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Antimicrobial Agents and Chemotherapy, June 1999, p. 1520-1522, Vol. 43, No. 6
0066-4804/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
In Vitro Antifungal Susceptibilities of
Scopulariopsis Isolates
C.
Aguilar,1
I.
Pujol,2 and
J.
Guarro1,*
Unitat de Microbiologia, Facultat de
Medicina, Universitat Rovira i Virgili,1 and
Laboratori de Microbiologia, Hospital Universitari de Sant
Joan de Reus,2 43201 Reus, Tarragona, Spain
Received 23 November 1998/Returned for modification 30 January
1999/Accepted 21 March 1999
 |
ABSTRACT |
MICs and minimum fungicidal concentrations of amphotericin B,
miconazole, itraconazole, ketoconazole, fluconazole, and flucytosine against 17 isolates of Scopulariopsis spp. were determined
by a broth microdilution method. All the isolates were resistant to
itraconazole, fluconazole, and flucytosine, and amphotericin B,
miconazole, and ketoconazole MICs were low for only a few.
 |
TEXT |
Scopulariopsis is a
large anamorphic genus comprising mainly soil species which are
frequently isolated from food, paper, and other materials and occur
also as laboratory contaminants. Scopulariopsis species are
among the most common nondermatophytic fungi that cause onychomycosis,
and they are also responsible, although less frequently, for
deep-tissue infections (4, 13, 17). In approximately 90% of
reported invasive infections caused by Scopulariopsis there
were some well-defined predisposing factors, the most frequent being
AIDS, organ transplantation, corticosteroid therapy, peritoneal
dialysis, surgery, cardiac diseases, and trauma, etc. Eight
species of Scopulariopsis have been reported as producing infections in humans, five of them causing only onychomycosis. They are
Scopulariopsis acremonium, S. asperula, S. flava, S. fusca, S. koningii, S. brevicaulis, S. brumptii, and S. candida. S. brevicaulis is the species most frequently associated with invasive infections (7). Some species of the ascomycete
genus Microascus, which comprises teleomorphs (sexual
states) of Scopulariopsis, have also been cited as
pathogenic to humans. They are Microascus cinereus, M. cirrosus, and M. manginii (7).
The majority of clinical cases have been treated with amphotericin B,
although many other antifungals have also been used. Very little
information exists about the in vitro activity of antifungals against
Scopulariopsis. In the majority of reports, only one strain
was tested and details about the technique used are generally scarce
(1, 2, 4, 5, 8, 9, 11, 13, 14, 20, 21). In this study, in
vitro antifungal susceptibilities of clinical and environmental
isolates of Scopulariopsis spp. were evaluated by the broth
microdilution method, broadly following the National Committee for
Clinical Laboratory Standards' guidelines (standard M38-P).
Broth microdilution method.
The method used was detailed
previously (18). A total of 17 isolates of
Scopulariopsis spp. were tested (Table
1). Antifungal agents included
amphotericin B (E.R. Squibb & Sons, Barcelona, Spain), flucytosine
(Hoffmann-La Roche, Basel, Switzerland), fluconazole (Pfizer,
Madrid, Spain), ketoconazole (Roig-Farma, Barcelona, Spain),
miconazole (Roig-Farma), and itraconazole (Janssen Pharmaceutica, Beerse, Belgium). Fungizone and Diflucan, the commercial
intravenous preparations of amphotericin B and fluconazole,
respectively, were used as stock solutions. The inoculum was 1 × 104 to 5 × 104 conidia per ml. The
concentrations of the test drug were 0.03 to 16 µg/ml for
amphotericin B, miconazole, itraconazole, and ketoconazole; 0.125 to 64 µg/ml for fluconazole; and 0.25 to 128 µg/ml for flucytosine. The
temperature of incubation was of 30°C, and MIC readings were made
after 48 and 72 h. The amphotericin B MIC was defined as the
lowest drug concentration with which there was a complete absence of
growth. MICs of the azoles and flucytosine were defined as the lowest
drug concentration that gave only slight growth, corresponding to
approximately 25% of the growth of the control. The minimum fungicidal
concentrations (MFC) were obtained by placing 10 µl from each well
which showed inhibition onto oatmeal plates. Fungal colonies were
counted after incubation for 48 h at 30°C. The MFC was defined
as the lowest drug concentration at which one colony or less was
visible on the agar plate. To compare the MIC readings at 48 and
72 h, differences of no more than 1 dilution (one well) were used
to calculate the percentage of agreement. The kappa test was used to
calculate the degree of agreement. A kappa value (
) greater than
0.75 was taken to represent excellent agreement, values below 0.40 were taken to represent poor agreement, and values between 0.40 and 0.75 were taken to represent fair to good agreement.
Table 1 shows that only some of the strains, belonging to different
species, displayed moderate susceptibility to amphotericin B,
miconazole, and ketoconazole. All of them were clearly resistant to
itraconazole, fluconazole, and flucytosine. S. carbonaria was the species for which MICs and MFCs were generally
the lowest. S. brevicaulis showed very variable results.
