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Clinical and Vaccine Immunology, December 2007, p. 1592-1595, Vol. 14, No. 12
1071-412X/07/$08.00+0     doi:10.1128/CVI.00313-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Use of a Newly Developed β-Mercaptoethanol Enzyme-Linked Immunosorbent Assay To Diagnose Visceral Leishmaniasis in Patients in Eastern Sudan

Durria Mansour, Elfadil M. Abass, Mohamed el Mutasim, Abdelhafeiz Mahamoud, and Abdallah el Harith^*

Ahfad University for Women, P.O. Box 167, Omdurman, Sudan

Received 26 July 2007/ Returned for modification 12 September 2007/ Accepted 2 October 2007

Top ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 
Corroboration of serology results is essential for restricting the risk of inappropriate antileishmanial prescription. A direct agglutination test (DAT) and a recently developed β-mercaptoethanol-modified enzyme-linked immunosorbent assay (β-ME ELISA) based on the use of antigen prepared as described for the DAT were applied to 416 sera from two Sudanese populations with and without clinical evidence of visceral leishmaniasis (VL). Of 285 sera with the lowest antileishmanial DAT titers (1:100 to 1:1,600), 270 (94.7%) scored comparable minimum β-ME ELISA absorbance values (0.1 to 0.26). In 117 sera that demonstrated the highest DAT titers (1:12,800 to 1:25,600), 86 (73.5%) scored maximum (0.81 to 1.35) and 30 (25.6%) medium (0.27 to 0.80) β-ME ELISA absorbance values. VL diagnosis was established for 142 (44.1%) patients in the VL-symptomatic group (n = 322), based on positive microscopy for Leishmania donovani in lymph node aspirates or positive DAT (titer, 1:3,200). Of the 125 sera from the symptomatic patients for whom microscopy was positive for VL, 111 (88.8%) had comparable positive DAT and β-ME ELISA readings. In all 17 sera from the symptomatic DAT-positive patients for whom leishmaniasis was not established by microscopy but who responded favorably to antileishmanial therapy, absorbance values (0.27) indicative of VL were obtained by β-ME ELISA. Of 197 symptomatic patients for whom microscopy was negative for VL, 172 (87.3%) tested negative in β-ME ELISA and 180 (91.4%) in DAT. Based on the high reliability demonstrated here for VL detection, β-ME ELISA fulfills the requirement of confirming DAT results in patients manifesting suspected VL.

Top ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 
A prerequisite for sustainable control of visceral leishmaniasis (VL) in major areas of endemicity is the transfer of the necessary knowledge for reproducing established diagnostic tests. Although in several studies conducted in Sudan, properties of various imported tests were intensively evaluated, no measure regarding their long-term availability was addressed (2, 10, 11-14, 16).

At Ahfad University for Women (Omdurman, Sudan), direct agglutination tests (DAT) were successfully produced (7-9) through provision of modest laboratory facilities and training of medical personnel. National and international evaluations of the DAT produced in Sudan revealed excellent reliability for VL detection in both confirmed and unconfirmed cases in which patients responded favorably to antileishmanial therapy (9). However, despite the reports of high DAT reliability for VL detection, the decision to administer antileishmanial agents in unconfirmed cases should be adequately supported to avoid unnecessary health hazards.

By combining the use of a β-mercaptoethanol-modified antigen similar to that used in the DAT and an anti-human immunoglobulin G (IgG) conjugate for targeting specific IgG antibodies, a hybrid enzyme-linked immunosorbent assay (β-ME ELISA) was developed and successfully evaluated in a panel of reference VL and non-VL sera (1). The purpose of this study was to determine the reliability of the β-ME ELISA for detecting VL in patients suspected of having the disease presenting at a rural hospital in eastern Sudan.

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Study area and population. Three hundred twenty-two individuals suspected of having VL were received at Doka rural hospital during September 2004 to August 2006. Aside from fever (duration of 2 weeks), splenomegaly and lymphadenopathy were the most common manifestations in that group of patients. At our request, 56 other subjects residing in or around the same area and having no apparent manifestation or history of VL reported to the hospital and agreed to join the study as a healthy group from an area of endemicity. The necessary permission to conduct the study was granted by the Research Directorate, Federal Ministry of Health (Khartoum, Sudan).

