Molecular identification of Trypanosoma theileri (Laveran, 1902) in cattle from two slaughterhouses in Ecuador and its relation with other haemotropic agents.

Trypanosoma theileri is a worldwide distributed haemoparasite that has been reported throughout the American continent in various species, including bovines, buffaloes and bats. In bovines, high incidence of T. theileri can be harmful when associated with other infections or under stress situations. There is little information on this hemoflagellate in Ecuador, which prompted the study and molecular identification of the trypanosomes collected in two slaughtering centers. Between February and April 2021, a total of 218 samples of bovine blood were collected in abattoirs located in the Andean region of Quito (n = 83) and in the coastal region, in Santo Domingo (n = 135). Quito public Slaughterhouse is the biggest in Ecuador, and for that, they receive animals from all country; on the other hand, Santo Domingo's Slaughterhouse is a small one where mainly females from the region are sacrificed and some males. The samples were evaluated using two molecular tests, the PCR cathepsin L-like (CatL) specific for T. theileri and for the positive samples, a Nested PCR that targets the ITS of the 18S gene. The corresponding PCR products were sequenced, analyzed by BLAST/NCBI and the sequences were used to build a concatenated phylogenetic tree, using the MEGA XI software. Overall, 34 out of the 218 samples, (15.6%) were positive to T. theileri by PCR CatL, resulting from 20/83 (24.1%) positives from the Quito abattoir and 14/135 (10.4%) from the Santo Domingo slaughterhouse. These prevalence rates were found to be significantly different (p = 0.006). According to the phylogenetic tree based on the CatL and ITS concatenated sequences (n = 13), the two novel Equatorial T. theileri isolates, ThI (n = 7) and ThII (n = 6) are closely related and associated to the IC, IB and IIB genotypes, present in Brazil, Venezuela and Colombia. Thirty-one out of the thirty-four T. theileri-positive bovines were co-infected with other haemotropic pathogens, Anaplasma marginale Babesia spp and T. vivax. This coinfection could be responsible for additional pathologies and harmful effects on the affected cattle. This study presents the molecular identification and genotypification of T. theileri isolated from cattle in Ecuador through the analysis of CAtL and ITS sequences, and the high frequency of coinfection of this hemoflagellate with other blood haemotropic organisms.

Detection of Babesia spp. in High Altitude Cattle in Ecuador, Possible Evidence of the Adaptation of Vectors and Diseases to New Climatic Conditions.

BACKGROUND: Babesia species are intraerythrocytic protozoa, distributed in tropical and subtropical areas of the world, causing anemic diseases in many animals, including cattle. This disease, called babesisosis, is transmitted from one animal to another through ticks (Tick Borne-Disease or TBD). On the other hand, Ecuador has a tropical climate that allows the development of the vector Rhipicephalus microplus, and therefore favors the transmission of Babesia spp. in cattle. METHODS AND PRINCIPAL FINDINGS: We determined the presence of Babesia spp. by PCR using 18s ribosomal gene as target (18s PCR) in 20 farms in the area of El Carmen (zone below 300 m above sea level) and 1 farm in Quito (2469 m.a.s.l.). In addition, we analyzed parameters such as age, sex, and packed cell volume (PCV) as explanatory variable associated with the disease. RESULTS: The 18s PCR test showed that 18.94% (14.77% Babesia bovis and 4.17% Babesia bigemina) and 20.28% (14.69% B. bovis and 5.59% B. bigemina) of the cattle were positive for Babesia spp in farms sampled in El Carmen and in Quito, respectively. Age influenced the presence of animals positive for Babesia spp., but sex and PCV did not. The phylogenetic analysis of sequences showed 4 isolates of B. bovis and 3 isolates of B. bigemina in the 2 study zones, with similarities between 99.73 and 100% with other sequences. One B. bovis isolate was similar in the zone of El Carmen and Quito. CONCLUSION AND SIGNIFICANCE: This work is the first molecular characterization of B. bigemina and B. bovis in Ecuador, and it is also the first evidence of Babesia spp. in cattle in the area of Quito at an altitude of 2469 m.a.s.l., being the highest altitude reported for animals with babesiosis and for the tick R. microplus. Climatic factors as well as mobility of tick-carrying animals without any control allow the presence of Babesiosis outbreaks in new geographical areas.

