Detection of Cryptosporidium parvum oocysts in calf fecal samples by direct immunofluorescence assay

Detecção de oocistos de Cryptosporidium parvum em amostras fecais de bezerros pela reação de imunofluorescência direta

FULL ARTICLE

Detection of Cryptosporidium parvum oocysts in calf fecal samples by direct immunofluorescence assay

Detecção de oocistos de Cryptosporidium parvum em amostras fecais de bezerros pela reação de imunofluorescência direta

Weslen Fabricio Pires Teixeira^I; Willian Marinho Dourado Coelho^II; Cáris Maroni Nunes^I; Marcelo Vasconcelos Meireles^I

^IFaculdade de Medicina Veterinária, Universidade Estadual Paulista – UNESP

^IIFaculdade de Ciências Agrárias e Veterinárias, Universidade Estadual Paulista – UNESP

^{Corresponding author}

ABSTRACT

The aim of this study was to produce a conjugate containing anti-Cryptosporidium parvum polyclonal antibodies and standardize a Direct Immunofluorescence Assay (DIF) for detecting C. parvum oocysts in fecal samples from calves. In order to obtain anti-C. parvum polyclonal antibodies, two New Zealand rabbits were immunized with a purified solution of C. parvum oocysts and Freund's adjuvant. Purification of the immunoglobulin G (IgG) fraction was performed by means of precipitation in ammonium sulfate and chromatography using a DEAE-cellulose column. The anti-C. parvum polyclonal antibody titer was determined by means of the enzyme-linked immunosorbent assay (ELISA). The rabbit anti-C. parvum IgG fraction was conjugated with fluorescein isothiocyanate and standardization of the DIF was performed using various dilutions of conjugate on slides positive for C. parvum oocysts. The cross-reactivity of the anti-C. parvum conjugate was tested using oocysts of Cryptosporidium serpentis, Cryptosporidium andersoni, Escherichia coli, Eimeria sp., and Candida sp. An anti-C. parvum conjugate was successfully produced, thus allowing standardization of DIF for detection of Cryptosporidium oocysts in fecal samples. Cross-reactivity of anti-C. parvum polyclonal antibodies with C. andersoni and C. serpentis was also observed.

Keywords: Direct immunofluorescence, oocysts, Cryptosporidium parvum, fecal samples, cattle.

RESUMO

O objetivo deste estudo foi produzir um conjugado contendo anticorpos policlonais anti-Cryptosporidium parvum e padronizar a Reação de Imunofluorescência Direta (RID), para detecção de oocistos de C. parvum em amostras fecais de bezerros. Para produção de anticorpos policlonais anti-C. parvum, dois coelhos da raça Nova Zelândia foram imunizados com uma solução purificada de oocistos de C. parvum e adjuvante de Freund. A purificação da fração de imunoglobulina G (IgG) foi realizada por meio de precipitação em sulfato de amônio e cromatografia em coluna de DEAE celulose. A titulação dos anticorpos policlonais anti-C. parvum foi determinada por meio de ensaio imunoenzimático (ELISA). A fração IgG de coelho anti-C. parvum foi conjugada com isotiocianato de fluoresceína, e a padronização da RID foi feita utilizando-se várias diluições do conjugado, em lâminas positivas para C. parvum. Foi pesquisada também a presença de reatividade cruzada do conjugado anti-C. parvum com C. serpentis, C. andersoni, Escherichia coli, Eimeria sp. e Candida sp.. A produção do conjugado anti-C. parvum foi bem sucedida, sendo possível a padronização da RID para detecção de oocistos em fezes. Foi também observada reatividade cruzada dos anticorpos policlonais anti-C. parvum, com C. andersoni e C. serpentis.

Palavras-chave: Imunofluorescência direta, oocistos, Cryptosporidium parvum, amostras fecais, bovinos.

Introduction

Cryptosporidiosis in neonate calves is generally caused by Cryptosporidium parvum, with reports of infections in which up to 6×10¹¹ oocysts per animal are eliminated during the first month of life (UGA et al., 2000). This represents a risk of transmission to other animals and also to humans, given that C. parvum presents high zoonotic potential (XIAO; FAYER, 2008).

The importance of C. parvum as an etiological agent for diarrhea, enteritis and mortality among calves, during their first weeks of life, has already been confirmed by several researchers (SANFORD; JOSEPHSON, 1982; HEINE et al., 1984; GARCIA; LIMA, 1994; SOUZA; LOPES, 1995; FEITOSA et al., 2008).

