Comparative study on serodiagnostic techniques of Brucella infection in Egypt

dc.AffiliationOctober University for modern sciences and Arts (MSA)
dc.contributor.authorBasyony A.F.
dc.contributor.authorAboulwafa M.M.
dc.contributor.authorHafez M.M.
dc.contributor.authorAbou Gazia K.A.
dc.contributor.otherDepartment of Microbiology and Immunology
dc.contributor.otherFaculty of Pharmacy
dc.contributor.otherModern Sciences and Arts University
dc.contributor.otherEgypt; Microbiology and Immunology Department
dc.contributor.otherFaculty of Pharmacy
dc.contributor.otherAin Shams University
dc.contributor.otherEgypt; Department of Microbiology and Immunology
dc.contributor.otherAnimal Reproduction Research Institute
dc.contributor.otherAgriculture Research Center
dc.contributor.otherEgypt
dc.date.accessioned2020-01-25T19:58:27Z
dc.date.available2020-01-25T19:58:27Z
dc.date.issued2012
dc.descriptionScopus
dc.description.abstractBackground: Brucellosis is a zoonotic disease that affects wild and domestic animals causing a decrease in reproductive efficiency and abortion and can be transmitted to human. The incidence of human disease is closely tied to the prevalence of infection in animals and considered as an important health problem in Egypt. Methods and Findings: In this study, blood specimens from 68 patients that showed clinical signs and/or history of brucellosis and from different investigated animals (76 buffalo, 145 cattle and 191 sheep) were collected and serodiagnosed for Brucella infection. The sera of these blood specimens were first screened by rose bengal plate test (RBPT) and those giving positive reaction were retested by the standard tube agglutination test (SAT), EDTA modified SAT and rivanol test to determine their titers. The results for clinical specimens showed that 89.70%, 82.35%, 66.18% and 58.82% were positive using RBPT, SAT, EDTA modified SAT and rivanol test, respectively. The respective percentages of brucellosis in buffalo were 44.70%, 43.42%, 43.42% and 43.24%; while the respective percentages of brucellosis in cattle were 46.90%, 43.45%, 39.31% and 37.93%. In addition, serological examination of 191 sheep revealed that 60.20%, 56.54%, 53.40% and 51.83% were positive using RBPT, SAT, EDTA modified SAT and rivanol test, respectively. Conclusion: The results give clear evidence for: (i) the real picture of brucellosis surveillance among human cannot be reflected using single serodiagnostic test, (ii) In comparison to human, serodiagnosis of Brucella among animals is less dependent on test type and such dependency took the order sheep > cattle > buffalo, (iii) serodiagnosis of Brucella among buffalo had nearly no dependency on test type. � Under License of Creative Commons Attribution 3.0 License.en_US
dc.description.urihttps://www.scimagojr.com/journalsearch.php?q=21100225606&tip=sid&clean=0
dc.identifier.doihttps://doi.org/10.3823/251
dc.identifier.doiPubMed ID :
dc.identifier.issn19898436
dc.identifier.otherhttps://doi.org/10.3823/251
dc.identifier.otherPubMed ID :
dc.identifier.urihttps://t.ly/ge7J2
dc.language.isoEnglishen_US
dc.relation.ispartofseriesArchives of Clinical Microbiology
dc.relation.ispartofseries3
dc.subjectAnimaliaen_US
dc.subjectBosen_US
dc.subjectBrucellaen_US
dc.subjectOvis ariesen_US
dc.titleComparative study on serodiagnostic techniques of Brucella infection in Egypten_US
dc.typeArticleen_US