First report and molecular identification of Trypanosoma (Duttonella) vivax outbreak in cattle population from Ecuador.

The bovine trypanosomosis is responsible for economic losses from tropical and subtropical areas of Africa and Latin America. This disease is characterized by fever, anaemia, loss of production and even death. Few studies have been carried out in Ecuador regarding Trypanosoma spp. presence but the species has not been determined in cattle and those have only determined the presence of genus, but not the species. The aim of this study was to identify and characterize the trypanosome species involved in the suspected bovine trypanosomosis outbreak reported in Convento Village in Manabí Province located in the coastal region of Ecuador. Twenty cattle from three farms were sampled. Three samples were positive for T. vivax, using an end-point polymerase chain reaction (PCR) to amplify a fragment of the cathepsin L-like cysteine protease (CatL-like) gene. A phylogenetic tree analysis of these three Ecuadorian isolates showed a close relationship with isolates from South America (Colombia, Brazil and Venezuela) and West Africa (Nigeria). This is the first report of T. vivax in Ecuadorian cattle.

Serological evidence of Coxiella burnetii infection in cattle and farm workers: is Q fever an underreported zoonotic disease in Ecuador?

Background: Q fever is an underreported zoonotic disease of cattle and men in most countries of the world. Very little information about the prevalence of Coxiella burnetii infection in animals and humans comes from South and Central America and systematic studies are lacking. Methods: A seroprevalence survey for Q fever amongst cattle, farm workers and students was conducted in Ecuador using a commercial ELISA kit. Results: Survey results showed an unexpectedly high prevalence of Coxiella burnetii antibodies in dairy cattle (43%) and in farm workers (34%). In addition, a clinical case in a human of acute Q fever in the convalescent stage was detected. Conclusion: We conclude that the disease is endemic in Ecuador but is overlooked by medical and laboratory personnel. Q fever should be considered a public health issue in Ecuador and further research into the clinical relevance of this infection is recommended.

Parasitological, Hematological, and Immunological Response of Experimentally Infected Sheep with Venezuelan Isolates of Trypanosoma evansi, Trypanosoma equiperdum, and Trypanosoma vivax.

There are three trypanosoma species of veterinary importance in South America: (1) Trypanosoma evansi, the causative agent of derrengadera mechanically transmitted by bloodsucking insects such as tabanids, (2) Trypanosoma vivax, also mechanically transmitted by some dipteras hematophages as tabanids and/or Stomoxys, and (3) T. equiperdum, a tissue parasite adapted to sexual transmission and the causative agent of dourine, a distinctive disease that affects only Equidae. In order to evaluate the parasitological, hematological, and serological response of sheep infected with T. vivax, T. evansi, and T. equiperdum, four female sheep were experimentally infected with Venezuelan trypanosome field isolates: two T. evansi of differing virulences, one T. equiperdum; one T. vivax. Parasitemia and clinical parameters such as hematocrit, red blood cell count, hemoglobin, and body temperature were measured. T. evansi caused a chronic disease with undulant parasitemia alternating with some cryptic periods of at least 54 days, with no clinical signs. T. equiperdum, never described as infectious to ruminants, also caused a chronic disease with low undulant parasitemia. T. vivax caused an acute infection with severe anemia showing a drop of more than 70% of the hematocrit value, high fever, and rapid deterioration of physical condition, for 36 days of infection. Indirect ELISAs using crude extracts of the three species of trypanosomes as antigens were performed for detection of anti-trypanosome antibodies in sheep sera. Cross-reaction was observed between the three parasite species. These results show that sheep are susceptible to the three-trypanosome species and suggest they can act as a reservoir when sheep are raised and managed with other important livestock such as cattle, horses, buffalos, or goats. These findings are especially interesting for T. equiperdum, a species that has not been reported as infective to sheep.

Trypanosoma vivax infection in sheep: Different patterns of virulence and pathogenicity associated with differentially expressed proteomes.