Amphotericin B MICs were relatively low for two of the five isolates,
miconazole MICs were low for three, and ketoconazole MICs were low for
four, although MICs were not lower than 1 µg/ml in any case. The MIC
ranges were generally wider and lower than the ranges of the MFCs.
Excellent agreement between the MICs at 48 and 72 h was shown for
itraconazole (
= 1), fluconazole (
= 1), flucytosine (
= 1),
and miconazole (
= 0.76). Good agreement was shown for ketoconazole
(
= 0.64), and poor agreement was shown for amphotericin B (
= 0.28).
Although amphotericin B is the drug most frequently used, the correct
treatment for invasive
Scopulariopsis infections is
still
unclear. The success rate of this drug is only about 40%.
On six
occasions amphotericin B was used alone (
11,
12,
15,
17,
22,
23), but on only three of them did the patients
make good
progress. One patient was first treated with different
doses of
amphotericin B without success, but the change to a liposomal
preparation of the same polyene compound resolved the infection
(
10). In another five patients, amphotericin B was used in
combination
with other antifungal drugs (ketoconazole for one patient,
miconazole
for another, and itraconazole for another three) (
4,
9,
15,
16,
19). Combined with itraconazole, amphotericin B
showed
good results on three occasions. Itraconazole was also
used alone for
one patient with ulcerous cheilitis (
1) and
one with plantar
infection (
5). The first patient relapsed
after a certain
degree of improvement, but the second was cured
completely after the
failure of ketoconazole and fluconazole.
Ketoconazole was effective for
the treatment of psoriasiform plaques
in a patient with human
immunodeficiency virus (
6), and miconazole
cured a mycotic
corneal ulcer which had developed after herpetic
keratitis
(
2). Flucytosine was used for only one patient with
mycetoma, in whom it was not effective (
3).
Results obtained by authors who have tested the in vitro antifungal
susceptibilities of
Scopulariopsis spp. are generally
contradictory, probably due to the variety of methods used. However,
in
only six articles were there details of the method employed
(
5,
9,
11,
14,
20,
21). In four of the studies the
agar dilution method
was used, a disc diffusion method was used
in another, and a broth
dilution method was used in the sixth.
Regli et al. (
20)
carried out the widest study, testing 38 strains
of
S. brevicaulis against 10 antifungal drugs. They compared three
solid
media (Sabouraud dextrose agar, yeast malt agar, and Casitone
agar) and
concluded that
S. brevicaulis was highly resistant to
griseofulvine, tolnaftate, amphotericin B, and flucytosine and
moderately sensitive to miconazole and ketoconazole. More data
about
the in vitro antifungal susceptibilities of clinical isolates
of
Scopulariopsis have appeared in some reports of human
infections
caused by these fungi (
1,
2,
4,
5,
9,
11,
13,
14,
21). Amphotericin B was defined as ineffective every time
it was
tested (seven times). MICs of fluconazole and flucytosine
were low for
only one of four and one of six isolates, respectively.
Miconazole and
ketoconazole showed high MICs for half of the assayed
isolates (2 of 4 in each case). Itraconazole, being active in
three of the five tests,
was the antifungal drug that showed the
lowest MIC in these clinical
reports, and another isolate was
defined as relatively sensitive. This
contrasts with our results,
where itraconazole MICs for none of the 17 strains could be considered
as indicating
activity.
In general, our data confirm the high in vitro resistance of
Scopulariopsis spp. reported by other authors. More data are
needed to draw more valid conclusions about the susceptibility
of
Scopulariopsis both in vitro and in vivo and to determine
whether
in vitro testing is more reliable with conidia than with hyphae
(
8). Every clinical case report would therefore need to
include
data on in vitro antifungal susceptibility testing, in which
the
method used, the MICs, the treatment, and the clinical outcome
would be described in detail. However, the data available make
us
pessimistic about an effective treatment for these infections,
although
the relative success shown by itraconazole in some clinical
cases
merits special attention. Experimental studies to test the
effectiveness of this drug alone and/or in combination with others
are
required to confirm the sparse clinical data that exist. The
finding of
new compounds active against this refractory fungus
constitutes a
priority challenge to modern
medicine.
 |
ACKNOWLEDGMENTS |
This work was supported by a grant from the Fundació
Ciència i Salut of Spain.
We thank M. G. Rinaldi for supplying some of the strains used in
this study.
 |
FOOTNOTES |
*
Corresponding author. Mailing address: Unitat de
Microbiologia, Facultat de Medicina, Universitat Rovira i
Virgili, Carrer Sant Llorenç, 21, 43201 Reus, Tarragona, Spain.
Phone: 977-759359. Fax: 977-759322. E-mail:
umb{at}astor.urv.es.
 |
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Antimicrobial Agents and Chemotherapy, June 1999, p. 1520-1522, Vol. 43, No. 6
0066-4804/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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