Angélica Pech May

Dr. Angélica Pech May


Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

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

Representative Publications

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19 May 2010 in Medical and Veterinary Entomology
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Journal Article
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AMAngélica Pech May
Angélica Pech May
Francisco EscobedoFrancisco Escobedo
Francisco Escobedo
MBM. Berzunza‐Cruz
M. Berzunza‐Cruz
ERE. A. Rebollar‐Téllez
E. A. Rebollar‐Téllez
Cutaneous leishmaniasis (CL) is endemic to the Yucatan Peninsula of Mexico. The main causative agent is the parasite Leishmania mexicana (Biagi) (Kinetoplastida: Trypanosomatidae) and, based on the classic work of Dr Biagi's research team, it has been generally accepted and frequently reported that the only vector of L. mexicana in the region is the sandfly Lutzomyia olmeca olmeca (Vargas & Diáz‐Nájera) (Diptera: Psychodidae). Evidence gathered from recent entomological studies conducted mainly in Calakmul, Campeche, however, suggests that other species may also be vectors of L. mexicana . We conducted a field study in two villages in Calakmul, Campeche in the Yucatan Peninsula, where recent cases of CL have been reported, to document the species composition and relative abundances of the sandfly fauna and to identify which species are likely to be the main vectors by assessing the biting rates and parasite infection rates of the suspected vector species. Sandfly catches were conducted from November 2005 to February 2006 in Unión 20 de Junio and Dos Lagunas Sur. Sandflies were captured using Shannon (18.00–22.00 hours), Disney and CDC light traps (18.00–06.00 hours). Biting and infection rates were calculated for the four most abundant species: Lutzomyia cruciata (Coquillett), Lu. o. olmeca , Lutzomyia panamensis (Shannon) and Lutzomyia shannoni (Dyar). In Dos Lagunas Sur, Lu. panamensis and Lu. o. olmeca exhibited the highest biting rates throughout the sampling period. In Unión 20 de Junio, Lu. cruciata and Lu. o. olmeca had the highest biting rates over the same period. Regarding infection rates, we report herein the establishment of a polymerase chain reaction protocol and validation of IR1 and LM17 oligonucleotides to analyse the infection rates of sandflies. Out of 769 females analysed, the overall infection rates were 1.4% in Dos Lagunas Sur and 5.3% in Unión 20 de Junio. In Dos Lagunas Sur we found L. mexicana infections in two sandfly species, Lu. shannoni and Lutzomyia ylephiletor (Fairchild & Hertig), whereas in Unión 20 de Junio we found infections in Lu. shannoni , Lu. cruciata , Lu. o. olmeca and Lu. panamensis . The possible role of these four sandfly species in relation to L. mexicana transmission in Calakmul is discussed.

1 November 2015 in Acta Tropica
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SLSury Antonio López-Cancino
Sury Antonio López-Cancino
ETEzequiel Tun-Ku
Ezequiel Tun-Ku
HCHimmler Keynes De la Cruz-Felix
Himmler Keynes De la Cruz-Felix
CICarlos Ibarra-Cerdeña
Carlos Ibarra-Cerdeña
AIAmaia Izeta-Alberdi
Amaia Izeta-Alberdi
JRJanine Ramsey
Janine Ramsey

1 September 2017 in International Journal for Parasitology
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Journal Article
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APA. Townsend Peterson
A. Townsend Peterson
LCLindsay P. Campbell
Lindsay P. Campbell
DMDavid A. Moo-Llanes
David A. Moo-Llanes
BTBruno Travi
Bruno Travi
CGCamila González
Camila González
JSJeffrey J. Shaw
Jeffrey J. Shaw

28 January 2019 in PLOS Neglected Tropical Diseases
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AMAngélica Pech May
Angélica Pech May
CMCarlos Jesús Mazariegos-Hidalgo
Carlos Jesús Mazariegos-Hidalgo
AIAmaia Izeta-Alberdi
Amaia Izeta-Alberdi
SLSury Antonio López-Cancino
Sury Antonio López-Cancino
ETEzequiel Tun-Ku
Ezequiel Tun-Ku
JRJanine M Ramsey
Janine M Ramsey
The population genetics of Triatoma dimidiata haplogroups was analyzed at landscape and sub-regional scales in Chiapas and regional level across the Mexican Neotropics, and phylogeography of the complex was re-analyzed across its complete geographic range. Two contiguous fragments of the ND4 gene were analyzed due to bias from differential haplogroup specificity using a previously designed sequence. At both landscape (anthropic modification gradient) and regional (demographic, fragmentation, biogeographic, climate) scales, lowest T. dimidiata genetic diversity occurs where there is greatest historical anthropic modification, and where T. cruzi infection prevalence is significantly highest. Trypanosoma cruzi prevalence was significantly higher than expected in haplogroups 1 and 3, while lower than expected in haplogroup 2. There was also a significant difference of DTUI and DTUVI infection frequencies in both haplogroups 1 and 3, while no difference of either in haplogroup 2. All haplogroups from the Mexican Neotropics had moderate to high haplotype diversity, while greatest genetic differentiation was between haplogroups 1 and 3 (above FST = 0.868, p < 0.0001). Divergence of the complex from the MRCA was estimated between 0.97 MYA (95% HPD interval = 0.55–1.53 MYA) and 0.85 MYA (95% HPD interval = 0.42–1.5 MYA) for ND4A and both concatenated fragments, respectively, with primary divergence from the MRCA of haplogroups 2 and 3. Effective population size for Mexican haplogroups 1 and 2 increased between 0.02 and 0.03 MYA. This study supports previous ecological niche evidence for the complex´s origin surrounding the Tehuantepec Isthmus, and provides evidence for recent divergence of three primary dimidiata haplogroups, with differential T. cruzi infection frequency and DTU specificity, important components of vector capacity. Triatoma dimidiata is one of the broadest distributed triatomine species´ complexes transmitting Trypanosoma cruzi. In Mexico, three haplogroups of the T. dimidiata complex have been reported and all are primary vectors of Chagas disease south of the Tehuantepec Isthmus. Given their epidemiological importance, the question arises whether haplogroups have similar genetic diversity in domestic/modified landscapes, as well as infection characteristics and parasite DTU associations, key components of vector capacity. The aim of the present study was to analyze Triatoma dimidiata population genetics across landscapes, sub-regional, regional, and global Neotropical realm scales, using two contiguous fragments of the ND4 gene. Our results support previous evidence for the complex´s origin surrounding the Tehuantepec Isthmus, and provides evidence for recent divergence of three principal dimidiata haplogroups and significant secondary divergence within each. Differential T. cruzi prevalence and Discrete Typing Unit (DTU) specificity for individual haplogroups provide evidence for potential differential vector capacity within the complex in Mexico.