Among the techniques used to detect Cryptosporidium oocysts in fecal samples, the direct immunofluorescence assay (DIF) is prominent (FAYER et al., 2000; BIALEK et al., 2002; JEX et al., 2008). It has been recognized as presenting better sensitivity and specificity than shown by traditional staining techniques (ARROWOOD; STERLING, 1989; JOHNSTON et al., 2003).

Imported DIF kits using anti-C. parvum monoclonal antibodies labeled with fluorescein thiocyanate exist on the market (GRACZYK et al., 1996). However, the acquisition cost of these products makes it practically impossible to use them in routine laboratory analyses (ALLES et al., 1995; CARVALHO, 2009).

The aim of the present study was to produce a conjugate with anti-C. parvum polyclonal antibodies and standardize DIF for detecting C. parvum oocysts in fecal samples from calves.

Material and Methods

This study was approved by the Ethics Committee for Animal Use of the Dentistry School of UNESP, Araçatuba Campus, on October 10, 2008, under protocol number 2008-006645.

1. Production of anti-C. parvum polyclonal antibodies

Anti-C. parvum polyclonal antibodies were produced in two adult New Zealand rabbits (A and B), by means of an initial intradermal inoculation of a solution containing 3 × 10⁶ intact C. parvum oocysts and Freund's complete adjuvant, in proportions of 1:1. This was followed by intramuscular inoculation with 2 × 10⁶ oocysts and Freund's incomplete adjuvant, in proportions of 1:1, which was done three, six and eight weeks after the first inoculation (STIBBS; ONGERTH, 1986). The C. parvum oocysts used for the inoculations came from a feces sample from a calf on a dairy farm in the municipality of Araçatuba, state of São Paulo. The oocysts were subjected to the technique of centrifugation-sedimentation in water and ether (MELONI; THOMPSON, 1996), purification in a cesium chloride solution (ARROWOOD; DONALDSON, 1996) and quantification in a Neubauer chamber. The sediment was then stored at 4 ºC in 1% formalin at pH 7.6 (STIBBS; ONGERTH, 1986).

The Cryptosporidium species present in the inoculum was determined by means of microscopic analysis (morphology and morphometry) and by means of molecular classification using the nested polymerase chain reaction (PCR) to amplify 18S rRNA gene fragments (XIAO et al., 2000), with subsequent sequencing of the amplified fragments.

Five days after the last inoculation, the rabbits were anesthetized using acepromazine and sodium thiopental, and blood samples were collected by means of cardiac puncture. The serum was obtained by means of centrifugation of the blood samples at 1,500 rpm, for 5 minutes at 4 ºC, and was then stored at –20 ºC (STIBBS; ONGERTH, 1986).

To ascertain the anti-C. parvum antibody titers before and after oocyst inoculation, the indirect enzyme-linked immunosorbent assay (ELISA) was used. Two aliquots of 1 mL of serum from each rabbit were stored: one from the day of the first inoculation and the other five days after the last inoculation.

2. Indirect ELISA for rabbit anti-C. parvum antibody titers

The antigen used in ELISA was produced from 23 × 10⁶C. parvum oocysts that were purified in cesium chloride, diluted in PBS (pH 7.4) and sonicated in an ice bath for 10 cycles of ten seconds, with 20-second resting intervals between one cycle and the next. After protein assaying using the BCA® kit (Sigma, St Louis, USA), the antigen was used at a concentration of 10 µg.mL^–1.

The serum samples from the rabbits that were collected before and after oocyst inoculation were tested at proportions of 1:1,000 (serum/5% skimmed milk).

A conjugate composed of anti-rabbit IgG (whole molecule)-peroxidase antibody produced in goat (A6154®; Sigma, St Louis, USA) was used in proportion of 1:5,000 (conjugate/5% skimmed milk). After 20 minutes of addition of the substrate tetramethylbenzidine (00-2023®; Invitrogen, Carlsbad, USA), the enzymatic reaction was stopped with 1N HCl. The reactions were read using a microplate reader (Labsystems Multiskan EX), with a 450 nm filter.

The reactions were read using a microplate reader (Labsystems Multiskan EX), with a 450 nm filter.

