Infectivity for mice of Trypanosoma cruzi I and II strains isolated from different hosts

被引:23
作者
Bértoli, M [1 ]
Andó, M [1 ]
Toledo, MJD [1 ]
De Araújo, SM [1 ]
Gomes, ML [1 ]
机构
[1] Univ Estadual Maringa, Lab Doenca Chagas, Dept Anal Clin, BR-87020900 Maringa, Parana, Brazil
关键词
D O I
10.1007/s00436-005-0122-7
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
In this paper, the infectivity for mice of Trypanosoma cruzi I and II strains isolated from sylvatic animals, triatomines, and humans is determined using fresh blood examination, hemoculture, culture of macerated organs, and polymerase chain reaction (PCR). Six strains were considered to have low infectivity (9.1-18.2%), five medium (27.3-45.4%), and one high (100.0%). Infectivity of T. cruzi strains isolated from sylvatic animals was significantly higher than that of strains isolated from humans and triatomines (p=0.0141). No significant difference was observed between the infectivity of T. cruzi I and II strains. The parasite was detected by fresh blood examination in one strain, by hemoculture and culture of macerated organs in four strains, and by PCR in all strains. We conclude that the infectivity is related to the host from which the strains were isolated, but the infectivity is not related to the genetic group of the parasite. We also conclude that the majority of the strains studied have low and medium infectivity for mice, and that PCR is an important tool to detect T. cruzi in strains with this biological characteristic.
引用
收藏
页码:7 / 13
页数:7
相关论文
共 51 条
[31]  
MANGIA RH, 2001, C 28 ANN M BAS RES C, P164
[32]   Trypanosoma cruzi recombinant complement regulatory protein:: a novel antigen for use in an enzyme-linked immunosorbent assay for diagnosis of Chagas' disease [J].
Meira, WSF ;
Galvo, LMC ;
Gontijo, ED ;
Machado-Coelho, GLL ;
Norris, KA ;
Chiari, E .
JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (10) :3735-3740
[33]   Trypanosoma cruzi:: Sensitivity of the polymerase chain reaction for detecting the parasite in the blood of mice infected with different clonal genotypes [J].
Miyamoto, CT ;
Gomes, ML ;
Marangon, A ;
Araújo, M ;
Bahia, MT ;
Lana, M ;
Toledo, M .
EXPERIMENTAL PARASITOLOGY, 2006, 112 (03) :198-201
[34]   Progress towards interruption of transmission of Chagas disease [J].
Moncayo, A .
MEMORIAS DO INSTITUTO OSWALDO CRUZ, 1999, 94 :401-404
[35]   An alternative approach to evaluating the intraspecific genetic variability of parasites [J].
Oliveira, RP ;
Macedo, AM ;
Chiari, E ;
Pena, SDJ .
PARASITOLOGY TODAY, 1997, 13 (05) :196-200
[36]   Trypanosoma cruzi in the sylvatic environment:: distinct transmission cycles involving two sympatric marsupials [J].
Pinho, AP ;
Cupolillo, E ;
Mangia, RH ;
Fernandes, O ;
Jansen, AM .
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 2000, 94 (05) :509-514
[37]   Trypanosoma cruzi:: Impact of clonal evolution of the parasite on its biological and medical properties [J].
Revollo, S ;
Oury, B ;
Laurent, JP ;
Barnabé, C ;
Quesney, V ;
Carrière, V ;
Noël, S ;
Tibayrenc, M .
EXPERIMENTAL PARASITOLOGY, 1998, 89 (01) :30-39
[38]   Differential expression of a virulence factor, the trans-sialidase, by the main Trypanosoma cruzi phylogenetic lineages [J].
Risso, MG ;
Garbarino, GB ;
Mocetti, E ;
Campetella, O ;
Cappa, SMG ;
Buscaglia, CA ;
Leguizamón, MS .
JOURNAL OF INFECTIOUS DISEASES, 2004, 189 (12) :2250-2259
[39]  
SCHLEMPER B R JR, 1986, Memorias do Instituto Oswaldo Cruz, V81, P191
[40]  
Silveira A. C., 1994, Revista da Sociedade Brasileira de Medicina Tropical, V27, P11, DOI 10.1590/S0037-86821994000100003