Article Text
Abstract
Objectives and design Using pol sequences obtained for routine resistance testing, we characterised the molecular patterns of HIV-1 transmission and factors associated with being part of a transmission cluster among individuals who in 2008–2014 presented with primary HIV-1 infection (PHI) at 11 urban centres across Italy.
Methods Pol sequences were obtained by Sanger sequencing. Transmission clusters were identified by phylogenetic analysis (maximum likelihood method, confirmed by Bayesian analysis). Multivariable logistic regression explored factors associated with a participant being part of a transmission cluster.
Results The PHI cohort comprised 186 participants (159/186, 85.5% males) with median age 44 years, median CD4 count 464 cells/mm3 and median plasma HIV-1 RNA 5.6 log10 copies/mL. Drug resistance associated mutations were found in 16/186 (8.6%). A diversity of non-B subtypes accounted for 60/186 (32.3%) of all infections. A total of 17 transmission clusters were identified, including 44/186 (23.7%) participants. Each cluster comprised 2–6 sequences. Non-B subtypes accounted for seven clusters and 22/44 (50%) of clustered sequences. In multivariable logistic regression analysis, factors associated with being part of a transmission cluster comprised harbouring a non-B subtype (adjusted OR (adjOR) 2.28; 95% CI 1.03 to 5.05; p=0.04) and showing a lower plasma HIV-1 RNA (adjOR 0.80, 95% CI 0.64 to 0.99; p=0.04).
Conclusions There was a large contribution of diverse non-B subtypes to transmission clusters among people presenting with acute or recent HIV-1 infection in this cohort, illustrating the evolving dynamics of the HIV-1 epidemic in Italy, where subtype B previously dominated.
- HIV
- MOLECULAR EPIDEMIOLOGY
- Disease Transmission, Infectious
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Footnotes
Handling editor Apostolos Beloukas
MRC and AB contributed equally.
GB and LF contributed equally.
Collaborators The INACTION study group participating physicians and centres are as follows: Andrea Gori, Antonio Muscatello, Alessandra Bandera (Ospedale Maggiore Policlinico Milano); Nicola Squillace (Monza); Giuseppe Tambussi, Silvia Nozza, Marco Ripa, Raffele Dell’Acqua, Elena Bruzzesi, Andrea Mastrangelo (H San Raffaele, Milano); Andrea Antinori, Carmela Pinnetti (INMI Spallanzani Roma); Andrea Calcagno, Gianfranco Orofino, Ilaria De Benedetto, Micol Ferrara (Torino); Cristina Mussini, Vanni Borghi, Federica Carli (Modena); Benedetto Maurizio Celesia (Catania); Lucio Cosco, Carlo Torti (Catanzaro); Gabriella D’Ettorre (Umberto I, Roma); Antonio Di Biagio, Lucia Taramasso (Genova); Emanuele Focà, Eugenia Quiros-Roland (Brescia); Antonina Franco (Siracusa); Diego Ripamonti, Franco Maggiolo (Bergamo); Roberto Gulminetti, Massimiliano Fabbiani (Pavia); Sandro Piga, Marzia Garau, Marco Campus (Cagliari); Stefano Rusconi, Tiziana Formenti, Arianna Gabrieli, Alessia Lai, Cecilia Bonazzetti, Andrea Giacomelli (H Sacco, Milano); Giulia Marchetti, Camilla Tincati (H San Paolo, Milano); Antonella Cingolani (H Gemelli, Roma); Giordano Madeddu (Sassari).
Contributors GB ad LF together with AG, MRC and AB conceived and drafted the present work, and they acted as liaisons for the study group. LF, IA and GB, under the supervision of AA and MRC, conducted the analyses. AM, LT, MF, SN, GT, SR, AG, EF, CP, GE, CM, VB, BMC, GM, ADB, DR, NS and AA were involved in clinical care, data collection and contributed to the writing of the manuscript. All authors revised the manuscript critically and approved the final version of the manuscript. All the authors listed have substantially contributed to the study's conception, design and/or performance.
Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.
Competing interests LT reports past (within 36 months) financial relationships (advisory board membership or consultancy fees, speakers’ honoraria or travel support) with Gilead Sciences, Janssen, Viiv Healthcare and no other conflict of interest. MF reports past (within 36 months) financial relationships (advisory board membership or consultancy fees, speakers’ honoraria or travel support) with Gilead Sciences, Janssen, Viiv Healthcare, BMS, MSD and no other conflict of interest. SR reports past (within 36 months) financial relationships (advisory board membership or consultancy fees, speakers’ honoraria or travel support) with Gilead Sciences, Janssen, Viiv Healthcare and no other conflict of interest. AG reports past (within 36 months) financial relationships (educational support) with Mylan and no other conflict of interest. EF reports past (within 36 months) financial relationships (advisory board membership or consultancy fees, speakers’ honoraria or travel support) with Gilead Sciences, Janssen, Viiv Healthcare, MSD and no other conflict of interest. CP reports past (within 36 months) financial relationships (advisory board membership or consultancy fees, speakers’ honoraria or travel support) with Janssen. GM reports past (within 36 months) financial relationships (advisory board membership or consultancy fees, speakers’ honoraria or travel support) with Gilead Sciences, Janssen, Viiv Healthcare, MSD and no other conflict of interest. AG reports past (within 36 months) grant/research supports, honoraria or consultation fees, speaker’s bureau compensation and/or travel support from Abbvie, Astellas, BMS, Boeringher, Gilead, Janssen, MSD, Novartis, Pfizer, Roche, ViiV and no other conflict of interest.
Provenance and peer review Not commissioned; externally peer reviewed.
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