3. Conjugate production

To produce the conjugate, serum from rabbit A was used. The gamma-globulin fraction was purified by means of precipitation using 35% ammonium sulfate (70% ammonium sulfate solution diluted in proportions of 1:1 with rabbit serum) and centrifugation at 7,000 g, for 30 minutes. The resultant sediment was diluted in 3 mL of 0.01M PBS (pH 7.2), placed on a dialysis membrane and immersed in 0.025M Tris-HCl buffer (pH 8.8) for 18 hours, in order to remove the excess ammonium sulfate (HERBERT et al., 1973).

The IgG fraction was obtained by means of ion-exchange chromatography in a column using DEAE-cellulose gel (CORTHIER et al., 1984), and protein assaying of the gamma-globulin fraction and IgG fraction was carried out using the BCA® kit (Sigma, St Louis, USA).

The reactivity of the anti-C. parvum IgG fraction was tested by means of indirect ELISA, in proportions of 1:400 (IgG/5% skimmed milk). After the reactivity of the IgG fraction against antigens of C. parvum had been proven, this fraction was conjugated with fluorescein isothiocyanate (Sigma, St Louis, USA), by means of diluting 15 mL of the IgG fraction from rabbit A in 3 mL of 0.5M carbonate-bicarbonate buffer (pH 9.5). To this solution, 1.46 mg of fluorescein isothiocyanate was added (0.02 mg for each mg of protein contained in the rabbit IgG sample), with incubation at 4 ºC, overnight.

Purification of the conjugated antibody was done in a Sephadex G25 gel column (Sigma, St Louis, USA), in the proportions of 1 cm of gel in the column for each 1 mL of conjugate sample.

The solution containing the conjugate was divided into aliquots of 2 mL in amber tubes and was frozen at –20 ºC.

4. Direct immunofluorescence assay

The slides used for DIF were firstly treated with polylysine (Sigma, St Louis, USA), diluted in the proportions of 1:20, in deionized water (ARROWOOD et al., 1991). To this, 25 µL of purified feces sample that was positive for C. parvum oocysts (conserved in 10% buffered formalin in the proportion of 1:3) was added. The sample drop was left to dry out completely at room temperature. Subsequently, 25 µL of anti-C. parvum conjugate was added at several dilutions (1:40, 1:80 and 1:100), in 0.01M PBS (pH 7.2) and 4'.6'-diamidine-2-phenylindole (DAPI) (50 µl of DAPI at 2 mg.mL^–1 to 50 mL of 0.01M PBS, pH 7.2), and the slide was incubated at 37 ºC for 30 minutes, in a damp chamber. At the end of the incubation, the sample was washed using 0.01M PBS (pH 7.2), and the slide mounting was completed using a cover slip over 25 µL of mounting buffer (90% glycerol in 0.01M PBS, pH 7.2; 0.1 mg.mL^–1 of p-phenylenediamine) (PLATT; MICHAEL, 1983).

The reaction was read under an Olympus BX-50 microscope with a 100 W mercury light bulb and the U-MWU2 filter (DAPI) and U-MWU2-B filter (fluorescein), at a magnification of 400×.

5. Determination of DIF specificity

Confirmation of the diagnosis obtained by means of DIF was achieved by means of microscopic examination using differential interference contrast (DIC) and staining with 4',6'-diamidine-2-phenylindole (DAPI) (SMITH et al., 2002).

Using the same DIF methodology as for C. parvum oocysts, the presence of cross-reactivity of anti-C. parvum IgG with Escherichia coli, Eimeria sp., Candida sp. and other species of Cryptosporidium (C. andersoni and C. serpentis) was investigated. The C. andersoni and C. serpentis oocysts were isolated, respectively, from fecal samples from a calf on a dairy farm in the municipality of Muritinga do Sul, state of São Paulo, and from a royal python (Python regius) from the city of São Paulo, state of São Paulo. These samples were subjected to the same purification and classification methods as used for the inoculum that was destined for production of anti-C. parvum polyclonal antibodies.

Results

The volumes of serum samples obtained from rabbits A and B were respectively 36 and 39 mL. The protein concentration and ELISA results from the gamma-globulin fraction and purified IgG fraction in a DEAE-cellulose column showed that rabbit A yielded greater production of antibodies than did rabbit B (Table 1).

Table 2 describes the results from ELISA performed on the rabbit serum collected before and after inoculation of C. parvum oocysts and on the purified IgG fraction in the DEAE-cellulose column.

