Detection and genotyping of cryptosporidium spp. in diarrheic stools by PCR/RFLP analyses

To compare microscopy and polymerase chain reaction (PCR) as methods for diagnosing Cryptosporidium spp. and identifying the genotype of the parasite in diarrheic stool. Materials and methods: Stool samples from diarrheic patients admitted to Dokuz Eylül University Medical Faculty were collected on a specific day of the week. Stool samples sent to our laboratory from patients affected by a diarrhea epidemic in İzmir were also included in the study. A total of 162 stool samples were examined by microscopic and molecular methods, and the validity of the molecular method was investigated. Results: Using Kinyoun acid-fast dye, Cryptosporidium spp. was found in 18 stool samples. Using PCR, Cryptosporidium spp.-specific bands were found in 15 of these cases. In stool samples that showed no Cryptosporidium spp. by Kinyoun acid-fast dye, a parasite-specific band was obtained in 6 of 144 cases. The restriction fragment length polymorphism (RFLP) method was applied in the cases in which the parasite was found with PCR. Cryptosporidium meleagridis was found in the stool sample of 1 case, and Cryptosporidium parvum-specific bands were seen in the stool samples of 20 cases. The mean age of those who were diagnosed with Cryptosporidium spp. was significantly lower than the mean age of study participants who were not diagnosed with the parasite (P = 0.006). It was found that the families of 44.4% of those diagnosed with Cryptosporidium spp. had similar complaints. This rate was statistically significant (P = 0.01). It was found that 88.9% of those diagnosed with Cryptosporidium spp. drank artesian and well water, and 11.1% drank bottled water. The rate of Cryptosporidium spp. in those who drank artesian and well water was significantly higher than the rate of those who drank city or bottled water (P < 0.001). While the Kinyoun acid-fast method is considered the gold standard, the sensitivity of the PCR method is 83.3% and the selectivity is 95.8%. Conclusion: It can be concluded that Kinyoun acid-fast dye, which can be used as a referential diagnostic method, has some limitations and that PCR is more sensitive and allows for identification of the parasite genotype.

Detection and genotyping of cryptosporidium spp. in diarrheic stools by PCR/RFLP analyses

To compare microscopy and polymerase chain reaction (PCR) as methods for diagnosing Cryptosporidium spp. and identifying the genotype of the parasite in diarrheic stool. Materials and methods: Stool samples from diarrheic patients admitted to Dokuz Eylül University Medical Faculty were collected on a specific day of the week. Stool samples sent to our laboratory from patients affected by a diarrhea epidemic in İzmir were also included in the study. A total of 162 stool samples were examined by microscopic and molecular methods, and the validity of the molecular method was investigated. Results: Using Kinyoun acid-fast dye, Cryptosporidium spp. was found in 18 stool samples. Using PCR, Cryptosporidium spp.-specific bands were found in 15 of these cases. In stool samples that showed no Cryptosporidium spp. by Kinyoun acid-fast dye, a parasite-specific band was obtained in 6 of 144 cases. The restriction fragment length polymorphism (RFLP) method was applied in the cases in which the parasite was found with PCR. Cryptosporidium meleagridis was found in the stool sample of 1 case, and Cryptosporidium parvum-specific bands were seen in the stool samples of 20 cases. The mean age of those who were diagnosed with Cryptosporidium spp. was significantly lower than the mean age of study participants who were not diagnosed with the parasite (P = 0.006). It was found that the families of 44.4% of those diagnosed with Cryptosporidium spp. had similar complaints. This rate was statistically significant (P = 0.01). It was found that 88.9% of those diagnosed with Cryptosporidium spp. drank artesian and well water, and 11.1% drank bottled water. The rate of Cryptosporidium spp. in those who drank artesian and well water was significantly higher than the rate of those who drank city or bottled water (P < 0.001). While the Kinyoun acid-fast method is considered the gold standard, the sensitivity of the PCR method is 83.3% and the selectivity is 95.8%. Conclusion: It can be concluded that Kinyoun acid-fast dye, which can be used as a referential diagnostic method, has some limitations and that PCR is more sensitive and allows for identification of the parasite genotype.

