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. 2006 Jul;98(3):286-96.
doi: 10.1016/j.actatropica.2006.06.003. Epub 2006 Jul 12.

Long-term reduction of Trypanosoma cruzi infection in sylvatic mammals following deforestation and sustained vector surveillance in northwestern Argentina

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Long-term reduction of Trypanosoma cruzi infection in sylvatic mammals following deforestation and sustained vector surveillance in northwestern Argentina

L A Ceballos et al. Acta Trop. 2006 Jul.

Abstract

Long-term variations in the dynamics and intensity of sylvatic transmission of Trypanosoma cruzi were investigated around eight rural villages in the semiarid Argentine Chaco in 2002-2004 and compared to data collected locally in 1984-1991. Of 501 wild mammals from 13 identified species examined by xenodiagnosis, only 3 (7.9%) of 38 Didelphis albiventris opossums and 1 (1.1%) of 91 Conepatus chinga skunks were infected by T. cruzi. The period prevalence in opossums was four-fold lower in 2002-2004 than in 1984-1991 (32-36%). The infection prevalence of skunks also decreased five-fold from 4.1-5.6% in 1984-1991 to 1.1% in 2002-2004. Infection in opossums increased with age and from summer to spring in both study periods. The force of infection per 100 opossum-months after weaning declined more than six-fold from 8.2 in 1988-1991 to 1.2 in 2002-2004. Opossums were mainly infected by T. cruzi lineage I and secondarily by lineage IId in 1984-1991, and only by T. cruzi I in 2002-2004; skunks were infected by T. cruzi IId in 1984-1991 and by IIc in 2002-2004. The striking decline of T. cruzi infection in opossums and skunks occurred in parallel to community-wide insecticide spraying followed by selective sprays leading to very low densities of infected Triatoma infestans in domestic and peridomestic habitats since 1992; to massive deforestation around one of the villages or selective extraction of older trees, and apparent reductions in opossum abundance jointly with increases in foxes and skunks. These factors may underlie the dramatic decrease of T. cruzi infection in wild reservoir hosts.

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Figures

Fig. 1
Fig. 1
Map showing capture sites of wild mammals in the Amamá area, 2002–2004.
Fig. 2
Fig. 2
Capture of sylvatic mammals per unit effort according to type of trap (Sherman, National) in communities with different landscape. March 2003, July 2003, November 2003 and July 2004. Other communities: La Curva, San Luis, Lote S, Pampa Pozo. Numbers on top of bars represent the total number of trap-days per community.
Fig. 3
Fig. 3
Comparison of prevalence of Trypanosoma cruzi infection as determined by xenodiagnosis in opossums by age class (A) and seasons (B) in 1988–1991 (taken from Schweigmann et al., 1999) and 2002–2004 in the Amamá area.
Fig. 4
Fig. 4
Amplification of the intergenic region of the mini-exon genes (A), the D7 DNA ribosomal 24S-alfa domain (B) and A10 genomic marker (C); lanes (1) negative control; 2–5 Didelphis albiventris T. cruzi I (2) and (3) are the same individual on different capture occasions; (6) Conepatus chinga skunk T. cruzi IIc; (7) reference strain of lineage IIb (A and B) and lineage IIa (C); (8) reference strain of lineage I; (9), 100 bp ladder.

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