VL diagnosis. Blood for serum was collected from all patients with suspected VL (n = 322) and the healthy subjects from the area of endemicity (n = 56). As routine diagnostic procedure, inguinal lymph specimens were collected from all patients with suspected VL. The aspirated lymph specimens were smeared onto glass slides and left to air dry. After methanol fixation, specimens were stained with Giemsa and examined under a microscope for amastigotes. Small portions of the sera collected from the patients with suspected VL and the healthy subjects were directly tested in the DAT (Doka rural hospital) by standard procedures described in detail previously (5, 6, 9). The remaining portions, designated for testing with the β-ME ELISA, were stored at –20°C until transportation to the central laboratory in Omdurman.

VL diagnosis was established either by demonstration of amastigotes in the Giemsa-stained lymph smears or by establishing titers of 1:3,200 in the DAT combined with positive disease presentation (15). Patients thus diagnosed with VL were then put on a 30-day treatment course with sodium stibogluconate (Pentostam; Albet-Davis). Patients determined not to have VL on the basis of microscopy or DAT results were referred to the district hospital in Gedarif for further investigation.

For comparison with the population from the area of endemicity, blood for serum was collected from 38 healthy female medical students (Khartoum state) who voluntarily agreed to serve as a control group. All serum samples were stored at –20°C until required.

β-ME ELISA. The antigen processing for β-ME ELISA was carried out as described for DAT with the exception of a Coomassie brilliant blue staining step (1). Following β-ME treatment and repeated washing in citrate saline solution, promastigotes were fixed as a stock suspension (1.5 x 10⁸/ml) in a 1.2% (vol/vol) formaldehyde citrate-saline solution. A working antigen promastigote concentration of 2.5 x 10⁷/ml versus respective serum and goat anti-human IgG peroxidase conjugate (Jackson Immunoresearch Laboratories, Inc.) dilutions of 1:12,800 and 1:100,000 was employed. Sera were assayed in duplicate along with appropriate negative and positive controls. The reaction was measured 15 min after addition of the substrate (5-aminosalicylic acid), at a 450-nm wavelength on a Titertek Multiscan. β-ME ELISA absorbance values of 0.27 were considered indicative of VL infection (1).

Supporting serological tests. The antigen for the urea-improved version of DAT was processed as described elsewhere (6). In order to confirm positive results obtained with β-ME ELISA in cases where microscopy was negative for VL, the urea-improved DAT and two commercially available VL diagnostic tests, namely, Leish-Kit (Lyopharma, Bilthoven, The Netherlands) and the rK39 strip test (DiaMed-AG, Cressier sur Morat, Switzerland), were applied. The urea-improved DAT was carried out as reported by el Harith et al. (6), and the Leish-Kit and rK39 strip test were used as instructed by the respective manufacturers.

Data analysis. For both β-ME ELISA and DAT, sensitivity was defined as the percentage of disease-positive patients with a positive test result {[true positives/(true positives + false negatives)] x 100}, and specificity was the percentage of the disease-negative individuals with a negative test result {[true negative/(false positive + true negative)] x 100}.

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Table 1 presents the distribution of anti-Leishmania antibodies as measured by β-ME ELISA and DAT in the mixed study population of patients with suspected VL, healthy individuals from the area of endemicity, and healthy individuals from other areas. Of the 285 individuals with DAT titers in the lowest range (1:100 to 1:1,600), 270 (94.7%) had comparable low absorbance values (0.1 to 0.26) in the β-ME ELISA. Among the 117 whose samples reacted at the highest DAT titer range (1:12,800 to 1:25,600), 86 (73.5%) also had high β-ME ELISA absorbance values (0.81 to 1.35). Besides 128 individuals identified as positive by both DAT (116 with titers of 1:12,800 to 1:25,600 and 12 at 1:3,200 to 1:6,400) and β-ME ELISA (87 at 0.81 to 1.35 and 41 at 0.27 to 0.80), 15 (3.6%) others tested positive, with absorbance values ranging from 0.27 to 0.80 in the latter test. All 142 VL patients diagnosed on the basis of microscopy or DAT (titers, 1:3,200) responded favorably to antileishmanial therapy. Of the 125 treated exclusively on the basis of positive microscopy, 115 (92.0%) had β-ME ELISA readings (0.27) indicative of VL (Table 2). β-ME ELISA absorbance values indicative of VL (0.27) were recorded for all 17 suspected VL patients who had not been identified by microscopy but were identified by DAT as having VL and responded favorably to antileishmanial therapy (Table 2). Therefore, based on positive responses to specific antileishmanial therapy rather than parasite demonstration, a sensitivity of 93.0% (132/142 x 100%) was calculated for β-ME ELISA and a sensitivity of 92.3% (131/142 x 100%) was calculated for DAT. Accordingly, respective specificity levels of 95.6% (172/180 x 100%) and 100% (180/180 x 100%) were established for the two tests with this group of patients with suspected VL.

