Detection of excretory Entamoeba histolytica DNA in the urine, and detection of E. histolytica DNA and lectin antigen in the liver abscess pus for the diagnosis of amoebic liver abscess

Background Amoebic liver abscess (ALA) and pyogenic liver abscesses (PLA) appear identical by ultrasound and other imaging techniques. Collection of blood or liver abscess pus for diagnosis of liver abscesses is an invasive procedure, and the procedure requires technical expertise and disposable syringes. Collection of urine is a noninvasive procedure. Therefore, there has been much interest shown towards the use of urine as an alternative clinical specimen for the diagnosis of some parasitic infections. Here, we report for the first time the detection of E. histolytica DNA excreted in the urine for diagnosis of the cases of ALA. Results E. histolytica DNA was detected in liver abscess pus specimen of 80.4% of ALA patients by a nested multiplex polymerase chain reaction (PCR) targeting 16S-like r RNA gene. The nested PCR detected E. histolytica DNA in all 37 (100%) liver abscess pus specimens collected prior to metronidazole treatment, but were detected in only 53 of 75 (70.6%) pus specimens collected after therapy with metronidazole. Similarly, the PCR detected E. histolytica DNA in 21 of 53 (39.6%) urine specimens of ALA patients. The test detected E. histolytica DNA in only 4 of 23 (17.4%) urine specimens collected prior to metronidazole treatment, but were detected in 17 of 30 (56.7%) urine specimens collected after treatment with metronidazole. The enzyme-linked immunosorbent assay (ELISA) for the detection of lectin E. histolytica antigen in the liver abscess pus showed a sensitivity of 50% and the indirect haemagglutination (IHA) test for detection of amoebic antibodies in the serum showed a sensitivity of 76.8% for the diagnosis of the ALA. Conclusion The present study for the first time shows that the kidney barrier in ALA patients is permeable to E. histolytica DNA molecule resulting in excretion of E. histolytica DNA in urine which can be detected by PCR. The study also shows that the PCR for detection of E. histolytica DNA in urine of patients with ALA can also be used as a prognostic marker to assess the course of the diseases following therapy by metronidazole. The detection of E. histolytica DNA in urine specimen of ALA patients provides a new approach for the diagnosis of ALA.