Cattle trypanosomosis caused by Trypanosoma vivax is a widely distributed disease in Africa and Latin America. It causes significant losses in the livestock industry and is characterized by fluctuating parasitemia, anemia, fever, lethargy, and weight loss. In this study we evaluated the virulence (capacity to multiply inside the host and to modulate the host response) and pathogenicity (ability to produce disease and/or mortality) patterns of two T. vivax strains (TvMT1 and TvLIEM176) in experimentally-infected sheep and determined the proteins differentially expressed in the proteomes of these two strains. Hematological and clinical parameters were monitored in experimentally-infected versus non-infected sheep for 60 days. All the infected animals developed discernable parasitemia at 3 days post-infection (dpi), and the first parasitemia peak was observed at 6 dpi. The maximum average value of parasitemia was 1.3×107 (95% CI, 7.9×105-2×108) parasites/ml in TvLIEM176-infected animals, and 2.5×106 (95% CI, 1.6×105-4×107) parasites/ml in TvMT1-infected ones. Anemia and clinical manifestations were more severe in the animals infected by TvMT1 strain than in those infected by TvLIEM176. In the proteomic analysis, a total of 29 proteins were identified, of which 14 exhibited significant differences in their expression levels between strains. Proteins with higher expression in TvLIEM176 were: alpha tubulin, beta tubulin, arginine kinase, glucose-regulated protein 78, paraflagellar protein 3, and T-complex protein 1 subunit theta. Proteins with higher expression in TvMT1 were: chaperonin HSP60, T-complex protein 1 subunit alpha, heat shock protein 70, pyruvate kinase, glycerol kinase, inosine-5'-monophosphate dehydrogenase, 73kDa paraflagellar rod protein, and vacuolar ATP synthase. There was a difference in the virulence and pathogenicity between the T. vivax strains: TvLIEM176 showed high virulence and moderate pathogenicity, whereas TvMT1 showed low virulence and high pathogenicity. The proteins identified in this study are discussed for their potential involvement in strains' virulence and pathogenicity, to be further defined as biomarkers of severity in T. vivax infections.

Trypanosoma vivax infection in sheep: Different patterns of virulence and pathogenicity associated with differentially expressed proteomes.

Cattle trypanosomosis caused by Trypanosoma vivax is a widely distributed disease in Africa and Latin America. It causes significant losses in the livestock industry and is characterized by fluctuating parasitemia, anemia, fever, lethargy, and weight loss. In this study we evaluated the virulence (capacity to multiply inside the host and to modulate the host response) and pathogenicity (ability to produce disease and/or mortality) patterns of two T. vivax strains (TvMT1 and TvLIEM176) in experimentally-infected sheep and determined the proteins differentially expressed in the proteomes of these two strains. Hematological and clinical parameters were monitored in experimentally-infected versus non-infected sheep for 60 days. All the infected animals developed discernable parasitemia at 3 days post-infection (dpi), and the first parasitemia peak was observed at 6 dpi. The maximum average value of parasitemia was 1.3 × 107 (95% CI, 7.9 × 105-2 × 108) parasites/ml in TvLIEM176-infected animals, and 2.5 × 106 (95% CI, 1.6 × 105-4 × 107) parasites/ml in TvMT1-infected ones. Anemia and clinical manifestations were more severe in the animals infected by TvMT1 strain than in those infected by TvLIEM176. In the proteomic analysis, a total of 29 proteins were identified, of which 14 exhibited significant differences in their expression levels between strains. Proteins with higher expression in TvLIEM176 were: alpha tubulin, beta tubulin, arginine kinase, glucose-regulated protein 78, paraflagellar protein 3, and T-complex protein 1 subunit theta. Proteins with higher expression in TvMT1 were: chaperonin HSP60, T-complex protein 1 subunit alpha, heat shock protein 70, pyruvate kinase, glycerol kinase, inosine-5'-monophosphate dehydrogenase, 73 kDa paraflagellar rod protein, and vacuolar ATP synthase. There was a difference in the virulence and pathogenicity between the T. vivax strains: TvLIEM176 showed high virulence and moderate pathogenicity, whereas TvMT1 showed low virulence and high pathogenicity. The proteins identified in this study are discussed for their potential involvement in strains' virulence and pathogenicity, to be further defined as biomarkers of severity in T. vivax infections.

PCR-diagnosis of Anaplasma marginale in cattle populations of Ecuador and its molecular identification through sequencing of ribosomal 16S fragments.