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TABLE 1. Distribution of Leishmania antibody readings in a Sudanese study population comprising patients with suspected VL, healthy individuals from areas of endemicity, and controls from other areas

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TABLE 2. Comparison of β-ME ELISA results with the outcome of lymph node aspiration and DAT in 322 patients with suspected VL

In addition to the 17 VL cases that were successfully diagnosed by DAT in Doka rural hospital and thereafter by β-ME ELISA in the central laboratory (Omdurman), 8 more patients with suspected VL tested positive at the 0.27-to-0.54 absorbance range in the latter test (Table 2). In none of those eight were titers of >1:1,600 obtained with either the standard or urea-improved DAT; positive readings for two of them, however, were obtained with the rK39 strip test and/or Leish-Kit (Table 3).

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TABLE 3. Differences in readings obtained with β-ME ELISA, DAT, and the rK39 strip test for eight patients with suspected VL and negative microscopy results for L. donovania

Top ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 
Given the potent toxicity involved, the decision to prescribe antileishmanial agents for unconfirmed VL cases in the Sudan is a difficult one. This problem is further complicated by the high prevalence of infections that bear clinical resemblance to VL, such as malaria, tuberculosis, brucellosis, and typhoid. Postponing or withholding treatment in such cases could increase mortality and VL transmission rates in these already affected areas.

Since the establishment of DAT production in our laboratory, hundreds of patients with unconfirmed VL have been successfully diagnosed and treated (7, 9). Most challenging in this category, however, were cases in which the patient had a high negative or low positive DAT titer (1:800 to 1:3,200). Reliable diagnosis of VL in this group is therefore dependent on the availability of a supporting test(s).

In the present study, concordant β-ME ELISA and DAT results were obtained for 89.5% of the VL-seropositive patients and in as many as 94.7% of the seronegative patients. Also highly promising in this study were the sensitivities (93.0% or 92.3%) demonstrated by the two tests for diagnosing VL; 132 cases were identified by β-ME ELISA and 131 by DAT. Of the 114 VL cases confirmed on the basis of microscopy in which DAT was also positive, 111 gave positive β-ME ELISA readings (97.4% concordance with DAT). Both tests showed superiority over microscopy in that they detected VL in 17 more patients. Had microscopy been used as the sole criterion for diagnosis in this study, all 17 patients would have been denied VL treatment.

The results obtained with β-ME ELISA in this field study confirmed results obtained previously at the laboratory level, where, in addition to being used for VL, it was compared to the DAT for testing sera from patients with tuberculosis, leukemia, and African trypanosomiasis (1). However, earlier results obtained with an IgG ELISA where the water-soluble fraction of Leishmania donovani promastigotes was used as the antigen (4) showed that it compared less favorably to the DAT. At a slightly higher cutoff absorbance value (0.28) than that used here, 10% to 20% of Kenyan patients who had lived in the district of Baringo (Kenya), where VL is endemic, and who had suffered from malaria or brucellosis gave positive ELISA readings. Consistent with DAT results, though, were those obtained with an improved ELISA utilizing recombinant Leishmania antigen (rK39) in a Sudanese VL population from the eastern state (17). Efforts to further simplify VL diagnosis that included application of the same antigen to a strip device failed to match those of the DAT in two VL patient groups from an area in the Sudan where VL is endemic or epidemic (17). Further evaluation of the rK39 strip test in eastern and southern Sudan revealed significantly lower sensitivity (90.0%) and specificity (70.0%) than those reported for the DAT (respectively, 99% and 85%) (12, 14). In our opinion, the high specificity demonstrated for β-ME ELISA and DAT in this and a previous study (1) can be attributed only to the favorable effect brought about by β-ME on the promastigote membrane, whereby cross-reacting molecules were drastically reduced to elicit reaction against non-VL sera. However, as has been found with other versions of the ELISA, determination of the cutoff level in this β-ME ELISA can be influenced by the level of VL endemicity in the study area, the causative Leishmania subspecies involved, and the reagent lot employed.

