Claudia I. Muñoz-García

Dr. Claudia I. Muñoz-García


Research Focus & Metrics

Academic Career Length

16Years (2011-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 September 2011 in Veterinary Parasitology
Verified
Journal Article
Closed access
LCL. Chitimia
L. Chitimia
CMClaudia I. Muñoz-García
Claudia I. Muñoz-García
DSD. Sánchez-Velasco
D. Sánchez-Velasco
VLV. Lizana
V. Lizana
LALaura del Rio Alonso
Laura del Rio Alonso
EBE. Berriatua
E. Berriatua

1 March 2014 in Preventive Veterinary Medicine
Verified
Journal Article
Closed access
LALaura del Rio Alonso
Laura del Rio Alonso
LCL. Chitimia
L. Chitimia
ACA. Cubas
A. Cubas
IVI. Victoriano
I. Victoriano
PRPilar De la Rua
Pilar De la Rua
EBEduardo Berriatua
Eduardo Berriatua

1 August 2019 in Ticks and Tick-borne Diseases
Verified
Journal Article
Closed access
SSSokani Sanchez-Montes
Sokani Sanchez-Montes
AIAna Belem Isaak-Delgado
Ana Belem Isaak-Delgado
CGCarmen Guzmán-Cornejo
Carmen Guzmán-Cornejo
EREmilio Rendón-Franco
Emilio Rendón-Franco
CMClaudia I. Muñoz-García
Claudia I. Muñoz-García
IBIngeborg Becker
Ingeborg Becker

7 February 2022 in Infection, Genetics and Evolution
Verified
Journal Article
Open access
FMFernando Martínez-Hernández
Fernando Martínez-Hernández
BOBrizia Oria-Martínez
Brizia Oria-Martínez
EREmilio Rendón-Franco
Emilio Rendón-Franco
GVGuiehdani Villalobos
Guiehdani Villalobos
CMClaudia I. Muñoz-García
Claudia I. Muñoz-García
Trypanosoma cruzi is a protozoan parasite responsible for Chagas disease affecting seven million people. The disease cycle is maintained between Triatominae insects and Mammalia hosts; a refractory effect against infection was noted in birds, but only verified in poultry. This paper presents a new host record for T. cruzi, the American barn-owl (Tyto furcata). Trypanosoma cruzi DTU II molecular evidence was found in heart, intestine, liver, and breast suggesting an established chronic infection based on the parasite DNA presence in multiple organs but absent in spleen, as in the murine model and chronically infected raccoons (Procyon lotor). For birds, the parasite rejection was explained based on the complement and high body temperature, but these mechanisms vary greatly among the members of the avian class. Therefore, there is a need to investigate whether more bird species can become infected, and if T. furcata has a role in disseminating, transmitting and/or maintaining the parasite.

5 January 2017 in PLOS ONE
Verified
Journal Article
Open access
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CVClaudia Villanueva-Garcia
Claudia Villanueva-Garcia
EGElias Jose Gordillo-Chavez
Elias Jose Gordillo-Chavez
ELEduardo Lopez-Escamilla
Eduardo Lopez-Escamilla
EREmilio Rendon-Franco
Emilio Rendon-Franco
CMClaudia I. Muñoz-García
Claudia I. Muñoz-García
FMFernando Martínez-Hernández
Fernando Martínez-Hernández
Although the presence of cryptic host specificity has been documented in Blastocystis, differences in infection rates and high genetic polymorphism within and between populations of some subtypes (ST) have impeded the clarification of the generalist or specialist specificity of this parasite. We assessed the genetic variability and host specificity of Blastocystis spp. in wild howler monkeys from two rainforest areas in the southeastern region of Mexico. Fecal samples of 225 Alouatta palliata (59) and A. pigra (166) monkeys, belonging to 16 sylvatic sites, were analyzed for infection with Blastocystis ST using a region of the small subunit rDNA (SSUrDNA) gene as a marker. Phylogenetic and genetic diversity analyses were performed according to the geographic areas where the monkeys were found. Blastocystis ST2 was the most abundant (91.9%), followed by ST1 and ST8 with 4.6% and 3.5%, respectively; no association between Blastocystis ST and Alouatta species was observed. SSUrDNA sequences in GenBank from human and non-human primates (NHP) were used as ST references and included in population analyses. The haplotype network trees exhibited different distributions: ST1 showed a generalist profile since several haplotypes from different animals were homogeneously distributed with few mutational changes. For ST2, a major dispersion center grouped the Mexican samples, and high mutational differences were observed between NHP. Furthermore, nucleotide and haplotype diversity values, as well as migration and genetic differentiation indexes, showed contrasting values for ST1 and ST2. These data suggest that ST1 populations are only minimally differentiated, while ST2 populations in humans are highly differentiated from those of NHP. The host generalist and specialist specificities exhibited by ST1 and ST2 Blastocystis populations indicate distinct adaptation processes. Because ST1 exhibits a generalist profile, this haplotype can be considered a metapopulation; in contrast, ST2 exists as a set of local populations with preferences for either humans or NHP.

29 August 2014 in Parasites & Vectors
Verified
Journal Article
Open access
PDF file
FMFernando Martínez-Hernández
Fernando Martínez-Hernández
EREmilio Rendon-Franco
Emilio Rendon-Franco
LGLilia Gama
Lilia Gama
CVClaudia Villanueva-García
Claudia Villanueva-García
MRMirza Romero-Valdovinos
Mirza Romero-Valdovinos
GVGuiehdani Villalobos
Guiehdani Villalobos
A large variety of mammals act as natural reservoirs of Trypanosoma cruzi (the causal agent of Chagas disease) across the American continent. Related issues are infection and parasite burden in these reservoirs, and whether they are able to control T. cruzi infections. These parameters can indicate the real role of mammals as T. cruzi reservoirs and transmitters. Here, two species of mammals, white-nosed coati (Nasua narica) and raccoon (Procyon lotor), were examined for to determine: a) T. cruzi presence, and; b) their ability to control T. cruzi infection. Multiple capture-recaptures of both species were carried out in semi-wild conditions in Villahermosa, Tabasco, Mexico, for 5 years. Two samplings per year (summer and winter) took place. Prevalence and pattern of T. cruzi infection were determined by PCR from both mammals’ blood samples. Raccoon samples had a higher relative infection values (26.6%) compared to those of white-nosed coati (9.05%), being this difference significant in summer 2012 (P < 0.00001), summer (P = 0.03) and winter 2013 (P = 0.02). Capture and recapture data indicated three infection dynamics: 1) negative–positive-negative infection; 2) positive–negative-positive infection; and 3) positive at all sampling times. These results indicate that both coati and raccoons may be able to control T. cruzi infection. Thus, the role as efficient reservoirs could be questioned (at least for those times when mammals are able to tolerate the infection). However, while infected, they may also be able to approach human dwellings and play a role important in linking sylvatic and domestic cycles.