Background
Infection with Entamoeba histolytica, results in 34 million to 50 million symptomatic cases of amoebiasis worldwide each year, causing 40 to 100 thousand deaths annually [1]. Mortality from amoebiasis is mainly due to extraintestinal pathology, of which amoebic liver abscess (ALA) is the most common. If left untreated, ALA can rupture into neighboring tissue and spread to the brain and other organs via hematological route producing serious morbidity and mortality. It is difficult to differentiate clinically the ALA from pyogenic liver abscess (PLA) as well as from other space occupying lesions of liver such as hydatid cyst and liver hepatoma [2,3].
Imaging techniques like ultrasound, computed tomography, and magnetic resonance although are highly sensitive to detect abscesses in the liver of varied aetiology, however fail to distinguish specifically ALA from that of PLA. Less than one third of patients with ALA have active diarrhea [3]. Hence, stool microscopy and stool antigen detection is not very helpful for diagnosis of ALA. In fact less than only 10% of ALA patients have identifiable E. histolytica in stool specimens [4].
Laboratory diagnosis of ALA is usually established by conventional antibody-based serological tests. Nevertheless, the main disadvantage with antibody detection is that serum antibody levels in individuals living in endemic areas, continues to remain positive even for years after infection with E. histolytica [5][6][7]. The demonstration of amoebic antibodies in the serum, therefore, fails to denote the amoebic infection whether it is recent or old. Furthermore, serum amoebic antibodies are not demonstrated in up to 10% of the patients with acute ALA [3].
The demonstration of E. histolytica trophozoite in liver abscess pus aspirates by microscopy confirms the diagnosis of ALA, but in best of the laboratories, the amoebic trophozoites can be demonstrated in only 15% of the liver pus [8]. Since the trophozoites of E. histolytica are found mainly in the periphery of the abscess diagnosis of ALA by culture of liver pus for E. histolytica is also unsatisfactory [9].
Demonstration of amoebic antigen in the liver pus is a recent approach for specific diagnosis of the ALA. A monoclonal antibody-based second generation TechLab enzyme-linked immunosorbent assay (ELISA) kit (Blacksburg, Va.) has been reported to be 78% sensitive for the detection of E. histolytica lectin antigen in the liver pus for the diagnosis of ALA in Dhaka, Bangladesh [10]. Studies conducted in various laboratories worldwide including ours have shown that polymerase chain reaction (PCR) is a sensitive and specific method for detecting Entamoeba DNA in stool samples and for differentiating the morphologically similar E. histolytica from Entamoeba dispar and Entamoeba moshkovskii [11][12][13][14][15][16][17][18][19]. However, only few studies using the PCR have been reported for the detection of Entamoeba DNA in liver abscess pus for the diagnosis of the ALA [20,21,9,10].
Collection of blood or liver abscess pus is an invasive procedure, and the procedures require technical expertise and disposable syringes [22]. The method if not carried out under stringent conditions is associated with the risk of acquiring needle-borne infections such as hepatitis B virus and human immunodeficiency virus (HIV). Therefore, of late much interest has been shown towards the use of urine as a specimen alternate to the blood for the diagnosis of some parasitic infections including malaria, schistisomiasis, kala-azar, cystic echinococcosis and neurocysticercosis [22]. Urinary antigen for cystic echinococcosis (CE) and neurocysticercosis has been reported for the first time from our laboratory at Jawaharlal Institute of Postgraduate Medical Education and Research (JIP-MER), Puducherry, India [23,24]. Our laboratory has developed for the first time a counter-current immunoelectrophoresis (CIEP) and co-agglutination (Co-A) to detect the hydatid antigen excreted in the urine for the diagnosis of CE [23,25], and Co-A to detect cysticercus antigen in the urine for the diagnosis of neurocysticercosis [24].
Detection of DNA in urine by PCR has been employed for the diagnosis of Toxoplasma gondii, Neisseria gonorrhoeae, Borrelia burgdorferi, Mycobacterium tuberculosis, Mycobacterium leprae and Chlamydia trachomatis infections [26][27][28][29][30]. Some studies have also shown that the kidney barrier in rodents and humans is permeable to DNA molecules large enough to be analyzed by standard genetic methodologies [31,32]. To the best of our knowledge till now there is no report available on detection of Entamoeba DNA in the urine for the diagnosis of ALA. In the present study, therefore for the first time, we have evaluated a nested multiplex PCR for detection of Entamoeba DNA excreted in the urine for the diagnsosis of ALA.