4 April 2016 in Medical and Veterinary Entomology
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Journal Article
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AMAngélica Pech May
Angélica Pech May
GPG. Peraza‐Herrera
G. Peraza‐Herrera
DMD. A. Moo‐Llanes
D. A. Moo‐Llanes
Francisco EscobedoFrancisco Escobedo
Francisco Escobedo
MBM. Berzunza‐Cruz
M. Berzunza‐Cruz
ERE. A. Rebollar‐Téllez
E. A. Rebollar‐Téllez

5 July 2018 in PLOS Neglected Tropical Diseases
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Journal Article
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AMAngélica Pech May
Angélica Pech May
JRJanine M Ramsey
Janine M Ramsey
RIRaúl E González Ittig
Raúl E González Ittig
MGMagali Giuliani
Magali Giuliani
PBPablo Berrozpe
Pablo Berrozpe
OSOscar D Salomón
Oscar D Salomón
The Lutzomyia longipalpis complex has a wide but discontinuous distribution in Latin America, extending throughout the Neotropical realm between Mexico and northern Argentina and Uruguay. In the Americas, this sandfly is the main vector of Leishmania infantum, the parasite responsible for Visceral Leishmaniasis (VL). The Lu. longipalpis complex consists of at least four sibling species, however, there is no current consensus on the number of haplogroups, or on their divergence. Particularly in Argentina, there have been few genetic analyses of Lu. longipalpis, despite its southern expansion and recent colonization of urban environments. The aim of this study was to analyze the genetic diversity and structure of Lu. longipalpis from Argentina, and to integrate these data to re-evaluate the phylogeography of the Lu. longipalpis complex using mitochondrial markers at a Latin American scale. Genetic diversity was estimated from six sites in Argentina, using a fragment of the ND4 and the 3´ extreme of the cyt b genes. Greatest genetic diversity was found in Tartagal, Santo Tomé and San Ignacio. There was high genetic differentiation of Lu. longipalpis in Argentina using both markers: ND4 (FST = 0.452, p < 0.0001), cyt b (FST = 0.201, p < 0.0001). Genetic and spatial Geneland analyses reveal the existence of two primary genetic clusters in Argentina, cluster 1: Tartagal, Santo Tomé, and San Ignacio; cluster 2: Puerto Iguazú, Clorinda, and Corrientes city. Phylogeographic analyses using ND4 and cyt b gene sequences available in GenBank from diverse geographic sites suggest greater divergence than previously reported. At least eight haplogroups (three of these identified in Argentina), each separated by multiple mutational steps using the ND4, are differentiated across the Neotropical realm. The divergence of the Lu. longipalpis complex from its most recent common ancestor (MRCA) was estimated to have occurred 0.70 MYA (95% HPD interval = 0.48–0.99 MYA). This study provides new evidence supporting two Lu. longipalpis genetic clusters and three of the total eight haplogroups circulating in Argentina. There was a high level of phylogeographic divergence among the eight haplogroups of the Lu. longipalpis complex across the Neotropical realm. These findings suggest the need to analyze vector competence, among other parameters intrinsic to a zoonosis, according to vector haplogroup, and to consider these in the design and surveillance of vector and transmission control strategies. The Lutzomyia longipalpis complex has a wide but discontinuous distribution in Latin America, extending throughout the Neotropical realm between Mexico and northern Argentina and Uruguay. In the Americas, this sandfly is the main vector of Leishmania infantum, the parasite responsible for Visceral Leishmaniasis (VL). The Lu. longipalpis complex is composed of at least four sibling species, although there is no current consensus on the number of haplogroups, or their divergence. In Argentina, little is known about the complex population structure. Therefore, the aim of this study was to analyze the diversity and genetic structure of Lu. longipalpis from Argentina and subsequently to analyze the complex phylogeography at a Latin American scale, using two mitochondrial markers. Greatest genetic diversity was found in Tartagal, Santo Tomé and San Ignacio. Two genetic clusters and three Lu. longipalpis haplogroups were identified from the six sites in Argentina. Phylogeographic analyzes using ND4 and cyt b gene sequences and those from across the Neotropical realm registered in GenBank, suggest greater divergence than previously reported. At least eight haplogroups are differentiated using the ND4, each separated by multiple mutational steps. Lu. longipalpis complex divergence from its most recent common ancestor (MRCA) was estimated at mid Pleistocene, 0.70 MYA (95% HPD interval = 0.48–0.99 MYA).