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Antimicrob Agents Chemother. Dec 2010; 54(12): 5391–5394.
Published online Oct 11, 2010. doi:  10.1128/AAC.00617-10
PMCID: PMC2981295

Caspofungin Affects Growth of Paracoccidioides brasiliensis in Both Morphological Phases [down-pointing small open triangle]

Abstract

Five Paracoccidioides brasiliensis isolates were grown in the presence of caspofungin (0 to 1 μg/ml). Inhibition of the yeast phase ranged from 20 to 65%, while in the mycelial form it ranged from 75% to 82%. Such variability was loosely related to the amount of cell wall β-1,3-glucan. No association with point mutations in the β-1,3-glucan synthase was detected. Caspofungin induced physical changes and cytoplasmic deterioration in both fungal phases.

The echinocandins, inhibitors of the β-1,3-d-glucan synthase, affect the assembly of the fungal cell wall, leading to cell deterioration (25). Candida and Aspergillus are caspofungin-sensitive genera (9, 15), while zygomycetes and other fungi are not (11). Dimorphic fungi, i.e., Blastomyces dermatitidis or Histoplasma capsulatum, are rather resistant (7). They and Paracoccidioides brasiliensis have β-1,3-glucan in their cell walls, mainly in their mycelial (M) phase. α-1,3-Glucan substitutes for β-1,3-glucan almost entirely when these species go into the pathogenic yeastlike (Y) phase (16-19). Herein, we report the effect of caspofungin in P. brasiliensis growth, cell wall composition, and morphology.

P. brasiliensis isolates IVIC Pb73 (ATCC 32071; patient), IVIC Pb300 (soil), IVIC Pb377 (armadillo), and IVIC Pb381 and IVIC Pb444 (recent isolates from patients) were grown for up to 4 days in RPMI 1640 (Gibco) medium buffered with 0.165 M morpholinepropanesulfonic acid (MOPS) to pH 7.0, according to CLSI M27-A2, in the presence of caspofungin (0 to 1.0 μg/ml). Y cells were incubated at 37°C; cell density was followed by turbidimetry in Klett units, every 24 h. Mycelia grew at 23°C; growth was measured daily by dry weight (20). Experiments were repeated three times.

The cell walls and fractions herein were prepared as before (20). Alkali-insoluble fraction 1 (β-1,3-glucan and chitin), alkali-soluble, acid-insoluble fraction 2 (α-1,3-glucan), and alkali- and acid-soluble fraction 3 (galactomannan, proteins, and lipids) were separated (20). Hexoses (for glucans) (21) and N-acetyl-hexosamine (for chitin) (1) were quantitatively traced in fractions 1 and 2. Fractionation was carried out twice, and chemical analyses were done in triplicate. Infrared (IR) spectroscopy with KBr pellets was performed with a Brucker FT_IR Tensor 27 infrared spectrometer (Elk Grove Village, IL). Transmission electron microscopy (TEM; Phillip CM10, Eindhoven, Netherlands) and scanning electron microscopy (SEM; Hitachi S-4500) were performed as before (2).

FKS1 gene fragments corresponding to Fks1 hot spot 1 and 2 regions were amplified. Fks protein sequences from Candida krusei (DQO17894), C. glabrata (AF229171), and C. albicans (D88815) were aligned with the protein sequence of P. brasiliensis FKS (AF148715) and the respective Fks sequences mined from the genomes of P. brasiliensis isolates Pb01, Pb18, and Pb03 (Broad Institute, MIT, Boston, MA; http://www.broadinstitute.org/annotation/genome/paracoccidioides_brasiliensis/MultiHome.html). Fks hot spots 1 and 2 were identified (5, 25); primers were designed on these regions, extending them about 100 bp upstream and downstream. The deduced amino acid sequences of Fks1 hot spot 1 and 2 regions in our P. brasiliensis isolates were compared by Clustal W (24).

Statistical analyses were done by covariance analysis (ANCOVA), with the SPSS 17.0 program, at a significance level representing P values of ≤0.05. They were run at different concentrations of caspofungin at each day, with every culture, and in both morphological phases.

