Antifungal activity evaluation of the constituents of Haliclona baeri and Haliclona cymaeformis, collected from the Gulf of Thailand.

A new compound maleimide-5-oxime was isolated, together with 3,4-dihydroxybenzoic acid, tetillapyrone, from the ethyl acetate extract of the marine sponge Haliclona baeri while tetillapyrone, nortetillapyrone, p-hydroxybenzaldehyde and phenylacetic acid were isolated from the ethyl acetate extract of Haliclona cymaeformis, collected from the Gulf of Thailand. The structures of tetillapyrone and nortetillapyrone were re-examined using HMBC correlations. Maleimide-5-oxime, tetillapyrone and nortetillapyrone were found to be inactive against three human tumor cell lines (the estrogen-dependent ER(+) MCF-7, the estrogen-independent ER(-) MDA-MB-231 and NCI-H460. Maleimide-5-oxime, p-hydroxybenzaldehyde, phenylacetic acid, tetillapyrone and nortetillapyrone were evaluated for their growth inhibitory effect against seven yeasts and eight filamentous fungi. Only nortetillapyrone showed antifungal activity, with a preponderance on the dermatophytic filamentous fungi.


Introduction
The frequency of invasive fungal infection has risen substantially with the increasing numbers of immunocompromised patients, such as those infected with HIV, receiving cancer chemotherapy, immunosuppressive therapy, or treatment with broad-spectrum antibiotics [1]. The most frequently encountered infections are caused by the yeast Candida albicans and by species of filamentous fungus Aspergillus. Other fungal pathogens that have emerged in recent years include yeast species such as Candida glabata, C. krusei, C. tropicalis, Cryptococcus and Trichosporon and filamentous fungi such as Fusarium, Rhizopus and Rhizomucor [2]. On the other hand, dermatophytes, which invade and multiply in keratinized tissues [3] and cause infection, have a worldwide distribution with geographical differences in the incidence and prevalence of different dermatophyte species [4] and the most common agents belong to three genera: Epidermophyton, Trichophyton and Microsporum. Majority of clinically used antifungals suffer from various drawbacks in terms of toxicity, efficacy and cost, and their frequent use has led to the emergence of resistant strains. Hence, there is a great demand for novel antifungal agents belonging to the wide range of structural classes, selectively acting on novel targets with fewer side effects [5].
There is mounting evidence that fungi display highly specific adaptations in the marine environment that include the production of unique secondary metabolites antibiotics [1]. The fact that marine organisms contain secondary metabolites different from their terrestrial counterparts in structure and biological activity has led to the hypothesis that marine organisms may contain efficient antifungal compounds, with different modes of action and selective antifungal activity compared with human cells [6].
Sponges in the genus Haliclona are well-known for producing a variety of secondary metabolites, most commonly bioactive alkaloids [7] and many of which are cytotoxic [8]. Antifungal compounds isolated from Haliclona include haliclonadiamine, an alkaloid isolated from Haliclona sp. from Palau [9] and alkyl amino alcohols, halaminols A, B and C from the tropical marine sponge Haliclona sp., collected on the Great Barrier Reef [10].
In the course of our investigation on bioactive compounds from the marine sponges from the Gulf of Thailand, we have investigated the chemical constituents of the two marine sponges Haliclona baeri and Haliclona cymaeformis, collected from the coastal area of Chonburi Province and from Koh Chang, Trad Province, Eastern Thailand, respectively. Isolated from Haliclona baeri were a new maleimide-5-oxime (1), 3,4-dihydroxybenzoic acid (2), tetillapyrone (5 and 6) while Haliclona cymaeformis furnished, besides tetillapyrone (5 and 6), p-hydroxybenzaldehyde (3), phenylacetic acid (4) and nortetillapyrone (7 and 8) (Figure 1). We have also re-examined the structures of tetillapyrone and nortetillapyrone, previously reported by our group from Tetilla japonica [11], as well as investigated the antifungal activity of the isolated compounds.

