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Volume 32, Number 9—September 2026

Research

Invasive Wickerhamomyces anomalus Infections among Injecting Drug Users, France, 2012–20241

Maxime Lefranc2, Adrien Pain2, Fréderic Dalle, Pierre Baudino, Claudio Plaisant, Taieb Chouaki, Josephine Dorin, Anne-Pauline Bellanger, Julie Bonhomme, Maxime Moniot, Celia Rouges, Françoise Botterel, Gregoire Pasquier, Lilia Hasseine, Estelle Perraud-Cateau, Jean-Pierre Gangneux, Laurence Delhaes, Damien Costa, Juliette Guitard, Alexandre Alanio, Valerie Letscher-Bru, Emilie Guemas, Guillaume Desoubeaux, Karine Boukris-Sitbon, Olivier Lortholary, Fanny Lanternier, Marie Desnos-Ollivier, Sebastien ImbertComments to Author , and WAIT-IV Study Group,3
Author affiliation: CHU Bordeaux, Bordeaux, France (M. Lefranc, P. Baudino, C. Plaisant, L. Delhaes, S. Imbert); Université de Bordeaux, Bordeaux, France (M. Lefranc, S. Imbert); Institut Pasteur, Paris, France (A. Pain, K. Boukris-Sitbon, O. Lortholary, M. Desnos-Ollivier, F. Lanternier); CHU Dijon, Dijon, France (F. Dalle); CHU Amiens-Picardie, Amiens, France (T. Chouaki); CHU d’Antibes Juan les Pins, Antibes, France (J. Dorin); CHU de Besançon, Besançon, France (A.-P. Bellanger); CHU Caen, Caen, France (J. Bonhomme); CHU Clermont-Ferrand, Clermont-Ferrand, France (M. Moniot); AP-HP Hôpital Cochin, Paris (C. Rouges); CHU Henri Mondor, Créteil, France (F. Botterel); CHU de Montpellier, Montpellier, France (G. Pasquier); CHU Nice, Nice, France (L. Hasseine); CHU Poitiers, Poitiers, France (E. Perraud-Cateau); CHU de Rennes, Rennes, France (J.-P. Gangneux); CHU de Rouen, Rouen, France (D. Costa); Sorbonne Universite, Paris (J. Guitard); Hôpital Saint-Antoine, Paris (J. Guitard); Hôpital Saint-Louis, Paris (A. Alanio); Hôpitaux Universitaires de Strasbourg, Strasbourg, France (V. Letscher-Bru); CHU Toulouse, Toulouse, France (E. Guemas); CHU de Tours, Tours, France (G. Desoubeaux)

Main Article

Table

Demographic and clinical characteristics of invasive Wickerhamomyces anomalus infection cases reported through multicentric prospective national surveillance programs, France, 2012–2024*

Characteristic All patients, N = 35 IDU, n = 26 Non-IDU, n = 9 p value†
Age median (IQR)
42 (36–50)
41 (36–45)
55 (36–68)
0.11
Sex
M 27/35 (77) 20/26 (77) 7/9 (78) >0.9
F




Invasive fungal disease 0.6
Fungemia 31/35 (89) 22/26 (85) 9/9 (100)
Osteoarticular infection
4/35 (11)
4/26 (15)
0/9 (0)

IFD risk factor other than IDU‡
HIV infection 2/31 (6.5) 2/26 (7.7) 0/5 (0) >0.9
Recent surgery 2/35 (5.7) 0/26 (0) 2/9 (22) 0.061
Central vascular catheter 9/35 (26) 2/26 (7.7) 7/9 (78) <0.001
Intensive care unit 7/35 (20) 3/26 (12) 4/9 (44) 0.055
Other underlying conditions‡ 4/35 (11) 1/26 (4) 4/9 (33) 0.010
>1 risk factor other than IDU 13/35 (37) 6/26 (23) 8/9 (89) <0.001
IFD history
8/33 (24)
7/25 (28)
1/8 (13)
0.6
Community onset
17/34 (50)
16/26 (62)
1/8 (13)
0.039
Associated deep-seated IFD 0.8
Spondylodiscitis 3/35 (8.6) 3/26 (12) 0/9 (0)
Septic arthritis 2/35 (5.7) 2/26 (7.7) 0/9 (0)
Endocarditis 1/35 (2.9) 1/26 (3.8) 0/9 (0)
Endophthalmia 1/35 (2.9) 1/26 (3.8) 0/9 (0)
None
28/35 (80)
19/26 (73)
9/9 (100)

Bacterial co-infection 8/35 (23) 5/26 (19) 3/9 (33) 0.4
Invasive fungal co-infection
7/35 (20)
4/26 (15)
3/9 (33)
0.3
First-line antifungal treatment 0.5
Echinocandin monotherapy 25/35 (71) 19/26 (73) 6/9 (67)
Fluconazole monotherapy 3/35 (8.6) 3/26 (12) 0/9 (0)
Voriconazole monotherapy 2/35 (5.7) 1/26 (3.8) 1/9 (11)
Combination therapy 2/35 (5.7) 1/26 (3.8) 1/9 (11)
No antifungals
3/35 (8.6)
2/26 (7.7)
1/9 (11)

Median length of hospital stay, d (IQR)
15 (7–31)
12 (6–23)
55 (22–64)
0.005
Recurrence
5/30 (17)
5/22 (23)
0/8 (0)
0.3
90-d all-cause mortality 1/30 (3.3) 0/22 (0) 1/8 (13) 0.3

*Values are no. (%) except as indicated. Data reported through Reseau de Surveillance des Infections Fongiques invasives (RESSIF) and Surveillance des Infections Fongiques Invasives (SINFONI). Denominators lower than the N/n value for each category indicate missing data. IDU, injecting drug user; IFD, invasive fungal disease; IQR, interquartile range. †Determined by Wilcoxon rank sum test or Fisher exact test. ‡Other underlying conditions were hematologic malignancy (n = 1), solid organ malignancy (n = 1), premature neonate (n = 1), and severe malnutrition (n = 1).

Main Article

1Preliminary results from this study were presented at ESCMID Global 2025; April 11–15, 2025; Vienna, Austria; and at the annual congress of the Société Française de Mycologie Médicale; June 18–20, 2025; Amiens, France.

2These authors contributed equally to this article.

3Additional members of the WAIT-IV Study Group are listed at the end of this article.

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Page updated: August 17, 2026
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