BACKGROUND: Bovine anaplasmosis is an endemic disease in tropical and subtropical areas. It is caused by a bacterium named Anaplasma marginale, and represents an economic problem for cattle farmers due to the losses it generates, such as: mortalities, reduced production, quarantine measures, treatments and control of vectors. The method most often used to diagnose this haemotrophic bacterium is direct examination on blood smear, which sensitivity and specificity are limited compared to other methods such as PCR. The present study aimed at investigating the presence of A. marginale in dairy cattle of Luz de América commune, province of Santo Domingo de los Tsachilas. Two PCRs were used to amplify specific regions of the Rickettsia for its molecular identification. RESULTS: At first, 151 blood samples were tested: msp5 specific gene of A. marginale was identified in 130 samples, meaning 86.1% of them were infected by the rickettsia. Two positive samples were further randomly selected to confirm the presence of A. marginale through amplification, cloning and sequencing of the conserved region of gene 16S rRNA. The analysis of sequences obtained through cloning revealed a 100% identity between both samples and those registered in GenBank for A. marginale. CONCLUSION: This is the first report and molecular identification of A. marginale in the bovine population of Ecuador and its prevalence was high at the level of farms and animals. These results demonstrate the importance of proceeding to evaluate and characterize bovine Anaplasmosis in Ecuador in order to establish control measures and reduce their impact.

Trypanosoma vivax Adhesion to Red Blood Cells in Experimentally Infected Sheep.

Trypanosomosis, a globally occurring parasitic disease, poses as a major obstacle to livestock production in tropical and subtropical regions resulting in tangible economic losses. In Latin America including Venezuela, trypanosomosis of ruminants is mainly caused by Trypanosoma vivax. Biologically active substances produced from trypanosomes, as well as host-trypanosome cellular interactions, contribute to the pathogenesis of anemia in an infection. The aim of this study was to examine with a scanning electron microscope the cellular interactions and alterations in ovine red blood cells (RBC) experimentally infected with T. vivax. Ovine infection resulted in changes of RBC shape as well as the formation of surface holes or vesicles. A frequent observation was the adhesion to the ovine RBC by the trypanosome's free flagellum, cell body, or attached flagellum in a process mediated by the filopodia emission from the trypanosome surface. The observed RBC alterations are caused by mechanical and biochemical damage from host-parasite interactions occurring in the bloodstream. The altered erythrocytes are prone to mononuclear phagocytic removal contributing to the hematocrit decrease during infection.

Kinetoplast adaptations in American strains from Trypanosoma vivax.

The mitochondrion role changes during the digenetic life cycle of African trypanosomes. Owing to the low abundance of glucose in the insect vector (tsetse flies) the parasites are dependent upon a fully functional mitochondrion, capable of performing oxidative phosphorylation. Nevertheless, inside the mammalian host (bloodstream forms), which is rich in nutrients, parasite proliferation relies on glycolysis, and the mitochondrion is partially redundant. In this work we perform a comparative study of the mitochondrial genome (kinetoplast) in different strains of Trypanosoma vivax. The comparison was conducted between a West African strain that goes through a complete life cycle and two American strains that are mechanically transmitted (by different vectors) and remain as bloodstream forms only. It was found that while the African strain has a complete and apparently fully functional kinetoplast, the American T. vivax strains have undergone a drastic process of mitochondrial genome degradation, in spite of the recent introduction of these parasites in America. Many of their genes exhibit different types of mutations that are disruptive of function such as major deletions, frameshift causing indels and missense mutations. Moreover, all but three genes (A6-ATPase, RPS12 and MURF2) are not edited in the American strains, whereas editing takes place normally in all (editable) genes from the African strain. Two of these genes, A6-ATPase and RPS12, are known to play an essential function during bloodstream stage. Analysis of the minicircle population shows that its diversity has been greatly reduced, remaining mostly those minicircles that carry guide RNAs necessary for the editing of A6-ATPase and RPS12. The fact that these two genes remain functioning normally, as opposed to that reported in Trypanosoma brucei-like trypanosomes that restrict their life cycle to the bloodstream forms, along with other differences, is indicative that the American T. vivax strains are following a novel evolutionary pathway.

