INTRODUCTION

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Penicilliosis, caused by the dimorphic fungus Penicillium marneffeia facultative intracellular pathogen for humansis a disseminated and progressive infection which is endemic to certain parts of southeast Asia and China (4, 6, 7, 21). The first natural infection in humans was described in 1973 in a man suffering from Hodgkin's disease who had travelled to southeast Asia (5). Only 21 further cases were reported during the next 15 years (4, 9), most of which had no evidence of underlying impaired immunity. With the increasing prevalence of human immunodeficiency virus (HIV) infections in Thailand, Penicillium marneffei has emerged as a major opportunistic infection in AIDS patients (8, 19, 21). The common clinical manifestations of penicilliosis include fever, anemia, leukopenia, weight loss, diarrhea, hepatosplenomegaly, generalized lymphadenopathy, cough, and characteristic molluscum contagiosum-like lesions, predominantly on the face and trunk (4, 8, 19, 20, 21). The presentation may mimic tuberculosis, melioidosis, leishmaniasis, and other AIDS-related opportunistic infections, such as histoplasmosis and cryptococcosis (6, 8, 14, 21, 26). A presumptive diagnosis of penicilliosis can be made by finding characteristic yeast cells in smears of skin lesions, blood, bone marrow, or lymph nodes, but these may be confused easily with those of Histoplasma capsulatum and, occasionally, Cryptococcus neoformans or Leishmania sp. Definitive diagnosis relies upon the identification or isolation of P. marneffei in clinical specimens. However, conventional culture usually takes 3 days. Histological recognition of the pathogen (12, 15) is relatively straightforward, although the septa which distinguish P. marneffei from H. capsulatum may not always be seen. Identification of by means of an immunohistochemical approach (2) and exoantigen tests (7, 11, 17) is specific; however, these tests are also time-consuming and are not generally available. Rapid diagnosis is important, because disseminated P. marneffei infection has a high mortality, and effective antifungal treatments are available (7, 8, 18, 21).

A number of serological diagnostic tests have been developed for the detection of antibody to P. marneffei. These include an immunodiffusion test (12, 13, 23) and use of an indirect fluorescent antibody technique (25). We report the development and prospective evaluation of an enzyme-linked immunosorbent assay (ELISA) for the detection of P. marneffei antigen in urine, using a fluorescein isothiocyanate (FITC)-anti-FITC amplification system, in an area of northeastern Thailand in which penicilliosis is endemic.

	MATERIALS AND METHODS

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Patients. The study was conducted between June 1995 and November 1997. Adult patients with suspected or confirmed penicilliosis admitted to Sappasitprasong Hospital, Ubon Ratchathani, northeastern Thailand, were included in the study. All patients were seen by one of the study team. Full clinical details were recorded on a standard form. Routine hematological and biochemical tests were performed, and HIV antibody was measured when indicated with the ELISA. As part of the routine diagnostic workup, blood (15 ml), urine, and where appropriate, lymph node biopsy or liver aspirate specimens were collected for bacterial and fungal culture. Smears were made from any suspicious skin lesions or aspirates, and were then fixed on a glass slide and stained with Gram and Wright's stains. Throat and skin lesion swabs were also collected. All specimens were plated on Sabouraud's medium (with added chloramphenicol) and cultured at 30°C in air for up to 3 weeks.

Antigen preparation. A stock culture of P. marneffei (a clinical isolate from a patient in Ubon Ratchathani) was maintained on horse blood agar (HBA) at 37°C for several days. Fission-form arthroconidia (yeast-like cells) of P. marneffei were grown in 50 ml of brain heart infusion broth (BHIB) at 37°C for 2 weeks while being rotated on a rotary shaker at 150 rpm. The culture was checked weekly for the degree of turbidity and microscopic morphology. After 2 weeks of incubation, the culture was centrifuged at 2,900 × g for 10 min. The cell pellet was washed, resuspended in 10% formal saline solution to the original volume, and then left overnight at room temperature in order to kill the organisms. After repeat centrifugation, the cell pellet was washed, resuspended in normal saline, and adjusted to approximately 2 × 10⁸ cells/ml. After appropriate sterility checks, this was used as the immunogen for immunizing rabbits or as the control antigen for the ELISA.