dcterms.isReferencedByFreeman, B.A., Vana, L.R., Host-parasite relationships in brucellosis. Infection of normal guinea pig macrophages in tissue culture (1958) Journal of Infectious Diseases, 102 (3), pp. 258-267; Corbel, M.J., Brucellosis: An overview (1997) Emerging Infectious Diseases, 3, pp. 213-221; Rijpens, N.P., Jannes, G., Van Asbroeck, M., Rossau, R., Herman, L.M., Direct detection of Brucella spp. in raw milk by PCR and reverse hybridization with 16S-23S rRNA spacer probes (1996) Applied and Environmental Microbiology, 62 (5), pp. 1683-1688; Pappas, G., Papadimitriou, P., Akritidis, N., Christou, L., Tsianos, E.V., The new global map of human brucellosis (2006) Lancet Infectious Diseases, 6, pp. 91-99; Montasser, M.F., Ibrahim, F.H., Wahab, M.F., Rapid diagnosis of non prolonged febrile illnesses necessitating fever hospital admission (1991) Journal of the Egyptian Public Health Association, 66, pp. 675-692; Afifi, S., Earhart, K., Azab, M.A., Youssef, F.G., El-Sakka, H., Hospital-based surveillance for acute febrile illness in Egypt: A focus on community-acquired bloodstream infections (2005) American Journal of Tropical Medicine and Hygiene, 73, pp. 392-399; Jennings, G., Hajjeh, R., Girgis, F., Fadeel, M., Maksoud, M., Brucellosisas a cause of acute febrile illness in Egypt (2007) Transactions of the Royal Society of Tropical Medicine and Hygiene, 101 (7), pp. 707-713; Doganay, M., Aygen, B., Human brucellosis: An overview (2003) International Journal of Infectious Diseases, 7, pp. 173-182; Wallach, J.C., Miguel, S.E., Baldi, P.C., Guarneru, E., Goldbaum, F.A., Urban outbreak of Brucella melitensis infection in an Argentine family: Clinical and diagnostic aspects (1994) FEMS Immunology and Medical Microbiology, 8, pp. 49-56; Matar, G.M., Khneisser, I.A., Abdel Noor, A.M., Rapid Laboratory confirmation of human brucellosis by PCR analysis of a target sequence on the 31 kliodalton. Brucella antigen DNA (1996) Journal of Clinical Microbiology, 34 (2), pp. 477-478; Araj, G.F., Human brucellosis revisited: A persistant Saga in the Middle East (2000) British Medical Journal (Middle East), 7, pp. 6-15; Solera, J., Lozano, E., Martinez-Alfano, E., Espinosa, A., Castillejos, M.L., Brucellar spondylitis: Review of 35 cases and literature survey (1999) Clinical Infectious Diseases, 29, pp. 1440-1449; Cohen, N., Golik, A., Alon, I., Conservative treatment for Brucella endocarditis (1997) Clinical Cardiology, 20, pp. 291-294; Vallejo, J.G., Stevens, A.M., Dutton, R.V., Kaplan, S.L., Hepatosplenic abscesses due Brucella melitensis: Report of a case involving a child and review of the literature (1996) Clinical Infectious Diseases, 22, pp. 485-489; Colmenero, J.D., Reguera, J.M., Martos, F., Complications associated with Brucella melitensis infection: A study of 530 cases (1996) Medicine (Baltimore), 75, pp. 195-211; Franco, M.P., Mulder, M., Gilman, R.H., Smits, H.L., Human brucellosis (2007) Lancet Infectious Diseases, 7, pp. 775-786; Odeh, M., Pick, N., Oliven, A., Deep vein thrombosis associated with acute brucellosis: Case report (2000) Angiology, 51, pp. 253-256; Mousa, A.R., Koshy, T.S., Araj, G.F., Marafie, A.A., Muhtaseb, S.A., Brucella meningitis: Presentation, diagnosis and treatment; a prospective study of ten cases (1986) Quarterly Journal of Nuclear Medicine, 60, pp. 873-885; Odeh, M., Oliven, A., Acute brucellosis associated with massive proteinuria (1996) Nephron, 72, pp. 688-689; Abd Elrazak, M., Brucella optic neuritis (1991) Archives of Internal Medicine, 151, pp. 776-778; Corbel, M.J., (2006) Brucellosis In Humans and Animals, , World Health Organization, Food and Agriculture Organization of the United Nations, International Office of Epizootics, World Health Organization. Geneva, Switzerland. ISBN: 9241547138, 9789241547130; Refai, M., Incidence and control of brucellosis in the Near East region (2002) Veterinary Microbiology, 90, pp. 81-110; Alton, G.G., Jones, L.M., Angus, R.D., Verger, J.M., (1988) Techniques For the Brucellosis Laboratory, , Institut National de la Recherche Agronomique (INRA), Paris, France, ISBN: 278000428; Macmillan, A.P., Cockrem, D.S., Reduction of non-specific reaction to the Brucella abortus serum agglutination test by addition of EDTA (1985) Research In Veterinary Science, 38 (3), pp. 288-291; Fouad, K., Nour El-Din, A., Salah, A., Murad, A., Study of Brucella infection as an occupational risk among abattoir workers