hospital de Ferreñafe, Lambayeque), Nidia Calderón (Hospital Regional de San Martín), Heriberto Arévalo and Yolanda Monteza (Laboratorio Regional de San Martín), Raul Montalvo and Omar Orellana (Hospital Regional de Junín) for their collaboration, Juan Díaz, Nancy Brizuela (Hospital Regional de Ica), Angélica García, Mariza Rojas, (Hospital Docente de Trujillo), María Gonzales, Lucía Gonzales and Gonzalo Castañeda (Hospital Regional de Arequipa), Cesar Ramal (Hospital Regional de Iquitos), Cesar Guerrero (Hospital Regional de Piura), María Dedios (Hospital Santa Rosa), Eduardo Sánchez (Hospital Hipólito Unanue), Jorge Arévalo (Hospital Dos de Mayo), Patricia Gonzales (Hospital María Auxiliadora), Augusto Escalante (Hospital San José), Miguel Estela (Hospital de Huacho) for their effort and support in the process of recruitment, survey and sampling of the study participants, without whom this research could not have been carried out. The authors would also like to thank Dr. Gilmer Solís Sánchez for his advice in the analysis and interpretation of the statistical data.

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Funding: The article was fully funded by the Instituto Nacional de Salud.

Cite as: Yabar CA, Vilcarino GF, Espetia S, Yaya MG, Salinas G, García-Fernández L, et al. Resistencia transmitida en VIH-1 de pacientes provenientes de nueve departamentos del Perú. Rev Peru Med Exp Salud Publica. 2021;38(1):77-82. doi: https://doi.org/10.17843/rpmesp.2021.381.5527.

Received: April 03, 2020; Accepted: October 07, 2020

Correspondence: Carlos Augusto Yabar; Av. Defensores del Morro 2268, Chorrillos, Lima, Perú; cyabar@ins.gob.pe

Authorship contributions:

CAY participated in the conception of the article, analysis and interpretation of data, writing and approval of the final version of the article. GFV, SE, MGY, GS, LGF, RDVB, CB, DSA, EM, MA, SR and FC participated in the analysis and interpretation of data, critical revision and approval of the final version of the article. SE, MGY, DSA, EM, MA, SR and FC participated in data collection. All authors assume responsibility for the contents of the manuscript.

Conflicts of interest:

The authors declare that they have no conflicts of interest.

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