Results and Discussion
We have previously reported isolation of tetillapyrone (5) and nortetillapyrone (8) from the marine sponge Tetilla japonica, collected from the Gulf of Thailand [11]. Though the structures of both compounds were established by 1 H, 13 CNMR, COSY, NOESY, HETCOR, HMBC and HRMS as well as by X-ray analysis in the case of tetillapyrone (5), there were still some uncertainties with respect to the pyrone moiety. The correlations observed in the HMBC spectrum for both compounds raised some doubts about the correct position of the hydroxyl and carbonyl groups of the pyrone ring. In addition, the data obtained from the X-ray analysis did not provide any evidence if a hydrogen atom was attached to the oxygen atom on C-2 or on C-6. Besides, the positions of the hydroxyl and carbonyl groups of the pyrone ring in the structure of nortetillapyrone (8) were opposite to those observed in the pryrone ring of tetillapyrone (5). All of these evidences, combined with the new isolation of more quantities of tetillapyrone and nortetillapyrone from the marine sponges H. cymaeformis and H. baeri, have led us to re-examine their structures by careful analysis of the HMBC spectra of both compounds.
The structure of tetillapyrone (5), previously proposed by us [11], was based on the fact that one carbon signal was missing in the 13 C NMR spectrum and thus the carbon signal at δ109.45 was attributed to C-3 and C-5 of the pyrone ring. As the protons of the methyl group (δ1.76s) on C-3 of the pyrone ring and the hydroxyl proton at δ11.28s, showed crosspeaks with the carbon at δ109.45, we have concluded that the hydroxyl group was on C-6. In fact, it is improbable that C-3 and C-5 could have the same chemical shift value as both carbons have completely different environment. Carefully examining the HMBC at 500 MHz spectrum of tetillapyrone (Table1), we have found that the methyl protons (δ1.78s) gave strong correlations to, besides C-4 (δ136.21), the carbons at δ109.43 (C-3), 150 54 (C-6) and 163.85 (C-2). This was very strange since the methyl protons were five bonds away from C-5. On the other hand, the hydroxyl proton at δ11.30 brs (OH-6) showed also correlation with the carbon at δ109.43 (C-3), which is also of five bonds distance. However, the only chance for this to happen is that tetillapyrone does not exist as only one compound (5) but instead as two compounds (5 and 6). Thus the correlations observed in the HMBC spectrum were due to the methyl protons (δ1.78s) with the carbons at δ150.54 (C-2 of compound 6) and δ163.85 (C-2 of compound 5), respectively. This also explains the correlation observed between the hydroxyl proton at δ11.30 brs (OH-2) and the carbon at δ109.43 (C-3) of compound 6.
It is interesting to note that in the structure previously proposed for nortetillapyrone (8), the positions of the hydroxyl and carbonyl groups of the pyrone moiety were opposite to those found in the structure 5 of tetillapyrone. Though, the HMBC spectrum showed strong correlation between H-3 (δ5.62) and the carbon at δ163.18, like that in structure 5 of tetillapyrone, the correlation between H-3 and the hydroxyl proton at δ 11.23 brs observed in the COSY spectrum, has led to the conclusion that nortetillapyrone should have the structure 8. In this structure, the chemical shift values of the carbonyl carbon (δ150.48) and the enolic carbon (δ163.18) were opposite to those found in tetillapyrone (5). However, there is no satisfactory explanation for this incongruence. The only possibility is, like in the case of tetillapyrone, nortetillapyrone also exists, in solution, as two compounds (7 and 8). In this circumstance, the correlation observed in HMBC spectrum ( Table 2) between H-4 (δ 5.52d) and the carbon at δ163.18 (C-2) was due to structure 7, while the correlation between H-4 (δ 5.52d) and the hydroxyl group at δ11.23 brs (OH-2), observed in the COSY spectrum, was due to structure 8.
Since structures 5 and 6 of tetillapyrone are tautomers, they can exist in equilibrium in the solution. In the same way, structures 7 and 8 are also tautomers of nortetllapyrone and thus can also exist in equilibrium in the solution (Figure 2).    Figure 2. Tautomerization of tetillapyrone (5, 6) and nortetillapyrone (6, 7).
The structure of compound 1 was identified as maleimide-5-oxime by spectroscopic and HRMS data. EIHRMS of compound 1 gave the molecular ion peak at 122.02723, indicating its molecular formula as C 4 H 4 N 2 O 2 (cald.122.02728). The 1 H and 13 C NMR spectra of compound 1 were very simple, showing the proton and chemical shift values very similar to those observed for 3methylmaleimide-5-oxime, previously isolated from the marine sponge Pseudoceratina purpurea by our group [12]. However, the 1 HNMR of compound 1 showed two doublets of two coupled protons at δ 7.40d (J=7.6 Hz) and 5.45d (J=7.6 Hz) instead of the signals of the vinylic methyl protons (δ 1.73d, J=0.9Hz) and a vinylic proton (δ 7.2.6d, J=0.9Hz).