Results
The quantification of DNA in the liver abscess pus and urine specimen by Spectrophotometric analysis showed the DNA yield to be approximately 85 and 3 μg/ml respectively. The purity of DNA extract from liver abscess pus and urine specimens was found to be satisfactory as the value of ratio of readings at 260 nm and 280 nm (OD 260 / OD 280 ) was approximately 1.8-1.85.
The sequencing result of PCR product of E. histolytica from liver abscess pus and urine specimen showed 99% identities to the sequence deposited in GenBank, [accession number: X56991]. The result of assessment of competition of other non target DNA present in liver abscess pus (PLA pus negative for E. histolytica) and urine (negative control group) specimen with target DNA, showed expected amplification and no nonspecific amplification in nested multiplex PCR.
Estimation of minimum number of Entamoeba cells detectable by nested multiplex PCR showed that the detection limit of PCR was found to be approximately 15 E. histolytica cells as even 1.5 μl of template DNA from 1000 E. histolytica cells/100 μl of Tris-ethylenediamine tetraacetic acid (EDTA) (TE) buffer produced a positive signal.
The IHA test was positive for serum antibodies in the serum of 86 (61.9%) of 139 patients provisionally diagnosed as ALA. The test was positive in a higher number of serum (71 of 102 [69.6%]) samples of patients who had received prior treatment with metronidazole than those who had not received any prior treatment with metronidazole (15 of 37 [40.5%]) and this difference was statistically significant (χ 2 = 8.53, P = 0.003). Metronidazole treatment was initiated from a few days to several weeks before collection of the blood samples in these patients. Two (4.6%) out of 43 sera from control cases were positive for antiamoebic antibody by IHA.
The TechLab E. histolytica II test was positive for E. histolytica Gal/GalNAc lectin antigen in the liver abscess pus of 56 (40.3%) of 139 provisionally diagnosed ALA patients. The TechLab E. histolytica II test detected lectin antigen in 30 (81%) of 37 liver abscess pus of patients which were collected prior to treatment with metronidazole. In contrast, the TechLab E. histolytica test detected the lectin antigen in only 26 (25.5%) of 102 liver pus (χ 2 = 32.61, P < 0.001), collected after initiation of therapy with metronidazole. The probability of E. histolytica antigen detection in liver abscess pus by ELISA was found to be 12 times more in patients who had not received prior treatment with metronidazole (Odds Ratio (OR) = 12.53, 95% Confidence Interval (CI) = 4.55 to 35.86) than in the patients who received prior metronidazole therapy. The OR was statistically significant as the 95% CI of OR was more than 1.
Microscopy of the liver pus demonstrated E. histolytica trophozoites in 10 of 139 (7.2 %) liver abscess specimens, but only 2 (1.4%) pus specimens were positive by culture for E. histolytica. All 10 patients whose liver pus were positive for E. histolytica by microscopy and/or culture were also positive for E. histolytica Gal/GalNAc lectin antigen in the liver pus by the TechLab E. histolytica II test and serum amoebic antibodies by the IHA test.
In the present study, a total of 112 out of 139 (80.6%) provisionally diagnosed ALA patients were diagnosed as ALA and remaining 27 patients were diagnosed as PLA, by following the criteria mentioned in this study elsewhere.
The result of nested multiplex PCR performed on the liver abscess pus is depicted in Figure 1. The nested multiplex PCR test was positive for E. histolytica DNA in 90 (80.4%) of 112 liver abscess pus specimens ( Table 1). The nested multiplex PCR could detect E. histolytica DNA in the liver abscess pus of all 37 ALA patients (100%), who were tested prior to treatment with metronidazole. In contrast, prior metronidazole treatment significantly decreased the ability of the PCR to detect E. histolytica DNA in the liver abscess pus, with only 53 (70.6%) of 75 liver pus samples positive (Fisher's Exact test, P = 0.0006). The probability of E. histolytica DNA detection in liver abscess pus by nested multiplex PCR was 31 times more in patients who had not received prior metronidazole therapy (OR = 31.54, 95% CI = 1.879 to 624.2) than in the patients who received prior metronidazole therapy. The OR was statistically significant as the 95% CI of OR was greater than 1.
The nested multiplex PCR did not detect E. histolytica DNA in a total of 49 liver abscess pus specimens, which included 27 PLA and 22 ALA pus specimens. The probability of negative nested multiplex PCR results, in these 49 liver abscess pus specimens due to PCR inhibitors was ruled out by the inclusion of an internal amplification control (IAC) in the nested PCR reaction.
The comparison of results of nested multiplex PCR and TechLab E. histolytica II ELISA test on liver abscess pus from ALA patients is summarised in the table 1.
The nested multiplex PCR result on urine specimen is shown in Figure 1. The nested multiplex PCR was performed on urine specimen collected from 68 patients (including 53 ALA and 15 PLA) and 43 controls. The nested multiplex PCR test detected E. histolytica DNA in 21 (39.6%) of 53 urine samples collected from patients with ALA ( Table 2). The test did not detect E. histolytica DNA in urine samples collected from all 15 PLA patients and 43 controls.
The nested multiplex PCR test detected E. histolytica DNA in the urine specimens of 4 (17.4%) of 23 ALA patients who were tested prior to treatment with metronidazole and in 17 (56.7%) of 30 ALA patients who were tested after treatment with metronidazole (χ 2 = 6.83, P = 0.009). All of the 4 ALA patients, who did not receive prior treatment with metronidazole and whose urine specimens were positive for E. histolytica DNA, were available for follow-up study. Urine specimens were collected from these patients every week for 4 weeks after starting of the therapy with metronidazole; and were tested for E. histolytica DNA by PCR. It was observed that 2 weeks after treatment with metronidazole, 3 (75%) out of 4 urine specimens became negative for E. histolytica DNA. One urine specimen became negative for E. histolytica DNA after 4 weeks of treatment with metronidazole.