Anti-P. marneffei IgG preparation. Hyperimmune sera against P. marneffei were prepared by injecting three female New Zealand White rabbits subcutaneously in the dorsal area with an emulsion consisting of 1 ml of 2 × 10⁸ cells/ml of killed-whole fission arthroconidia of P. marneffei and 2 ml of Freund's incomplete adjuvant, at weekly intervals for 3 weeks. One week after the third injection, the rabbits were injected intravenously with 0.5 ml of 5 × 10⁶ cells of killed-whole fission arthroconidia of P. marneffei per ml every 3 to 4 days for a further 2 weeks. Three days after the final injection, each rabbit was bled, and the serum was collected and pooled. This serum was tested for antibody against killed whole-fission arthroconidia of P. marneffei by using an immunodiffusion (ID) test similar to that described by Sekhon et al. (17). A single broad band was produced both before and after pooling the serum samples. The purified IgG fraction of the pooled immune serum was obtained by precipitation with 35% saturated ammonium sulfate and followed by fractionation by protein A-Sepharose CL-4B chromatography (Pharmacia, Uppsala, Sweden) by standard methods. The concentration of protein in the purified preparation was estimated by measuring the optical density at 280 nm.

Anti-P. marneffei IgG-FITC conjugate. FITC-labeled antibody was prepared by the method of Samual and others (16). Briefly, FITC (5 mg/ml in dry absolute ethanol) was added at a molar ratio of 20:1 to a stirred preparation of purified anti-P. marneffei IgG, diluted in 0.1 M carbonate buffer, containing 0.5 M NaCl (pH 9.2) in the dark at room temperature. The reaction was allowed to continue for a further 60 min, and then the anti-P. marneffei IgG-FITC was separated from free FITC by gel filtration through a Sephadex G-25 M PD-10 column (Pharmacia) preblocked with 1% bovine serum albumin, and equilibrated with phosphate-buffered saline (PBS). Fractions containing conjugate were pooled and stored at 4°C in PBS (33% [vol/vol]) containing 0.02% merthiolate.

Urinary antigen ELISA. Flat-bottom microtiter plates (Falcon 3912 Microtest III; Becton Dickinson, Oxnard, Calif.) were coated with capture antibody by adding 100 µl of purified rabbit anti-P. marneffei IgG (10 mg/ml) in PBS (pH 7.2) containing 0.02% (wt/vol) merthiolate to each well. The plates were incubated at 4°C for 48 h, and the wells were then washed three times with PBS containing 0.1% (vol/vol) Tween 20 (PBS-Tween).

Statistical analysis. Data were analyzed by using SPSS for Windows, version 6.1 (SPSS, Inc., Chicago, Ill.) computer software. Continuous variables with a nonnormal distribution were transformed. The comparability between data from each group of patients was assessed by one-way analysis of variance and Tukey's significant difference test or the Kruskal-Wallis one-way analysis of variance and Mann-Whitney U test, as appropriate. At each ELISA cutoff titer, the sensitivity (proportion of positives correctly identified by the test) and the specificity (proportion of negatives correctly identified by the test) were calculated. A receiver operating characteristic curve was then constructed by plotting sensitivity against (1  specificity) at each value (1).

	RESULTS

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Preliminary evaluation. Broth cultures of C. albicans, C. kefyr, C. neoformans var. neoformans, C. neoformans var. gattii, P. griseofulvum, P. chrysogenum, P. notatum, A. terreus, A. fumigatus, A. flavus, H. capsulatum var. capsulatum, and T. beigelii were nonreactive in the ELISA, even at cell concentrations of 10⁷ cells/ml. All of the clinical strains of P. marneffei (both fission and hyphal forms) were reactive down to concentrations of 100 yeast cells/ml. Bacterial strains were all nonreactive, except for Staphylococcus aureus (10⁸ CFU/liter), which was reactive only when undiluted.