Mecanismos de Variación Antigénica en Anaplasma marginale / Mechanisms of Antigenic Variation in Anaplasma marginale

Anaplasma marginale (A. marginale), es una bacteria del orden de las Rickettsias que ocasiona la anaplasmosis bovina en regiones tropicales y subtropicales del mundo. Esta enfermedad, trasmitida principalmente por tábanos y garrapatas, se desarrolla típicamente en una etapa inicial aguda con manifestaciones clínicas caracterizadas principalmente por anemia y fiebre. Después de un par de meses, los animales recuperan su condición física y se hacen asintomáticos, siendo incapaces de eliminar completamente la bacteria, convirtiéndose en animales persistentemente infectados. Esto se debe a la capacidad de A. marginale para evadir el sistema inmune. En este sentido, se ha demostrado la existencia de un mecanismo de variación antigénica en las proteínas MSP1, MSP2 y MSP3 de la bacteria. Al evaluar la familia multigénica que codifica para la MSP2, se determinó que está conformada por dos regiones conservadas que flanquean una región central hipervariable. De esta manera, al expresarse cada una de las 52 variables de la MSP2, se expresa un epítope diferente. Cuando se describió el genoma completo de este hemotrópico, se encontró también la presencia de 16 pseudogenes msp2, los cuales pueden ser recombinados dentro del sitio de expresión del operón de la MSP2, constituyendo un segundo mecanismo de variación. Además de ello, los fragmentos hipervaribles y los pseudogenes se pueden combinar entre sí, en un proceso denominado conversión génica, creando nuevos epítopes “recombinantes”, confiriendo una capacidad de variabilidad antigénica casi infinita al A. marginale (tercer mecanismo). Un cuarto mecanismo de variación antigénica, lo constituye la dimerización de la MSP2 sobre la superficie del A. marginale, debido a que la expresión simultánea de variantes conforman epítopes únicos. En conclusión, la recombinación génica de la MSP2 y su dimerización en la membrana, constituye un mecanismo muy eficiente de variación antigénica para eludir el sistema inmunológico del hospedador.

Anaplasma marginale (A. marginale) is a bacterium of the Rickettsiales order that causes bovine anaplasmosis in tropical and subtropical regions worldwide. This disease, mainly transmitted by ticks and horseflies, typically develops in an initial acute stage, with clinical signs characterized by anemia and fever. After two months, animals recover their original physical condition and become asymptomatic, being unable to completely eliminate the bacterium, turning into persistently infected animals. This is due to the ability of A.marginale to evade the immune system. In this regard, the existence of a mechanism for antigenic variation in proteins of the bacterium, such as MSP1, MSP2, and MSP3, has been demonstrated. When assessing the multigenic family which encodes for MSP2, it was determined that it consists of two conserved regions flanking a central hypervariable region. Thus, when expressing each of the 52 MSP2 variables, a different epitope is also expressed. When the entire genome of this parasite was decoded, the presence of 16 pseudogenes for MSP2 was also discovered. These pseudogenes can be recombined within the operon expression site of MSP2, providing a second mechanism of variation. Moreover, both the hypervariable fragments and pseudogenes can combine among them, in a process called gene conversion, creating new “recombinant” epitopes, conferring the A. marginale with an almost infinite capacity for antigenic variability (third mechanism). A fourth mechanism of antigentic variation consists of the dimerization of MSP2 on the surface of A. marginale, because the simultaneous expression of variants creates unique epitopes. In conclusion, gene recombination of MSP2 along with the dimerization of MSP2 on the membrane provides a very efficient mechanism for antigenic variation for evading the host’s immune system.

Morfometría Comparativa de Cinco Aislados Venezolanos Trypanosoma vivax / Comparative Morfometric of five Venezuelan Trypanosoma vivax isolates

La tripanosomosis causada por Trypanosoma vivax, se encuentra distribuida en las regiones tropicales y subtropicales de África, América Latina y Asia, causando grandes pérdidas económicas. Los análisis biométricos previos reportan que T. vivax mide entre 18 y 31 µm; sin embargo, pocos estudios de este tipo se han realizado en Venezuela. El objetivo del presente estudio fue describir y comparar la morfometría de cinco aislados de T. vivax, con el propósito de demostrar la variabilidad en el tamaño de los protozoarios obtenidos a partir de bovinos con infecciones activas en diferentes zonas geográficas del país. Para ello, se realizaron infecciones experimentales en ovinos y se tomaron muestras de sangre en el primer pico de parasitemia. Se registraron microfotografías de los estadios hematozoicos (20 micrografías de microscopia electrónica de barrido) de cada aislado para estudios morfológicos. Los resultados revelaron diferencias significativas (p<0,05); (p<0,01) en la longitud entre los aislados. Los valores totales promedios fueron: 20,99 ± 2,10 µm, con variaciones medias entre 18,12 ± 4,42 µm en los de menor tamaño y 24,35 ± 5,55 µm en la mayor longitud, respectivamente. Por lo tanto, se demostró la existencia de variabilidad en el tamaño de estos hemoparásitos de Venezuela.