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  • Xiao Cryptosporidium taxonomy: recent advances and L. implications for public health. Clin Microbiol Rev 2004; 17: 72-97. 2.
  • Guyot K, Follet-Dumoulin A, Recourt C, Lelièvre E, Cailliez
  • JC, Dei Cas E. PCR-restriction fragment length polymorphism
  • analysis of a diagnostic 452-base-pair DNA fragment
  • discriminates between Cryptosporidium parvum and C.
  • meleagridis and between C. parvum isolates of human and
  • animal origin. Appl Environ Microbiol 2002; 68: 2071-76.
  • Morgan UM, Pallant L, Dwyer BW, Forbes DA, Rich G, Th ompson RCA. Comparison of PCR and microscopy for detection of Cryptosporidium parvum in human fecal specimens: clinical trial. J Clin Microbiol 1998; 36: 995-98.
  • Kaushik K, S Khurana, Wanchu A, Malla N. Evaluation of staining techniques, antigen detection and nested PCR for the diagnosis of cryptosporidiosis in HIV seropositive and seronegative patients. Acta Trop 2008; 107: 1-7.
  • Ramirez NE, Ward LA, Sreevatsan S. A review of the biology and epidemiology of cryptosporidiosis in humans and animals. Microbes Infect 2004; 6: 773-85.
  • Guk SM, Yong TS, Park SJ, Park JH, Chai JY. Genotype and animal infectivity of a human isolate of Cryptosporidium parvum in the Republic of Korea. Korean J Parasitol 2004; 42: 85-9.
  • McLauchlin J, Amar C, Pedraza-Diaz S, Nichols GL. Molecular epidemiological analysis of Cryptosporidium spp. in the United Kingdom: results of genotyping Cryptosporidium spp. in 1705 fecal samples from humans and 105 fecal samples from livestock animals. Journal of Clinical Microbiology 2000; 38: 3984-90.
  • Yılmaz Ş, Dursun M, Ertem M, Canoruc F, Turhanoğlu A. Th e epidemiological aspects of irritable bowel syndrome in Southeastern Anatolia: a stratifi ed randomised community- based study. Int J Clin Pract 2005; 59: 361-69.
  • Garcia LS, Brewer TC, Bruckner DA, Shimizu RY. Acid-fast staining Cryptosporidium from human fecal specimens. Clin Microbiol Newslett 1983; 5: 60-2.
  • McLauchlin J, Pedraza-Diaz S, Amar-Hoetzeneder C, Nichols GL. Genetic characterization of Cryptosporidium strains from 218 patients with diarrhea diagnosed as having sporadic cryptosporidiosis. J Clin Microbiol 1999; 37: 3153-58.
  • Public Health Laboratory Service Study Group.
  • Cryptosporidiosis in England and Wales; prevalence and clinical and epidemiological features. Br Med J 1990; 300: 774- 77.
  • Guyot K, Follet-Dumoulin A, Lelievre E, Sarfati C, Rabodonirina M, Nevez G et al. Molecular characterization of Cryptosporidium isolates obtained from humans in France. J Clin Microbiol 2001; 39: 3472-80.
  • Abe N, Kimata I, Iseki M. Identifi cation of genotypes of Cryptosporidium parvum isolates from a patient and a dog in Japan. J Vet Med Sci 2002; 64: 165-68.
  • Pereira MGC, Atwill ER, Barbosa AP, Silva SAE, García-Zapata MTA. Intra-familial and extra-familial risk factors associated with Cryptosporidium parvum infection among children hospitalized for diarrhea in Goiania, Goias, Brazil. Am J Trop Med Hyg 2002; 66: 787-93.
  • Hunter PR, Hughes S, Woodhouse S, Syed Q, Verlander NQ, Chalmers RM et al. Sporadic cryptosporidiosis case-control study with genotyping. Emerg Infect Dis 2004; 10: 1241-49.
  • Khan WA, Rogers KA, Karim MM, Ahmed S, Hibberd PL, Calderwood SB et al. Cryptosporidiosis among Bangladeshi children with diarrhea: a prospective, matched, case-control study of clinical features, epidemiology and systemic antibody responses. Am J Trop Med Hyg 2004; 71: 412-19.
  • Balatbat AB, Jordan GW, Tang YJ, Silva J. Detection of Cryptosporidium parvum DNA in human feces by nested PCR. J Clin Microbiol 1996; 34: 1769-72.
  • Lindergard G, Nydam DV, Wade SE, Schaaf SL, Mohammed HO. A novel multiplex polymerase chain reaction approach for detection of four human infective Cryptosporidium isolates: Cryptosporidium parvum, types H and C, Cryptosporidium canis, and Cryptosporidium felis in fecal and soil samples. J Vet Diagn Invest 2003; 15: 262-67.
  • Amar CFL, Dear PH, McLauchlin J. Detection and identifi cation by real time PCR/RFLP analyses of Cryptosporidium species from human faeces. Let Appl Microbiol 2004; 38: 217-22.
  • Morgan UM, Pallant L, Dwyer BW, Forbes DA, Rich G, Th ompson RCA. Comparison of PCR and microscopy for detection of Cryptosporidium parvum in human fecal specimens: clinical trial. J Clin Microbiol 1998; 36: 995-98.
  • İnceboz T, Sarı B, Orhan V. Gastrointestinal şikayetleri olan olgularda Cryptosporidium araştırılması. T Parazitol Derg 2002; 26: 149-50.
  • Atambay M, Daldal N, Çelik T. Malatya’da ishalli dışkılarda Cryptosporidium spp. araştırılması. T Parazitol Derg 2003; 27: 12-4.
  • Doğancı T, Araz E, Ensari A, Tanyüksel M, Doğancı L. Detection of Cryptosporidium parvum infection in childhood using various techniques. Med Sci Monitor 2002; 8: 223-26.
  • Soba B, Petrovec M, Mioc V, Logar J. Molecular characterisation of Cryptosporidium isolates from humans in Slovenia. Clin Microbiol Infect 2006; 12: 918-21.
  • Gatei W, Wamae CN, Mbae C, Waruru A, Mulinge E, Waithera T et al. Cryptosporidiosis: prevalence, genotype analysis, and symptoms associated with infections in children in Kenya. Am J Trop Med Hyg 2006; 75: 78-82.
Turkish Journal of Medical Sciences-Cover
  • ISSN: 1300-0144
  • Yayın Aralığı: Yılda 6 Sayı
  • Yayıncı: TÜBİTAK
Sayıdaki Diğer Makaleler