The positive readings obtained with β-ME ELISA in eight patients with unconfirmed but strongly suspected VL suggest possible exposure to L. donovani. Early or subclinical VL infection cannot be excluded with certainty, since in this β-ME ELISA no antibodies other than those of the IgG class were targeted, and amastigotes may have escaped microscopic detection, possibly because they were scarce in the lymph aspirates. The positive readings obtained in samples from two of those patients with the rK39-strip test and/or Leish-Kit (Table 3) provided further evidence of this possibility. Notwithstanding the discrepancy observed here between DAT and the two commercial tests, recent analysis of data collected from several studies evidenced comparable diagnostic reliability for VL regardless of the parasitological outcome (3).

Plans for enhancing β-ME ELISA performance to provide early warning of VL include further modification for detecting antibody response in the IgM serum fraction of patients with suspected VL.

 
We thank Gasim Badri, president of Ahfad University, Farouk A/Aziz, dean of the School of Medicine, and Abubaker Uro, head of the Ahfad Centre for Science and Technology, for their invaluable support and encouragement. The efforts of M. Mukhtar and W. el Amin, Institute of Endemic Diseases, University of Khartoum, for cryopreservation and maintenance of the Leishmania strain are greatly appreciated.

This investigation received technical and financial support (grant SGS 05/146) from the joint WHO Eastern Mediterranean Region (EMRO), Division of Communicable Diseases (DCD), and the WHO Special Program for Research and Training in Tropical Diseases (TDR): EMRO/TDR Small Grant Scheme for Operational Research in Tropical and Other Communicable Diseases.

 
* Corresponding author. Present address: Wijngaard 155, 8212 CJ Lelystad, The Netherlands. Phone and fax: 31 320 235 229. E-mail: harith17{at}yahoo.com

Published ahead of print on 17 October 2007.

Present address: Laboratory Department, Aljouf College of Health Sciences for Boys, Sakaka, Aljouf, Kingdom of Saudi Arabia.