The total volume of conjugate produced was 12 mL, and the proportions of 1:80 were used for the dilution. This dilution enabled the best results with regard to viewing the C. parvum oocysts.

The fluorescence observed in the C. parvum oocysts emanated mainly from their walls (Figure 1). In the DIF specificity test, the conjugate did not present any cross-reactivity with E. coli, Eimeria sp. or Candida sp. On the other hand, cross-reactivity was found with C. andersoni and C. serpentis.

Discussion

The volume of the IgG fraction from rabbit A was greater than that of rabbit B. This was because the peak elimination of IgG in the purification process for the gamma-globulin fraction of rabbit A was greater than that of rabbit B, thereby increasing the length of the procedure and resulting in greater dilution of the sample in 0.025M Tris-HCl buffer (pH 8.8), consequent to the greater protein concentration of the gamma-globulin fraction in rabbit A.

The inoculums through intradermal and intramuscular routes, with solution of intact C. parvum oocysts were performed with the aim of promoting production of antibodies against antigens that are present in the walls of the oocysts. This binding could be proven through DIF, in which it was observed that the fluorescence of the oocysts emanated from their walls. However, in the present study, the affinity of anti-C. parvum antibodies for the internal structures of the oocysts was not tested.

The conjugate was used at a dilution of 1:80, in PBS (pH 7.4), with good levels of fluorescence of oocysts, such that the fluorescence only diminished at the dilution of 1:100. Stibbs and Ongerth (1986) standardized the indirect immunofluorescence assay for detecting Cryptosporidium sp. oocysts in fecal samples from monkeys and humans, and they achieved the best results in relation to oocyst fluorescence at conjugate dilutions of 1:20, 1:40 and 1:60 in PBS (pH 7.6), with a considerable decrease at the dilution of 1:80.

The conjugate at the dilution of 1:80 made it possible to carry out DIF in duplicate, on 1.6 feces samples from calves, with a volume of only 1 µL. In other words, with 12 mL of anti-C. parvum conjugate produced from 15 mL of sample from the IgG fraction of rabbit A, it would be possible to carry out analyses in duplicate on 19, 200 samples. This would considerably decrease the cost of this procedure in comparison with the cost of using commercial kits.

The absence of cross-reactivity of the polyclonal antibodies used in this study, with other etiological agents, corroborates the results obtained by Graczyk et al. (1996). These authors investigated the specificity of the monoclonal antibody used in the Merifluor Cryptosporidium/Giardia® DIF kit (Meridian Diagnostics, Cincinnati, USA), for detecting Cryptosporidium, and did not observe any cross-reactivity with samples containing eggs from eight helminth species, three species of Eimeria, sporocysts of Sarcocystis cruzi and two isolates of Candida sp. These authors also tested for the presence of cross-reactivity with other species of Cryptosporidium (C. serpentis, C. meleagridis, C. wrairi, C. muris and C. muris-like) and observed cross-reactivity with all the species tested. These findings are similar to those of the present study, in which the conjugate presented cross-reactivity with C. serpentis and C. andersoni.

Stibbs and Ongerth (1986) did not observe any nonspecific binding of anti-Cryptosporidium sp. polyclonal antibodies, when tested against Candida albicans, Giardia lamblia, Entamoeba histolytica, Giardia sp., Entamoeba sp. and Blastocystis hominis. However, nonspecific binding of anti-Cryptosporidium antibodies occurred with oocysts of Eimeria sp. and Caryospora, which did not occur with any of the etiological agents tested in the present study.

Conclusions

An anti-C. parvum conjugate containing antibodies originating in a rabbit was successfully produced, thus making it possible to standardize DIF for detecting C. parvum oocysts in fecal samples.

No cross-reactivity was observed between the conjugate produced and Escherichia coli, Eimeria sp. and Candida sp.

The anti-C. parvum conjugate presented cross-reactivity with C. andersoni and C. serpentis, which enables its use for detecting oocysts from other Cryptosporidium species in fecal samples.

Acknowledgements

We would like to thank Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) for the following grants: financial support (2008/57380-1).

Received January 24, 2011

Accepted August 23, 2011

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Publication Dates

• Publication in this collection
  21 Dec 2011
• Date of issue
  Dec 2011

History

• Received
  24 Jan 2011
• Accepted
  23 Aug 2011