Assessment of the left atrial longitudinal myocardial function by the strain and strain rate echocardiography in patients with rheumatic mitral stenosi

Hanefi Yekta GÜRLERTOP, Muhammed Hakan TAŞ, Enbiya AKSAKAL, Şule KARAKELLEOĞLU, Mustafa Kemal EROL, Mehmet Ali ELBEY, Serdar SEVİMLİ, Fuat GÜNDOĞDU

A practical calculation method for predetermination of amount and duration of expander application

Önder TAN

Hydatid cyst viability: the effect of scolicidal agents on the scolex in the daughter cyst

Nurdan ÇAY, Mustafa KARAOĞLANOĞLU, Melike Ruşen METİN, Ömer Faruk AKINCI, Hüseyin ÇETİN, Mustafa ULUKANLIGİL

Assessment of the left atrial longitudinal myocardial function by Assessment of the left atrial longitudinal myocardial function by the strain and strain rate echocardiography in patients with rheumatic mitral stenosis*

Enbiya AKSAKAL, Serdar SEVİMLİ, Hanefi Yekta GÜRLERTOP, Mehmet Ali ELBEY, Muhammed Hakan TAŞ, Fuat GÜNDOĞDU, Mustafa Kemal EROL, Şule KARAKELLEOĞLU

An investigation of changes in ocular blood fl ow in rabbits with long-term hyperhomocysteinemia using color doppler ultrasonography

Nazmi NARİN, Abdulhakim COŞKUN, Abdulkerim COŞKUN, Figen NARİN, Sertaç Hanedan ONAN, Ruşen EREZ, Ali BAYKAN, Muammer Hakan POYRAZOĞLU

Physicians’ attitudes toward clinical ethics consultation: a research study from Turkey

Funda Gülay KADIOĞLU, Rana CAN, Nuri Selim KADIOĞLU, ÖNER Sibel YALÇIN, Selda OKUYAZ

Left main coronary calcifi cation mimicking dissection: multislice computed tomography saves the patient from emergent surgery

Hüseyin AYHAN, Nihal Akar BAYRAM, RUŞEN Melike METİN, Telat KELEŞ, Tahir DURMAZ, Engin BOZKURT

Documentation of small intestine atresias: a single-institution experience in Turkey (22 cases)

Demet ETİT, Süheyla CUMURCU, Fatma Nur AKTAŞ, Deniz ALTINEL, Rafet BEYHAN, Naciye Ümit BAYOL

ICSI outcome in severely oligoasthenozoospermic patients and its relationship to prewash progressive sperm motility

Aylin AYRIM, Nilgün TURHAN, Aslıhan PEKEL, Ömer BAYRAK

Histological changes in the healing process of sclerotomy sites aft er 20-gauge and transconjunctival 23- and 25-gauge incisions in experimental model

BARUT Özlem SELVER, Nilüfer KOÇAK, Banu LEBE, Süleyman KAYNAK, Mehmet Özgür ZENGİN