Conclusion
As most antifungal compounds from marine origin are cytotoxic, consequently they have not generally been considered promising antifungal agents for clinical application [6]. Though many secondary metabolites from marine source were reported for their antifungal activity, their cytotoxic effect has not been measured. From this point of view, nortetillapyrone showed a very interesting biological activity profile. This compound not only selectively inhibits the growth of dermatophytes but also possesses no cytotoxicity against the tumor cell lines. Consequently, the structural feature of nortetillapyrone could serve as a model for development of a potential antifungal agent with therapeutic value.

General
1 H and 13 C NMR spectra were recorded at ambient temperature in CDCl 3 and DMSO on a Bruker AMC instrument operating at 300.12 and 75.47 MHz, respectively or a Bruker DRX instrument operating at 500, respectively 125 MHz. EI mass spectra were measured on a Hitachi Perkin-Elmer RMV-6M instrument. HRMS spectra were measured on a Kratos concept II 2 sector mass spectrometer. The accelerating voltage was 8 kV. Si gel for chromatography was silica gel 60 (0.2-0.5 mm Merck) for analytical work and for preparative work TLC silica gel 60 GF 254 Merck.

Animal material
Haliclona cymaeformis (Esper, 1794) order Haplosclerida, family Chalinidae, was collected by Scuba diving in the Gulf of Thailand near Koh Chang (2 meter depth), Trad Province in March 2004. Haliclona baeri (Wilson, 1952) was also collected by Scuba diving in the in the coastal area of Chonburi Province (3 meter depth). The sponge materials were identified by Dr. Sumaitt Putchakarn and the vouchers of the specimens, registered as BIMS-I 953 and BIMS-I 1766, respectively were deposited at Bangsaen Institute of Marine Science (BIMS), Burapha University, Bangsaen, Chonburi, Thailand. The materials were frozen immediately at -20ºC prior to extraction.

Extraction, isolation and characterization of the constituents of Haliclona baeri
The sample (1.3 kg net weight) was thawed, homogenized with EtOH (3 L), allowed to stand for 24 h in a dark chamber and filtered. The residue on the filter paper was again extracted with EtOH (2x3L), the aqueous alcoholic extracts were combined, evaporated at reduced pressure to ca. 500 ml and extracted with EtOAc (3x500mL). The EtOAc extracts were combined and concentrated at reduced pressure to give the crude EtOAc extract. This (10 g) was chromatographed over a Si gel column (120g) and eluted with petrol-CHCl 3

Extraction, isolation and characterization of the constituents of Haliclona cymaeformis
The sample of Haliclona cymaeformis (7.6 kg net weight) was thawed, homogenized with EtOH (10L), allowed to stand for 24 h in the dark chamber and filtered. The residue on the filter paper was again extracted with EtOH (2x10L), the aqueous alcoholic extracts were combined, evaporated at reduced pressure to give ca. 700 ml and extracted with EtOAc (3x1L). The EtOAc extracts were combined and concentrated at reduced pressure to give a crude EtOAc extract (21g). This extract was applied to flash chromatography column of Si Gel (150 g) and eluted with CHCl 3 (frs.

Cell Growth Assay
The effect of compounds on the growth of human tumor cell lines were evaluated according to the procedure adopted by National Cancer Institute (NCI, USA) for the in vitro anticancer drug discovery screen which uses the protein-binding dye sulforhodamine B (SRB) to assess cell growth inhibition [13,14] and according to the method described by Kijjoa et al. [15].