Detection of cross infections by Leishmania spp. and Trypanosoma spp. in dogs using indirect immunoenzyme assay, indirect fluorescent antibody test and polymerase chain reaction

被引:13
作者
Viol, M. A. [1 ]
Lima, V. M. F. [1 ]
Aquino, M. C. C. [1 ]
Gallo, G. [1 ]
Alves, I. P. [1 ]
Generoso, D. [2 ]
Perri, S. H. V. [1 ]
Lucheis, S. B. [2 ]
Langoni, H. [2 ]
Nunes, C. M. [1 ]
Bresciani, K. D. S. [1 ]
机构
[1] UNESP Univ Estadual Paulista, Fac Odontol, BR-16050680 Sao Paulo, Brazil
[2] Univ Estadual Paulista, Fac Med Vet & Zootecnia, Sao Paulo, Brazil
关键词
CANINE VISCERAL LEISHMANIASIS; CHRONIC CHAGAS-DISEASE; RIO-DE-JANEIRO; SEROLOGICAL SURVEY; URBAN AREAS; FOLLOW-UP; DIAGNOSIS; CRUZI; PCR; AMPLIFICATION;
D O I
10.1007/s00436-012-2999-2
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
The aim of this study was to detect cross infections by Leishmania spp. and Trypanosoma spp. using enzyme-linked immunosorbent assay (ELISA), indirect fluorescent antibody test (IFAT) and polymerase chain reaction (PCR). Thus, 408 blood samples were collected from dogs domiciled in Ara double dagger atuba Municipality, So Paulo State, Brazil; the dogs were of both sexes, of several breeds and aged 6 months. For Leishmania spp., 14.95 % (61 out of 408) of dogs were reactive using IFAT. Positivity was 20.10 % (82 out of 408) using ELISA and 29.66 % (121 out of 408) using PCR, with significant differences for the sex and age of these animals (p < 0.05). For Trypanosoma spp., antibody occurrence using ELISA was 10.54 % (43 out of 408), while PCR indicated 2.45 % (10 out of 408) positive dogs. Using IFAT, 10.29 % (42 out of 408) of animals were considered positive and only sex showed a significant difference (p < 0.05). In this study, 10.54 % (43 out of 408) of animals were seropositive according to ELISA for Trypanosoma spp., of which 79.07 % (34 out of 43) showed positive results in the molecular diagnosis for Leishmania spp., while of the 10.29 % (42 out of 408) positive dogs according to IFAT, 95.24 % (40 out of 42) had confirmed infection by this parasite. The obtained results demonstrate evidence of cross infections by both protozoa in the animals analysed in this study.
引用
收藏
页码:1607 / 1613
页数:7
相关论文
共 50 条
  • [31] An indirect ELISA for detection of Theileria spp. antibodies using a recombinant protein (rTlSP) from Theileria luwenshuni
    He, Haining
    Li, Youquan
    Liu, Junlong
    Liu, Zhijie
    Yang, Jifei
    Liu, Aihong
    Chen, Ze
    Ren, Qiaoyun
    Guan, Guiquan
    Liu, Guangyuan
    Luo, Jianxun
    Yin, Hong
    EXPERIMENTAL PARASITOLOGY, 2016, 166 : 89 - 93
  • [32] Semi-Quantitative, Duplexed qPCR Assay for the Detection of Leishmania spp. Using Bisulphite Conversion Technology
    Gow, Ineka
    Millar, Douglas
    Ellis, John
    Melki, John
    Stark, Damien
    TROPICAL MEDICINE AND INFECTIOUS DISEASE, 2019, 4 (04)
  • [33] The cooling on the diagnostic of Salmonella spp. using traditional microbiologic method and the polymerase chain reaction in poultry carcasses
    Possebon, Fabio Sossai
    Zuccolo Paschoal da Costa, Luis Felipe
    Yamatogi, Ricardo Seiti
    Rodrigues, Marianna Vaz
    Sudano, Mateus Jose
    de Almeida Nogueira Pinto, Jose Paes
    CIENCIA RURAL, 2012, 42 (01): : 131 - 135
  • [34] An enhanced method for the identification of Leishmania spp. using real-time polymerase chain reaction and sequence analysis of the 7SL RNA gene region
    Stevenson, Lindsay G.
    Fedorko, Daniel P.
    Zelazny, Adrian M.
    DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2010, 66 (04) : 432 - 435
  • [35] Natural Infection of Nyssomyia neivai by Leishmania (Viannia) spp. in the State of Parana, Southern Brazil, Detected by Multiplex Polymerase Chain Reaction
    Oliveira, Diego Molina
    Reinhold-Castro, Karin Rosi
    Zandonadi Bernal, Marcos Vinicius
    de Oliveira Legriffon, Cristiane Machado
    Campana Lonardoni, Maria Valdrinez
    Teodoro, Ueslei
    Verzignassi Silveira, Thais Gomes
    VECTOR-BORNE AND ZOONOTIC DISEASES, 2011, 11 (02) : 137 - 143
  • [36] Development of a multiplex polymerase chain reaction assay for diarrheagenic Escherichia coli and Shigella spp. and its evaluation on colonies, culture broths, and stool
    Taniuchi, Mami
    Walters, Carol C.
    Gratz, Jean
    Maro, Athanasia
    Kumburu, Happiness
    Serichantalergs, Oralak
    Sethabutr, Orntipa
    Bodhidatta, Ladaporn
    Kibiki, Gibson
    Toney, Denise M.
    Berkeley, Lynette
    Nataro, James P.
    Houpt, Eric R.
    DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2012, 73 (02) : 121 - 128
  • [37] Detection and differentiation of Leptospira spp. serovars in bovine semen by polymerase chain reaction and restriction fragment length polymorphism
    Heinemann, MB
    Garcia, JF
    Nunes, CM
    Gregori, F
    Higa, ZMM
    Vasconcellos, SA
    Richtzenhain, LJ
    VETERINARY MICROBIOLOGY, 2000, 73 (04) : 261 - 267
  • [38] DETECTION OF Theileria AND Anaplasma spp. IN CARRIER BUFFALOES (Bubalus bubalis) BY POLYMERASE CHAIN REACTION IN TAMIL NADU, INDIA
    Ponnudurai, Gurusamy
    Rani, Natarajan
    Rubinibala, Balan
    Alagesan, Alagarsamy
    Saravanan, Ramasamy
    BUFFALO BULLETIN, 2022, 41 (04): : 571 - 577
  • [39] Comparison of polymerase chain reaction (PCR) and conventional cultivation methods for detection of carriers of Salmonella spp. in cattle and buffalo
    Ahmadi M.
    Dalirnaghadeh B.
    Aski H.S.
    Khoshbakht R.
    Comparative Clinical Pathology, 2010, 19 (3) : 251 - 255
  • [40] Detection of pathogenic Leptospira spp. through TaqMan polymerase chain reaction targeting the LipL32 gene
    Stoddard, Robyn A.
    Gee, Jay E.
    Wilkins, Patricia P.
    McCaustland, Karen
    Hoffmaster, Alex R.
    DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2009, 64 (03) : 247 - 255