Discussion
In this study, we have made an attempt to detect excretory E. histolytica DNA in urine by applying nested multiplex PCR and to assess the diagnostic potential of the test for detection of E. histolytica DNA in urine for the diagnosis of ALA. Also we have studied the kinetics of the excretion of E. histolytica DNA in urine during the course of therapy with metronidazole.
In our study, 76.8% (86 of 112) of ALA patients were positive for antiamoebic antibody in serum by the IHA. This result was similar to that reported from Bangladesh where serum antiamoebic antibodies were found in 78% of ALA patients [10], but differed from that of the study reported from South Africa, where serum antiamoebic antibodies were found in a higher 99% of ALA patients [35].
Only two out of 10 ALA pus samples which were positive for E. histolytica trophozoite by microscopy were positive for the amoebae by culture and the rest were negative, this may be due to the inhibition of growth by culture itself. In majority of patients, K. pneumoniae was the major bacterial pathogen responsible for PLA and as secondary bacterial infection of ALA. One of 10 ALA pus specimens was positive for Group B Salmonella species, this patient had liver abscess with perihepatic collection, with severe sepsis and disseminated intravascular coagulation, finally the patient died. In this study, the anaerobic culture of liver abscess pus aspirate was not done. Therefore, the possible etiology of liver abscess due to anaerobic organisms such as Bacteroides remained undetermined.
In the present study, 50% (56 of 112) of liver abscess pus were positive for E. histolytica lectin antigen. The sensitivity of the test in our study was observed to be slightly higher than that of the study using the same TechLab E. histolytica II kit (40.7 % sensitiivty) on liver pus reported from Bangladesh [10]. However, results of other studies using polyclonal antibody based ELISA showed a very high sensitivity for the detection of amoebic antigen in the liver pus. Amoebic antigen was detected in liver abscess pus in 97.6% (41/42) of ALA cases by ELISA as reported from China [21] and in 92% and 96% of liver pus by Result of nested multiplex PCR on representative liver abscess pus and urine specimen Figure 1 Result of nested multiplex PCR on representative liver abscess pus and urine specimen. The E. histolytica (EH) and Internal amplification control (IAC) bands are 439 and 305 bp respectively. Lane-1 and 4 are positive for E. histolytica DNA in liver abscess pus and urine specimen respectively; Lane-2, 3 and 5 are negative for E. histolytica DNA; Lane-M, 100 bp DNA ladder (Bangalore genei, Bangalore). using immunoelectrophoresis and ELISA respectively, from India [36].
In developing countries like India where amoebiasis is endemic, antiamoebic drugs and antibiotics are used indiscriminately, making it difficult to obtain an accurate treatment history. Most of the patients in the present study had already been treated with metronidazole at the time of collection of clinical specimens. The serum amoebic antibodies were detected in higher percentage (94.7%) of ALA patients treated earlier with metronidazole, but were detected in only 40.5% of patients who did not receive any prior treatment with metronidazole. This might be due to the late antibody response during the course of the disease.
Unlike serum amoebic antibody detection, E. histolytica lectin antigen was detected in liver pus by TechLab ELISA in a higher percentage (81%) of ALA patients, who were tested prior to treatment with metronidazole, but was detected in only 34.6% of ALA patients, who were tested after the initiation of therapy with metronidazole. This might be due to the rapid clearing of amoebic antigen from the liver pus due to killing of E. histolytica trophozoites on treatment with metronidazole. In the present study E. histolytica DNA was detected in the urine specimen of 4 (17.4%) of 23 ALA patients, who were tested prior to treatment with metronidazole and in 17 (56.7%) of 30 ALA patients, who were tested after treatment with metronidazole by PCR. The probability of E. histolytica DNA detection in urine by PCR was 6 times more in ALA patients who had received prior metronidazole therapy (OR = 6.2, 95% CI = 1.47 to 28.37) than in the ALA patients who did not receive prior metronidazole therapy. The OR was statistically significant as the 95% CI of OR was greater than 1. This might be due to release of increased E. histolytica DNA from the dying E. histolytica trophozoites when metronidazole therapy was initiated, leading to excretion of E. histolytica DNA in the urine. One study has demonstrated that the DNA from dying cells can cross the kidney barrier in rodents and humans and can get excreted with urine, which can be used for genetic analysis [31].
PCR for detection of E. histolytica DNA in liver abscess pus and urine specimen were evaluated for the diagnosis of ALA (McNemar's χ 2 = 26.28, p < 0.0001). The sensitivity of PCR for urine was 39.6%. This was found to be signifi- In the present study, none of the liver abscess pus and urine PCR results were positive for either E. dispar or E. moshkovskii specific PCR products, which confirm the non invasive nature of these species ( Table 2).
The detection of E. histolytica DNA and E. histolytica specific lectin antigen in the serum specimen of ALA patients was not carried out in this study. A controlled prospective study to evaluate the detection of E. histolytica DNA and E. histolytica specific lectin antigen in the serum specimen of ALA patients has been intended to be carried out in future in our laboratory.