The CLSI (formerly NCCLS) reference method (M38-A) (13, 14) is poorly suited to measure the in vitro activity of echinocandins against filamentous fungi (8). We adapted the method to macroculture conditions because P. brasiliensis requires continuous aeration and longer periods of time (3 to 4 days) to grow. The effects of caspofungin on P. brasiliensis growth are recorded in Tables S1 and S2 in the supplemental material. Caspofungin (1.0 μg/ml) inhibited mycelial growth in proportions that ranged between 75.4% ± 0.5% (Pb381) and 82.3% ± 1.8% (Pb73) (Table S1). Y cultures were less affected, from 20.7% ± 0.7% (Pb377) to 65.6% ± 1.1% (Pb73) (Table S2). Higher caspofungin concentrations (up to 16 μg/ml; not shown) did not improve these figures. Statistical analyses under each experimental condition indicated P values of ≤0.05 in all cases.

Hyphal morphology deteriorated in the presence of caspofungin (Fig. (Fig.1),1), not only through disappearance of the hyphal segments but with disorganization of organelles within the cytoplasmic structure and a coarser appearance of the outer cell wall. Y cells were similarly affected by caspofungin (Fig. (Fig.22).

FIG. 1.
Transmission (TEM) and scanning (SEM) electron micrographs of P. brasiliensis Pb73 in its mycelial phase. (A, B, and C) TEM of cultures grown for 4 days in the absence (A and B) and presence (C) of caspofungin (1 μg/ml). (D) Corresponding SEM ...
FIG. 2.
Transmission (TEM) and scanning (SEM) electron micrographs of P. brasiliensis Pb73 in its yeastlike phase. (A and B) TEM of cells grown for 4 days in the absence (A) and presence (B) of caspofungin (1 μg/ml). (C and D) Corresponding SEM for panels ...

Cell wall analyses (see Table S3 in the supplemental material) indicated the presence of β-1,3-glucan as the prevalent neutral polysaccharide in the M cell walls of all isolates, from 20.2% (Pb444) to 31.4% (Pb73) of the total wall. Instead, the Y cell wall reduced these amounts to between 3.9 and 10.6% (for Pb377 and Pb73, respectively), while replacing this polysaccharide with α-1,3-glucan (22.4 to 32.6% for Pb73 and Pb381, respectively). Chitin was three times more abundant in the Y cell walls than in the corresponding M cell walls.

IR spectra were characteristic of polysaccharides (Fig. (Fig.3),3), with a strong and wide band around 3,400 cm−1 (OH stretching) and additional bands at 2,921 cm−1 (C-H stretching), 1,641 cm−1 (OH twisting), 1,414 cm−1 (CH twisting), 1,211/1,242 cm−1 (C-O-C twisting), and 1,147 to 1,023 cm−1 (C-C stretching). Fraction 2 of all strains in their Y phase showed signals at 929, 851, and 823 cm−1, suggestive of α-1,3-linkages (3). The corresponding fraction 2 region in the M phases presented the band at 929 cm−1 as the only one in this region. Bands at 897 and 1,378 cm−1 were characteristic of β-glucan in fraction 1 of both phases (3). Since this fraction was composed of a mixture of chitin and β-1,3-glucan, spectra were the result of bands associated with both polysaccharides, with additional bands characteristic of chitin (1,557, 1,662, and 3,442 cm−1).

FIG. 3.
Infrared spectra of α-1,3-glucan (A), laminarin (β-1,3-glucan) (B), chitin (C), fraction 1 from P. brasiliensis Pb73 yeastlike phase (D), fraction 1 from P. brasiliensis Pb73 mycelial phase (E), fraction 2 from P. brasiliensis Pb73 yeastlike ...

Sequence analysis of the deduced PbFKS1p failed to show any point mutation in “hot spot” regions 1 and 2 (aa 641 to 649 and aa 1351 to 1358), respectively.