Trypanosomosis caused by Trypanosoma vivax (T. vivax), is distributed in tropical and subtropical regions of Africa, Latin America and Asia, causing great economic losses. Previous biometric analysis report that T. vivax measures between 18 and 31 µm; but few such studies have been conducted in Venezuela. The aim of this study was to describe and compare the morphometry of five isolates of T. vivax, to demonstrate the variability in size of the protozoa obtained from naturally-infected cattle in different geographical areas of Venezuela. To accomplish this, experimental infections were induced in sheep and blood samples were taken at the first peak of parasitemia. Micrographs of stages of hematozoa (20 micrographs of each specimen using scanning electron microscopy) were recorded for morphological studies. The results of this research revealed significant (p<0.05); (p<0.01) statistical differences in length among them. The total average length was 20.99 ± 2.10 µm, with variations which ranged from 18.12 ± 4.42 µm, for smaller lengths, and 24.35 ± 5.55 µm, for greater lengths, respectively. Therefore, the existence of variability in the size of these hemoparasites in Venezuela was demonstrated.

A proline racemase based PCR for identification of Trypanosoma vivax in cattle blood.

A study was conducted to develop a Trypanosoma vivax (T. vivax) specific PCR based on the T. vivax proline racemase (TvPRAC) gene. Forward and reverse primers were designed that bind at 764-783 bp and 983-1002 bp of the gene. To assess its specificity, TvPRAC PCR was conducted on DNA extracted from different haemotropic pathogens: T. vivax from Nigeria, Ethiopia and Venezuela, T. congolense Savannah type, T. brucei brucei, T. evansi, T. equiperdum, T. theileri, Theileria parva, Anaplasma marginale, Babesia bovis and Babesia bigemina and from bovine, goat, mouse, camel and human blood. The analytical sensitivity of the TvPRAC PCR was compared with that of the ITS-1 PCR and the 18S PCR-RFLP on a dilution series of T. vivax DNA in water. The diagnostic performance of the three PCRs was compared on 411 Ethiopian bovine blood specimens collected in a former study. TvPRAC PCR proved to be fully specific for T. vivax, irrespective of its geographical origin. Its analytical sensitivity was lower than that of ITS-1 PCR. On these bovine specimens, TvPRAC PCR detected 8.3% T. vivax infections while ITS-1 PCR and 18S PCR-RFLP detected respectively 22.6 and 6.1% T. vivax infections. The study demonstrates that a proline racemase based PCR could be used, preferably in combination with ITS-1 PCR, as a species-specific diagnostic test for T. vivax infections worldwide.

Prevalencia de trypanosoma spp. mediante ELISA e inmunofluorescencia indirecta en tres rebaños de búfalos de agua del estado Cojedes, Venezuela / Prevalence of trypanosoma spp. by ELISA and indirect fluorescent antibody test in three water buffaloes herds from the State of Cojedes, Venezuela

Animal trypanosomiasis is a disease caused by parasites of the genus Trypanosome. This malady is widely distributed in many countries, located in tropical and subtropical areas of the world where blood-sucking flies are present. Water buffaloes are important domestic animals used for meat and milk production, and draught power. Buffalo herds are raised in areas where trypanosomiasis is endemic. In Venezuela, the buffalo industry is becoming a very important and common livestock. However, animals imported from non-endemic areas may suffer severe infections. The development of methods which ensure an efficient epidemiological surveillance against this disease is of great relevance. The immunological tests are of great importance for this purpose, because of the low sensitivity of the current parasitological methods, due to the low parasite burden that occur in subclinical and chronic infections caused by trypanosomes. To estimate the serological prevalence of trypanosome in water buffaloes, an enzyme-linked immunosorbent assay (ELISA) was used in buffalo samples of healthy animals from the municipalities of Rómulo Gallegos, Ricaurte and Girardot, in the State of Cojedes, Venezuela. Additionally, samples were also assessed with the indirect fluorescence antibody test (IFAT) and the microhematocrit test (MHCT). A total of 180 blood samples, none of which had an active parasitemia by TMC, were assessed. The prevalence determined by ELISA was 45.56%, which was significantly (P<0.05) higher than that obtained by IFAT (28.89%). The results of the experiments showed a moderate Kappa index of concordance of 0.45 (95% CI: 0.31-0.58); whereas the concordance value for both tests was 73.33%. Both the sensitivity and specificity of ELISA, compared to the IFAT, was 82.69% and 69.53%, respectively. The predictive positive and negative values were 52.44% and 90.82%, respectively. The findings suggest an endemic condition, with moderate infection values caused by Trypanosoma spp. in buffaloes from these regions of Venezuela and show, for the first time, the usefulness of ELISA for epidemiological studies of trypanosomiasis.