Diagnostic sensitivity and specificity. Urine samples from 33 HIV-seropositive adult Thai patients with culture-confirmed P. marneffei infection were collected on admission. Urine samples from 248 patients with other diagnoses were also tested. These included 34 urine samples from HIV-seropositive patients with fungal infections other than penicilliosis. Of these, 31 were from patients with culture-confirmed cryptococcosis, 1 was from a patient with culture-confirmed histoplasmosis, and 2 were from patients with culture-confirmed candidiasis. The remaining patient samples were from 168 patients with culture-confirmed melioidosis, 12 from patients with septicemia due to other bacterial species, 7 from patients with other bacterial infections, and 27 from culture-negative patients (who were being screened for melioidosis as part of another study). All patients in the control groups mentioned above were admitted to Sappasitprasong Hospital during the same period as the penicilliosis patients. They had demographic characteristics similar to those of the penicilliosis patients. Fifty-two urine samples from healthy volunteers living in Ubon Ratchathani also served as negative controls, and 3 were used for the calculation of the ELISA standard deviations.

View larger version (16K): [in this window] [in a new window]   FIG. 1.   P. marneffei antigen titers in the urine collected on admission from 33 patients with penicilliosis and 300 control subjects and measured by ELISA. Group A (shaded circles) represents patients with culture-confirmed P. marneffei infection, group B had other fungal infections, group C had melioidosis, group D had other causes of bacterial septicemia, group E had other bacterial infections, group F had negative cultures, and group G were healthy controls. The triangles represent five patients, and the circles each represent one patient.

Optimum cutoff titer. The sensitivity and specificity of the ELISA in the diagnosis of penicilliosis are summarized in Table 2. Progressive dilution of urine samples reduced the sensitivity of the test, but the specificity increased to 100%. In order to achieve the best cutoff titer, a receiver-operating curve was used to assess the ability of the test to correctly identify patients with penicilliosis. This suggested that the best cutoff titer (i.e., the point that maximized the sum of the sensitivity and specificity) was at 1:40. At this cutoff titer, the ELISA was 97% sensitive and 98% specific (positive predictive value, 84.2%; negative predictive value, 99.7%). Repeated testing of a single sample with this initial titer gave values of 1:40 and 1:80. At a cutoff titer of 1:320, the specificity rose to 99%, but the sensitivity fell to 90% (positive predictive value, 91.3%; negative predictive value, 90.5%).

	DISCUSSION

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Penicilliosis is now recognized as one of the most important opportunistic infections in AIDS patients in Thailand. It is the fourth or fifth most common infection in this group of patients. Although in many cases, the diagnosis is readily made from microscopic examination of skin lesion smears, some patients do not have dermatological manifestations of the infection. In others, there may be confusion with histoplasmosis or disseminated cryptococcosis. Thus a rapid diagnostic or confirmatory test would be of clinical value and would direct appropriate antifungal therapy.

Yuen and colleagues (25) have developed an indirect immunofluorescence test to detect antibody in serum from patients infected with P. marneffei. All 78 healthy controls and 95 patients with fever from other causes had IgG titers of <1:40. Although there were only eight patients with P. marneffei infection in the series, all had IgG titers 160, but none had demonstrable IgM. Thus there was 100% sensitivity for this antibody test in this small series, although the study was performed in an area of low endemicity (Hong Kong) and included only two patients with other fungal infections (cryptococcosis). In an area of high endemicity, such as northern Thailand, background IgG seroprevalence could affect the specificity of the indirect fluorescent antibody IFA test.