Top ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 

1
1. Abass, E. M., D. Mansour, M. el Mutasim, M. Hussein, and A. el Harith 2006. β-Mercaptoethanol-modified ELISA for diagnosis of visceral leishmaniasis. J. Med. Microbiol. 55:1193-1196.[Abstract/Free Full Text]
2
2. Boelaert, M., S. H. El Safi, D. Jacquet, A. de Muynck, P. van der Stuyft, and D. Le Ray. 1999. Operational validation of the direct agglutination test for diagnosis of visceral leishmaniasis. Am. J. Trop. Med. Hyg. 60:129-134.[Abstract]
3
3. Chappius, F., A. Rijal, J. Menten, and M. Boelaert. 2006. A meta-analysis of the diagnostic performance of the direct agglutination test and rK39 dipstick for visceral leishmaniasis. Br. Med. J. 333:723-726.[Abstract/Free Full Text]
4
4. el Harith, A., A. H. J. Kolk, P. A. Kager, J. Leeuwenburg, F. J. Faber, R. Muigai, S. Kiugu, and J. J. Laarman. 1987. Evaluation of a newly developed direct agglutination test (DAT) for serodiagnosis and sero-epidemiological studies of visceral leishmaniasis: comparison with IFAT and ELISA. Trans. R. Soc. Trop. Med. Hyg. 81:603-606.[CrossRef][Medline]
5
5. el Harith, A., A. H. J. Kolk, J. Leeuwenburg, R. Muigai, E. Huigen, T. Jelsma, and P. A. Kager. 1988. Improvement of a direct agglutination test for field studies of visceral leishmaniasis. J. Clin. Microbiol. 26:1321-1325.[Abstract/Free Full Text]
6
6. el Harith, A., S. Chowdhury, M. Al-Masum, S. J. Semiao-Santos, E. Karim, S. H. El-Safi, and I. Haque. 1995. Evaluation of cleaving agents other than trypsin in direct agglutination test for further improving diagnosis of visceral leishmaniasis. J. Clin. Microbiol. 33:1984-1988.[Abstract]
7
7. el Harith, A., M. El Mutasim, D. Mansour, E. F. Mustafa, I. Shammat, I. Gilis, and T. van Gool. 2002. National and international evaluation of in-Sudan produced direct agglutination test for visceral leishmaniasis. Sudan Med. J. 40:3-11.
8
8. el Harith, A., M. el Mutasim, D. Mansour, E. F. Mustafa, and A. Arvidson. 2003. Use of glycerol as alternative to freeze-drying for long-term preservation of antigen for the direct agglutination test. Trop. Med. Int. Health 8:1025-1029.[CrossRef][Medline]
9
9. el Mutasim, M., D. Mansour, E. M. Abass, W. Hassan, and A. el Harith. 2006. Evaluation of a glycerol-preserved antigen in the direct agglutination test for diagnosis of visceral leishmaniasis in eastern Sudan. J. Med. Microbiol. 55:1343-1347.[Abstract/Free Full Text]
10
10. El-Safi, S. H., A. Abdel-Haleem, A. Hammad, I. El-Basha, A. Omer, H. G. Kareem, M. Boelaert, M. Chance, and M. Hommel. 2003. Field evaluation of latex agglutination test for detecting urinary antigens in visceral leishmaniasis in Sudan. East Mediterranean Health J. 9:844-855.
11
11. Osman, O. F., P. A. Kager, and L. Oskam. 2000. Leishmaniasis in the Sudan: a literature review with emphasis on clinical aspects. Trop. Med. Int. Health 5:553-562.[CrossRef][Medline]
12
12. Ritmeijer, K., Y. Melaku, M. Mueller, S. Kipngetich, C. O'Keeffe, and R. N. Davidson. 2006. Evaluation of a new recombinant K39 rapid diagnostic test for Sudanese visceral leishmaniasis. Am. J. Trop. Med. Hyg. 74:76-80.[Abstract/Free Full Text]
13
13. Seaman, J., R. W. Ashford, J. Schorscher, and J. Dereure. 1992. Visceral leishmaniasis in Southern Sudan: status of healthy villagers in epidemic conditions. Ann. Trop. Med. Parasitol. 86:481-486.[Medline]
14
14. Veeken, H., K. Ritmeijer, J. Seaman, and R. Davidson. 2003. Comparison of an rK39 dipstick rapid test with direct agglutination test and splenic aspiration for the diagnosis of kala-azar in Sudan. Trop. Med. Int. Health 8:164-167.[CrossRef][Medline]
15
15. World Health Organization. 2004. Report of the Scientific Working Group meeting on leishmaniasis. TDR/SWG/04. http://www.who.int/tdr/publications/publications/pdf/swg_leish.pdf
16
16. Zijlstra, E. E., N. S. Daifalla, P. A. Kager, E. A. G. Khalil, A. M. El-Hassan, S. G. Reed, and H. W. Ghalib. 1998. rK39 enzyme-linked immunosorbent assay for diagnosis of Leishmania donovani infection. Clin. Diagn. Lab. Immunol. 5:717-720.[Medline]
17
17. Zijlstra, E. E., Y. Nur, P. Desjeux, E. A. G. Khalil, A. M. El-Hassan, and J. Groen. 2001. Diagnosing visceral leishmaniasis with the recombinant K39 strip test: experience from the Sudan. Trop. Med. Int. Health 6:108-113.[CrossRef][Medline]

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Clinical and Vaccine Immunology, December 2007, p. 1592-1595, Vol. 14, No. 12
1071-412X/07/$08.00+0     doi:10.1128/CVI.00313-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

This Article Abstract Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Reprints and Permissions Copyright Information Books from ASM Press MicrobeWorld Citing Articles Citing Articles via Google Scholar Google Scholar Articles by Mansour, D. Articles by el Harith, A. Search for Related Content PubMed PubMed Citation Articles by Mansour, D. Articles by el Harith, A.