Surveillance of HIV-1 primary infections in France from 2014 to 2016: toward stable resistance, but higher diversity, clustering and virulence?
Adult
Anti-HIV Agents
/ pharmacology
Drug Resistance, Viral
/ genetics
Epidemiological Monitoring
Evolution, Molecular
Female
France
/ epidemiology
Genetic Variation
Genotype
HIV Infections
/ drug therapy
HIV-1
/ drug effects
Humans
Male
Middle Aged
Mutation
Phylogeny
Sequence Analysis, DNA
Sexual and Gender Minorities
Viral Load
Virulence
Journal
The Journal of antimicrobial chemotherapy
ISSN: 1460-2091
Titre abrégé: J Antimicrob Chemother
Pays: England
ID NLM: 7513617
Informations de publication
Date de publication:
01 01 2020
01 01 2020
Historique:
received:
27
05
2019
revised:
19
08
2019
accepted:
23
08
2019
pubmed:
24
10
2019
medline:
17
4
2021
entrez:
24
10
2019
Statut:
ppublish
Résumé
Patients with primary HIV-1 infection (PHI) are a particular population, giving important insight about ongoing evolution of transmitted drug resistance-associated mutation (TDRAM) prevalence, HIV diversity and clustering patterns. We describe these evolutions of PHI patients diagnosed in France from 2014 to 2016. A total of 1121 PHI patients were included. TDRAMs were characterized using the 2009 Stanford list and the French ANRS algorithm. Viral subtypes and recent transmission clusters (RTCs) were also determined. Patients were mainly MSM (70%) living in the Paris area (42%). TDRAMs were identified among 10.8% of patients and rose to 18.6% when including etravirine and rilpivirine TDRAMs. Prevalences of PI-, NRTI-, first-generation NNRTI-, second-generation NNRTI- and integrase inhibitor-associated TDRAMs were 2.9%, 5.0%, 4.0%, 9.4% and 5.4%, respectively. In a multivariable analysis, age >40 years and non-R5 tropic viruses were associated with a >2-fold increased risk of TDRAMs. Regarding HIV diversity, subtype B and CRF02_AG (where CRF stands for circulating recombinant form) were the two main lineages (56% and 20%, respectively). CRF02_AG was associated with higher viral load than subtype B (5.83 versus 5.40 log10 copies/mL, P=0.004). We identified 138 RTCs ranging from 2 to 14 patients and including overall 41% from the global population. Patients in RTCs were younger, more frequently born in France and more frequently MSM. Since 2007, the proportion of TDRAMs has been stable among French PHI patients. Non-B lineages are increasing and may be associated with more virulent CRF02_AG strains. The presence of large RTCs highlights the need for real-time cluster identification to trigger specific prevention action to achieve better control of the epidemic.
Identifiants
pubmed: 31641777
pii: 5602627
doi: 10.1093/jac/dkz404
doi:
Substances chimiques
Anti-HIV Agents
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
183-193Investigateurs
C Roussel
(C)
H Le Guillou-Guillemette
(H)
A Ducancelle
(A)
L Courdavault
(L)
C Alloui
(C)
P Honore
(P)
Q Lepiller
(Q)
D Bettinger
(D)
P Bellecave
(P)
P Pinson-Recordon
(P)
C Tumiotto
(C)
S Vallet
(S)
C Payan
(C)
J C Duthe
(JC)
M Leroux
(M)
J Dina
(J)
A Vabret
(A)
A Mirand
(A)
C Henquell
(C)
M Bouvier-Alias
(M)
A Simohamed
(A)
G Dos Santos
(G)
S Yerly
(S)
C Gaille
(C)
W Caveng
(W)
S Chapalay
(S)
A Calmy
(A)
A Signori-Schmuck
(A)
P Morand
(P)
C Pallier
(C)
M Raho-Moussa
(M)
M Mole
(M)
M-J Dulucq
(MJ)
L Bocket
(L)
K Alidjinou
(K)
S Ranger-Rogez
(S)
M A Trabaud
(MA)
V Icard
(V)
J C Tardy
(JC)
C Tamalet
(C)
C Delamare
(C)
B Montes
(B)
E Schvoerer
(E)
H Fenaux
(H)
A Rodallec
(A)
E André-Garnier
(E)
V Ferré
(V)
A De Monte
(A)
A Guigon
(A)
J Guinard
(J)
D Descamps
(D)
C Charpentier
(C)
B Visseaux
(B)
G Peytavin
(G)
P Tremaux
(P)
V Avettand-Fenoel
(V)
C Soulié
(C)
I Malet
(I)
M Wirden
(M)
A G Marcelin
(AG)
V Calvez
(V)
P Flandre
(P)
L Assoumou
(L)
D Costagliola
(D)
L Morand-Joubert
(L)
S Lambert-Niclot
(S)
D Fofana
(D)
N Boukli
(N)
C Delaugerre
(C)
M L Chaix
(ML)
N Mahjoub
(N)
C Amiel
(C)
G Giraudeau
(G)
A Beby-Defaux
(A)
D Plainchamp
(D)
A Maillard
(A)
E Alessandri-Gradt
(E)
M Leoz
(M)
J C Plantier
(JC)
P Gantner
(P)
H Delagreverie
(H)
S Fafi-Kremer
(S)
P Fischer
(P)
S Raymond
(S)
J Izopet
(J)
J Chiabrando
(J)
K Stefic
(K)
F Barin
(F)
G Fajole
(G)
O Burgault
(O)
S Marque-Juillet
(S)
Informations de copyright
© The Author(s) 2019. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For permissions, please email: journals.permissions@oup.com.