Recently a specific 38-kilodalton antigen has been used to detect antibody to P. marneffei in HIV-seropositive patients in Thailand (3). Antibody was detected by immunoblotting in 30 (46%) of 65 patients with penicilliosis. In patients from an area in which P. marneffei is endemic, antibody was also found in 17 (25%) of 67 patients with cryptococcosis or candidiasis and in 45 (17%) of 262 asymptomatic HIV-positive individuals, but only 1 of 60 healthy controls. Thus, the specificity and usefulness of antibody tests for the diagnosis of penicilliosis in endemic areas remain uncertain. Other antigens from P. marneffei have been purified (10); one of these, a 61-kDa antigen, was recognized by sera from 18 of 21 (86%) P. marneffei-infected patients, but further evaluation of this in diagnostic tests is required.

Detection of P. marneffei antigen indicates active infection. However, it is known that there is some cross-reactivity between A. fumigatus and P. marneffei antigens, because antibody to A. fumigatus galactomannan reacts with P. marneffei in a latex agglutination test (22) and on immunohistochemical staining (2). A urinary antigen detection test developed for diagnosis of H. capsulatum var. capsulatum infection, using a rabbit IgG, has been reported to give positive results in 17 of 18 confirmed penicilliosis patients (24). Also, during the development of fluorescent-antibody tests for the tissue form of P. marneffei, Kaufman et al. (12) reported that the rabbit antiglobulin reacted with the yeast form of H. capsulatum but not with the hyphal form or the hyphal forms of A. flavus, A. fumigatus, and H. capsulatum or with Candida albicans, C. glabrata, or C. neoformans. Prior adsorption of the antiglobulin with yeast-form H. capsulatum could overcome this cross-reaction. These findings are consistent with those of Sekhon et al. (17), who reported no reactivity when rabbit antisera to mycelial elements of P. marneffei were tested with the exoantigens of eight monomorphic species of Penicillium or with hyphal antigens of Aspergillus spp. in the immunodiffusion test. Furthermore, Kaufman et al. (13) have developed an immunodiffusion test and a latex agglutination test to detect serum antigen. Both tests used rabbit antiserum raised against a culture filtrate of fission arthroconidia of P. marneffei which had the same antigens as those reported by Kaufman et al. (12). The tests were evaluated by using a small number of human sera. Serum antigen was detected by latex agglutination in 13 (76%) of 17 infected patients and by immunodiffusion in 10 (60%) patients. Antigen was not detected in serum samples from 15 normal Thai controls and six patients with cryptococcosis. P. marneffei antigen was also found in the urine from two infected patients, but not in six urine specimens containing Histoplasma antigen (13).

The polyclonal rabbit antiserum used in this study provides a highly sensitive and specific method for the diagnosis of penicilliosis in this area of endemicity. Of the 33 penicilliosis patients, 1 had detectable antigen only in neat urine (this patient had coinfection with C. neoformans) and a further 2 had titers of 1:40, while of the remaining 30 patients, 28 had titers of 1:2,560 or greater. Both of the patients with titers of 1:40 had very scanty skin lesions. One of these patients and the patient whose urine was positive only when undiluted had presented with disseminated cryptococcal infections. Because four of the six patients with false-positive antigen titers of >1:40 had cryptococcal infections, use of this cutoff titer alone for diagnosis would have lead to incorrect prescription of antifungal drugs in only two cases. Furthermore, these four patients were all HIV positive, and we cannot exclude the possibility that they were also infected with P. marneffei, although we were unable to culture it from suitable specimens. Of the other two patients with false-positive results, one was also HIV positive and had a Salmonella septicemia (titer, 1:5,120). This patient died shortly after blood cultures were collected and before other samples could be collected, so we cannot rule out coexisting penicillosis. The other patient (HIV test not done) was culture negative from blood and cerebrospinal fluid, but a coliform was grown from urine (titer, 1:160). This is not an area where leishmaniasis is prevalent, and so we cannot comment on test results for patients with this infection.

This antigen detection test should prove useful in diagnosis of P. marneffei infection and may be modifiable to a simple dot blot or latex agglutination form. The antigens recognized by the polyclonal antisera should now be characterized. The applicability of the test to serodiagnosis and the value of serial antigen detection in monitoring the response to treatment are currently being evaluated.