Conclusion
The present study for the first time shows that the kidney barrier in ALA patients is permeable to E. histolytica DNA molecule resulting in excretion of E. histolytica DNA in urine which can be detected by PCR. The study also shows that the PCR for detection of E. histolytica DNA in urine of patients with ALA can also be used as a prognostic marker to assess the course of the diseases following therapy by metronidazole. The detection of E. histolytica DNA in urine specimen of ALA patients provides a new approach for the diagnosis of ALA.

Sample details
The subjects in the present study included 139 patients provisionally diagnosed as ALA, who were admitted to JIPMER hospital, Puducherry, as well as 43 controls during a period from September 2004 to March 2006. The provisional diagnosis of ALA was made by the physicians on the basis of patient's history and clinical features, unfortunately these features are often nonspecific to confirm the diagnosis of ALA. Of the 139 provisionally diagnosed ALA patients, 102 had received prior treatment and 37 did not receive prior treatment with metronidazole. The patients and controls were residing in neighboring area of Puducherry. Informed consent was obtained from the patients. This study has been performed with the approval of Institute Research Council of JIPMER, Puducherry.
The control group included 43 individuals who had no history of recent dysentery or diarrhea and whose stool samples were negative for E. histolytica infection by microscopy and culture. Thirty five of the controls were healthy asymptomatic volunteers, and the other 8 patients included, hydatid cyst in liver (n = 2), liver hepatoma (n = 1), liver cirrhosis (n = 3), and viral hepatitis (n = 2).
The diagnosis of ALA was established on the basis of radiological, symptomatological and laboratory criteria as follows [3,10]: (i) a space-occupying lesion in the liver diagnosed by ultra sonography and suggestive of abscess, (ii) clinical symptoms (fever, pain in the right hypochondrium (often referred to the epigastrium), lower chest, back, or tip of the right shoulder), (iii) enlarged and/or tender liver, usually without jaundice, (iv) raised right dome of the diaphragm on chest radiograph, (v) improvement after treatment with antiamoebic drugs (e.g., metronidazole) (vi) positive IHA of serum antibody showing a titer (≥ 1:128) against E. histolytica, (vii) liver aspirate appeared like anchovy sauce but was bacteriologically sterile.

