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Journal of Clinical Microbiology, January 1999, p. 258-260, Vol. 37, No. 1
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Case of Onychomycosis Caused by
Microsporum racemosum
Pedro
García-Martos,1
Josepa
Gené,2,*
María
Solé,2
José
Mira,1
Ricardo
Ruíz-Henestrosa,3 and
Josep
Guarro2
Servicio de
Microbiología1 and
Servicio de
Dermatología,3 Hospital
Universitario "Puerta del Mar," 11009 Cádiz, and
Unitat de Microbiologia, Facultat de Medicina i
Ciències de la Salut, 43201 Reus,2 Spain
Received 26 August 1998/Returned for modification 17 September
1998/Accepted 5 October 1998
 |
ABSTRACT |
We report the case of a Spanish 60-year-old female who presented in
1997 with onychomycosis of the left thumbnail following an injury
caused by a fresh fish bone. Microsporum racemosum was repeatedly cultured from nail scrapings, and its identity was confirmed
by sequencing the isolate's ITS1/ITS2 and 5.8S rRNA regions. The
patient was successfully treated with itraconazole, which was
administered for 12 weeks. This represents the first case of
onychomycosis due to M. racemosum and the first time that this species has been isolated from a human in Europe.
 |
TEXT |
Mycotic nail infections are caused
by dermatophytes, yeasts, and opportunistic filamentous fungi, such as
Scopulariopsis brevicaulis or Nattrassia
mangifera, among others (5, 6). These infections are
not readily treated, and the exact number of people affected is unknown
because adequate mycological studies are not always performed
(12) and cases are underreported. In our country, species of
Trichophyton are the most frequent causes of nail infections in humans, with T. rubrum and T. mentagrophytes
being the predominant species (7, 8, 13). The present report
records, for the first time, the isolation of Microsporum
racemosum from a human being in Europe. It was isolated from a
fingernail of an otherwise healthy woman.
Case report.
A 60-year-old female, a housewife, presented
herself to the Servicio de Dermatología del Hospital
Universitario "Puerta del Mar" with onychomycosis of the left
thumbnail. The disease appeared following an injury caused by a fresh
fish bone. The symptoms appeared 1 week later as a yellow, purulent
exudate and a slight perilesional erythema when the thumb became
painful. The patient was treated topically with an antiseptic and
antibiotics. Clinically, the infection was of the subungual type, with
the nail being soft, friable, and opaque and exhibiting various degrees
of onycholysis without hyperkeratosis. Since discomfort persisted, the
nail was surgically removed. Eight weeks later, the nail bed was
dystrophic, with hyperkeratosis and yellow nail tissue (Fig.
1). Direct microscopic examination of the
affected nail revealed the presence of scarce, hyaline, septate hyphal
elements. Treatment was initiated with itraconazole (100 g/day), which
was administered orally for 12 weeks and to which the patient responded
favorably; the patient was then discharged.
Scrapings of the lesion were cultured on Sabouraud dextrose agar with
chloramphenicol (0.05 mg/ml) and cycloheximide (0.5 mg/ml) and on
potato dextrose agar, incubated at 25°C. Both media gave rise to
cream-colored velvety colonies, which spread very rapidly and became
powdery, with a wine-red reverse. Abundant verrucose and moderately
thick-walled macroconidia, measuring 50 to 70 µm by 10 to 15 µm,
with 4 to 9 (to 11) septa, and numerous microconidia arranged in
grapelike clusters and measuring 4 to 7 µm by 2.5 to 3 µm had
developed (Fig. 2). The isolate was
morphologically identified as M. racemosum (4,
9). Additionally, the ITS1/ITS2 and 5.8 rRNA regions of the
isolate were sequenced according to the procedure described by Stchigel
et al. (15). Further comparison of the sequence obtained
with that of the ex-type strain of M. racemosum (CBS
450.65), verified by Y. Graeser (Humbolt University, Berlin, Germany),
confirmed the identity of the isolate. The isolate was subcultured
under various conditions and is maintained in the culture collection of
the Medical School, University Rovira i Virgili, as isolate FMR 6313. Living cultures of this isolate have been deposited in the
International Mycological Institute of England and in the
Centraalbureau voor Schimmelcultures of The Netherlands.

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FIG. 2.
Macro- and microconidia of M. racemosum. (A)
Phase-contrast optics (magnification, ×389); (B) Nomarski optics
(magnification, ×1,200).
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|
The geophilic dermatophyte
M. racemosum is the anamorph of
Arthroderma racemosum (
17), which belongs to the
order Onygenales.
It was isolated for the first time in 1965 by
Borelli from the
hair of a wild rat in South America (
2) and
in 1969 from Romanian
soil (
1). It is a rare fungus that
grows readily on common
culture media, with optimum growth at 23 to
28°C and poor growth
at 37°C.
M. racemosum shows certain
similarities with other
Microsporum species:
M. boullardi,
M. gypseum,
M. praecox, and
M. vanbreuseghemi.
However, macroscopically it is
distinguished by its cream-colored
colonies with a deep wine-red
reverse, and microscopically it
is distinguished by its moderately
thick-walled macroconidia,
which frequently have terminal filaments,
and its stalked microconidia
arranged in typical racemose clusters.
Although it has been considered
to be potentially pathogenic (
9,
14), human infections are
extremely rare (
11). In 1976 in the United States, the first
case was reported in a 79-year-old
white man with numerous lesions
on the forehead, scalp, and nape of the
neck (
3). The second
case, also from the United States, was
characterized by a macropapular
lesion on the hand of the patient
(
10). Apart from these cases,
only a few other reports of
its occurrence exist. This species
was isolated in Poland in a survey
of keratinophilic fungi in
a polluted area of Katowice (
16).
The present work represents
the first case of onychomycosis due to
M. racemosum and the first
time that this species has been
isolated from a human in
Europe.
 |
ACKNOWLEDGMENTS |
We thank L. Ajello (Emory University School of Medicine, Atlanta,
Ga.) for his critical comments and M. Pereiro-Miguens (Santiago de
Compostela, Spain) and Y. Graeser (Humbolt University, Berlin, Germany)
for their kind cooperation.
This work was supported by the "Fundació Ciència i
Salut" (Reus, Spain).
 |
FOOTNOTES |
*
Corresponding author. Mailing address: Unitat de
Microbiologia, Departament de Ciències Mèdiques
Bàsiques, Facultat de Medicina i Ciències de la Salut,
Universitat Rovira i Virgili, Carrer Sant Llorenç 21, 43201-Reus,
Tarragona, Spain. Phone: 34 977 75 93 59. Fax: 34 977 75 93 22. E-mail:
umb{at}fmcs.urv.es.
 |
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Journal of Clinical Microbiology, January 1999, p. 258-260, Vol. 37, No. 1
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.