The inhibitory effect of echinocandins has been associated with a blockage in the synthesis of cell wall β-1,3-glucan through inhibition of the corresponding synthase (25). Resistance to echinocandin may be due to a lack of this polysaccharide (12), the presence of outer capsules (10), or melanin (4, 10, 23). Melanization reduced P. brasiliensis susceptibility to amphotericin B and also protected against azoles (4). In Candida isolates, resistance may be related, although not exclusively, to point mutations in the deduced amino acid sequence of the β-1,3-glucan synthase, specifically the so-called hot spot 1 and 2 regions (5, 25). This does not seem to apply to the β-1,3-glucan synthase in our P. brasiliensis isolates, inasmuch as their sequences on their hot spot 1 and 2 regions and those downloaded from the publicly released P. brasiliensis genomes (Pb01, Pb03, and Pb18; Broad Institute, MIT) are 100% identical. Whether some other point mutations are at work is an open question (25).

Recently (22), we confirmed the presence of α-1,3-glucan in the Y cell wall of P. brasiliensis, albeit with a different structural arrangement than that proposed before (18), a glucan that is also present in our 5 isolates (Fig. (Fig.3).3). Because of the small β-1,3-glucan amounts and high-level α-1,3-glucan contents in the Y cell wall, we hypothesized a minimal effect of caspofungin on this phase. Caspofungin (1 μg/ml) partially inhibited Y growth at different proportions: Pb73 (65%) > Pb381 (52%) > Pb300 (35%) ≈ Pb444 (34%) > Pb377 (20%) (see Table S2 in the supplemental material). This order kept no direct relationship with the amounts of α-1,3-glucan (Pb381 [32%] > Pb444 [24%] = Pb377 [24%] = Pb300 [24%] ≈ Pb73 [22%]), although a loose relationship to the amounts of β-1,3-glucan was noted (Pb73 [11%] ≈ Pb444 [8%] ≈ Pb300 [7%] ≈ Pb381 [6%] > Pb377 [4%]) (Table S3).

The M phases of all P. brasiliensis isolates were, as expected, highly susceptible to caspofungin, with inhibition varying from 74% (Pb444) to 81% (Pb73) in the following sequence: Pb73 > Pb300 > Pb377 ≈ Pb444 ≈ Pb381 (see Table S1 in the supplemental material). Results for the inhibitory capacity of micafungin in P. brasiliensis have been reported (12); although higher concentrations of the echinocandin were used, those results cannot be directly compared with ours, as different protocols were used (15). The sequence of inhibition was loosely related to the amount of β-1,3-glucan in the mycelial cell walls of the strains (Pb73 [31%] > Pb377 [27%] > Pb300 [25%] > Pb381 [22%] > Pb444 [20%]) (Table S3). In no case was a 100% inhibition achieved, even at concentrations as high as 16 μM caspofungin (not shown), for which 91% inhibition (the highest in our tests) was the observed value for isolate Pb73 in M phase. Similar observations were commented upon by Espinel-Ingroff et al. (8), who indicated that echinocandins do not generally yield 100% inhibition susceptibility endpoints, because of trailing growth; similar outcomes have been reported for Candida kefyr (6) and Aspergillus species (25), an effect explained as the result of a fungistatic, rather than fungicidal, activity (6) or lysis of hyphal tips but not subapical hyphal compartments (25).

The possibility of using combinations of antifungals to improve the inhibitory capacity of caspofungin against P. brasiliensis remains to be studied.

Supplementary Material

[Supplemental material]

Acknowledgments

Acknowledgements are due to Merck, Sharp & Dohme (Caracas, Venezuela) for partial financial support, to Mirtha Romano (IVIC, Caracas, Venezuela) and Antonio Bretaña (Universidad Nacional Experimental Simón Rodríguez, Caracas, Venezuela) for transmission and scanning electron micrographs, respectively, to Pedro Moncada (Universidad Simón Bolívar, Caracas, Venezuela) for infrared spectra and Maria de Lourdes Corradi da Silva (Universidade Estadual Paulista, São Paulo, Brazil) for help in their interpretation, and to María de Lourdes González for statistical analyses.

Footnotes

[down-pointing small open triangle]Published ahead of print on 11 October 2010.

Supplemental material for this article may be found at http://aac.asm.org/.

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