Sample collection
Liver abscess pus: The aspiration of liver abscess pus was indicated only under the following conditions [3]. (i) to rule out a pyogenic abscess; (ii) the failure to respond clinically in 3 to 5 days; (iii) the threat of imminent rupture; and (iv) the prevention of rupture of left-lobe abscess into the pericardium. The liver abscess pus aspirates were performed, only for clinical purposes as judged by the clinicians for the patient care and not for the purpose of this study. Liver abscess pus was obtained under ultrasound guidance from all 139 provisionally diagnosed ALA patients and was stored at -20°C in a sterile container until used.
Urine: Urine specimen could be collected from 68 out of 139 provisionally diagnosed ALA patients and all 43 control group individuals included in the study. 10 ml of urine specimen was collected in a sterile container using aseptic techniques; urine sample was stored at -20°C until use.
Blood: Blood specimen was collected from all 139 provisionally diagnosed ALA patients and 43 control group individuals included in the study. Venous blood (5 ml) was collected in a sterile container; sera were separated and stored at -20°C until used.

Microscopy for Entamoeba
Liver abscess pus: The specimens were examined immediately after the aspiration of abscess. The liver abscess pus was first centrifuged at 2,500 g for 5 mins and a loopful (usually inoculating needle loop) of sediment was mixed with a drop of warm saline on a microscope slide. Microscopic examination of an amoebic abscess aspirate from liver may reveal haematophagous trophozoites.

Culture for Entamoeba
Liver abscess pus: Liver abscess pus specimens were cultured for Entamoeba species in Locke-egg (LE) medium (NIH modification of Boeck and Drbohlav's medium) as previously described [38]. The liver abscess pus was first centrifuged at 2,500 g for 5 mins and a loopful of sediment was inoculated into the LE medium. It is to be noted that in case of culturing Entamoeba from liver abscess aspirates, since the abscess is sterile, bacterial flora (ATCC E. coli) was added before inoculation of amoebae into xenic culture.

Gram stain and bacterial culture for liver abscess pus aspirates
Direct smear Gram staining and bacterial culture was done for all liver abscess pus aspirates. The liver abscess pus specimens were inoculated on to sheep blood agar, MacConkey agar and chocolate agar plates. The MacConkey agar plates were incubated at 37°C for 18-24 hours whereas the blood agar and chocolate agar plates were incubated in a candle jar at 37°C for 48 hours. Based on the colony morphology and result of culture smears, necessary biochemical tests were done to identify bacteria to the species level.

TechLab E. histolytica II ELISA test
The TechLab E. histolytica II test was performed on liver abscess pus specimens to detect E. histolytica as per the method described earlier [10].

Antiamoebic antibody detection by rapid-IHA test
The Rapid-IHA was performed on serum specimen as per the method described earlier [39]. Briefly, double aldehyde stabilized chick red blood cell (RBC) sensitized with the amoebic antigen was used in the test. The haemagglutination test was performed on test serum samples including known positive and negative control sera in each batch. The chick RBC settled quickly and their haemagglutination pattern could be determined within 30 to 45 min of incubation at room temperature with test sera [39]. A titer of ≥ 1:128 was considered positive for ALA [40].