in Alexandria (1996) Bulletin of Alexandria Faculty of Medicine, 32, pp. 299-306; Alsubaie, S., Almuneef, M., Alshaalan, M., Balkhy, H., Albanyan, E., Acute brucellosis in Saudi families: Relationship between Brucella serology and clinical symptoms (2005) International Journal of Infectious Diseases, 9, pp. 218-224; Nimri, L.F., Diagnosis of recent and relapsed cases of human brucellosis by PCR assay (2003) BMC Infectious Diseases, 3, p. 5; Kazemi, B., Namin, Y.A.S., Dowlatshahi, M., Bandepour, B., Kafilzadeh, F., Detection of Brucella by peripheral blood PCR and comparison with culture and serological methods in suspected cases (2008) Iranian Journal of Public Health, 37 (4), pp. 96-102; Chauhan, H.C., Chandel, B.S., Shah, N.M., Seroprevalence of brucellosis in buffaloes in Gujrat (2000) Indian Veterinary Journal, 77, pp. 1105-1106; Nasir, A.A., Parrveen, Z., Shah, M.A., Rashid, M., Prevalence of brucellosis in animals at government and private farms in Punjab (2004) Pakistan Veterinary Journal, 24, pp. 144-146; Genc, O., Otlu, S., Sahin, M., Aydin, F., Gokce, H.I., Seroprevalence of brucellosis and leptospirosis in aborted dairy cows (2005) Turkish Journal of Veterinary and Animal Sciences, 29, pp. 359-366; Otlu, S., Sahin, M., Atabay, H.I., Unver, A., Serological investigations of brucellosis in cattle, farmers and veterinarians in the Kars District of Turkey (2008) Acta Veterinaria Brno, 77, pp. 117-121; Sahin, M., Genc, O., Unver, A., Otlu, S., Investigation of bovine brucellosis in the Northeastern Turkey (2008) Tropical Animal Health and Production, 40, pp. 281-286; Al-Talafhah, A.H., Lap, S.Q., Al-Tarazi, Y., Epidemiology of ovine brucellosis in Awassi sheep in Northern Jordan (2003) Preventive Veterinary Medicine, 60, pp. 297-306; Gupta, V.K., Deepak, K.V., Rout, P.K., Singh, S.V., Vihan, V.S., Polymerase chain reaction (PCR) for detection of Brucella melitensis in goat milk (2006) Small Ruminant Research, 65, pp. 79-84; Nashwa, M.H., Hoda, M.Z., Sami, S.A., Identification and differentiation of Brucella melitensis Rev.1 vaccines and B. melitensis biovar 3 field isolates in Egypt by serological and PCR-RFLP techniques (2007) Journal of Applied Sciences Research, 3, pp. 841-847; Otlu, S., Sahin, M., Unver, A., Celebi, O., Detection of Brucella melitensis and Chlamydophila abortus antibodies in aborting sheep in the Kars province of Turkey (2007) The Bulletin of the Veterinary Institute In Pulawy, 51, pp. 493-495; Celebi, O., Atabay, H.I., Seroepidemiological investigation of brucellosis in sheep abortions in Kars, Turkey (2009) Tropical Animal Health and Production, 41, pp. 115-119; Sirmatel, F., Turker, M., Bozkurt, A.I., Evaluation of the methods used for the serologic diagnosis of brucellosis (2002) Mikrobiyoloji Bulteni, 36, pp. 161-167; Gall, D., Nielsen, K., Serological diagnosis of bovine brucellosis: A review of test performance and cost comparison (2004) Scientific and Technical Review of the Office International Des Epizooties, 23, pp. 989-1002; Ertek, M., Yazgi, H., Ozkurt, Z., Ayyildiz, A., Parlak, M., Comparison of the diagnostic value of the standard tube agglutination test and the ELISA IgG and IgM in patients with brucellosis (2006) Turkish Journal of Medical Sciences, 36 (3), pp. 159-163; Trap, D., Garin, B., Moutou, F., Gaumont, R., Bovine brucellosis: Elimination of non-specific sero-agglutination by using EDTA and agglutination at 56C (1985) Revue De MedecineVeterinaire, 136 (5), pp. 399-409; Otto, M., Radostits, C., Gay, C., Douglas, C., Blood, K., (2000) Veterinary Medicine, , 9th Ed. W.B. Saunders Co. London, UK. ISBN: 0702026042; Mikolon, A.B., Gardner, I.A., Hietala, S.K., Hernandez-de-Anda, J., Chamizo-Pestana, E., Evaluation of North American antibody detection tests for diagnosis of brucellosis in goats (1998) Journal of Clinical Microbiology, 36 (6), pp. 1716-1722
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