Extraction of Entamoeba genomic DNA
Liver abscess pus: Briefly, 1 ml of liver abscess pus was taken in 1.5 ml centrifuge tube and centrifuged at 12, 000 g for 8 minutes. The supernatant was discarded and 50 μl of pellet was dispersed in 250 μl of lysis buffer (0.25% sodium dodecyl sulfate (SDS) in 0.1 M EDTA, pH 8.0), followed by addition of 100 μg/ml of proteinase K. The lysate was incubated at 55 °C for 2 hours. Then 75 μl of 3.5 M sodium chloride (NaCl) followed by 42 μl of 10% cetyltrimethylammonium bromide (CTAB)/0.7 M NaCl (heated to 55 °C) was added. After the components were mixed, the sample was incubated at 65°C for 30 min. This was followed by extractions with equal volumes of chloroform and then phenol-chloroform-isoamyl alcohol, and the DNA was precipitated with ice cold ethanol. The dried DNA pellet was dissolved in 50 μl of sterile distilled water.
Urine: Briefly, 10 ml of the urine sample was centrifuged at 12,000 g for 15 min at 4 °C. The supernatant was discarded and the pellet was suspended in 500 μl of sterile distilled water. The suspension was boiled for 10 minutes followed by sudden cooling. Next, 5 μl of proteinase-K (10 mg/ml) and 60 μl of 10% SDS were added to the suspension and incubated at 65 °C for three hours. Then 80 μl of 5 M NaCl and 20 μl of 10% CTAB were added to the mixture and incubated at 65 °C for 45 min. This was followed by extractions with equal volumes of chloroform and then phenol-chloroform-isoamyl alcohol. The DNA was precipitated with ice cold ethanol. The dried DNA pellet was dissolved in 50 μl of sterile distilled water.
The protocol for extraction of DNA from liver abscess pus and urine specimen has been modified in our laboratory from CTAB DNA extraction protocol originally described for DNA extraction from amoebic culture [41]. The extracted DNA from liver abscess pus and urine sample was passed through DNA clean-up spin columns (Bangalore Genei KT-62, Bangalore). The DNA was stored at -20°C until used.

Quantification of DNA in liver abscess pus and urine specimen
DNA quantification in spin column purified DNA extract from liver abscess pus and urine specimen was determined by UV absorbance using a Cintra 5 double beam Spectrophotometer. DNA yields were calculated on the basis of UV absorbance × dilution. The purity of the nucleic acid in the samples was estimated by the ratio of readings at 260 nm and 280 nm (OD 260 /OD 280 ).

Primers design
The genus specific primers were designed using nucleotide sequences of  [42]. The primers used in PCR are shown in Table 3.

Standard strains
Three standard strains used in this study were E. histolytica HM-1: IMSS, E. dispar SAW760, and E. moshkovskii Laredo these were used as positive control in the present study. The lyophilized DNA of these strains was generously gifted by Dr. C. Graham Clark from London School of Hygiene & Tropical Medicine, London, UK.
Urine PCR: The PCR mix composition was the same as described earlier for liver abscess pus PCR, except that 1.0 μl of 25 mM MgCl 2 and 2.5 μl of template DNA was added.
The conditions for genus specific PCR were as follows; the PCR mix was subjected to an initial denaturation at 96 °C for 2 minutes, followed by 30 cycles -each consisting of 92 °C for 60 seconds (Denaturation), 56 °C for 60 seconds (Annealing), and 72 °C for 90 seconds (Extension). Finally one cycle of extension at 72 °C for seven minutes was performed. In the species specific nested multiplex PCR (which had multiple primer sets in the same tube), only the annealing temperature was changed to 48 °C, leaving the other parameters of the amplification cycles unchanged.
3.5 μl of the amplification product was separated by electrophoresis through 1.8% agarose gel (Agarose Low EEO, Bangalore genie products, Bangalore, India) containing ethidium bromide in 0.5 × Tris-borate-EDTA at 120 V for 45 min and was visualized under UV light for bands of DNA of appropriate sizes (Figure 1). A negative control