Transcriptome analysis of the bloodstream stage from the parasite Trypanosoma vivax.

BACKGROUND: Trypanosoma vivax is the earliest branching African trypanosome. This crucial phylogenetic position makes T. vivax a fascinating model to tackle fundamental questions concerning the origin and evolution of several features that characterize African trypanosomes, such as the Variant Surface Glycoproteins (VSGs) upon which antibody clearing and antigenic variation are based. Other features like gene content and trans-splicing patterns are worth analyzing in this species for comparative purposes. RESULTS: We present a RNA-seq analysis of the bloodstream stage of T. vivax from data obtained using two complementary sequencing technologies (454 Titanium and Illumina). Assembly of 454 reads yielded 13385 contigs corresponding to proteins coding genes (7800 of which were identified). These sequences, their annotation and other features are available through an online database presented herein. Among these sequences, about 1000 were found to be species specific and 50 exclusive of the T. vivax strain analyzed here. Expression patterns and levels were determined for VSGs and the remaining genes. Interestingly, VSG expression level, although being high, is considerably lower than in Trypanosoma brucei. Indeed, the comparison of surface protein composition between both African trypanosomes (as inferred from RNA-seq data), shows that they are substantially different, being VSG absolutely predominant in T. brucei, while in T. vivax it represents only about 55%. This raises the question concerning the protective role of VSGs in T. vivax, hence their ancestral role in immune evasion.It was also found that around 600 genes have their unique (or main) trans-splice site very close (sometimes immediately before) the start codon. Gene Ontology analysis shows that this group is enriched in proteins related to the translation machinery (e.g. ribosomal proteins, elongation factors). CONCLUSIONS: This is the first RNA-seq data study in trypanosomes outside the model species T. brucei, hence it provides the possibility to conduct comparisons that allow drawing evolutionary and functional inferences. This analysis also provides several insights on the expression patterns and levels of protein coding sequences (such as VSG gene expression), trans-splicing, codon patterns and regulatory mechanisms. An online T. vivax RNA-seq database described herein could be a useful tool for parasitologists working with trypanosomes.

Serological evidence of Anaplasma spp. in small ruminants from Venezuela using recombinant MSP5 in immunoenzymatic assay / Evidencia serológica de Anaplasma spp. en pequeños rumiantes de Venezuela utilizando MSP5 recombinante en ensayos inmunoenzimáticos

Anaplasma marginale causes a disease in cattle characterized by fever, anemia and decrease in milk and meat production. Small ruminants do not show signs of disease when infected, but it has been suggested they could act as reservoirs. Goat and sheep breeding is socially and economically important in arid and semi-arid areas in Venezuela, and these species often share space and food with cattle. The aim of this work was to detect antibodies against Anaplasma spp. in Venezuelan goat and sheep flocks. To accomplish this goal, an indirect ELISA using recombinant MSP5 as antigen of A. marginale was performed. Sera obtained from experimental infection in goat and a hyperimmune sheep serum were used as positive controls. Blood sera were obtained from 45 sheep and 48 goats located in Guárico State, an endemic area to bovine anaplasmosis. After standardization of assay for each species, 80.46% of the sheep and 59.25% of the goat sera showed to have antibodies against MSP5. No signs of clinical disease were detected in sampled animals. These results suggest that small ruminants could harbour A. marginale and consequently may be reservoirs for neighbouring cattle if appropriate vectors are present. The development of clinical diseases caused by A. marginale under stress situations and the existence of other Anaplasma species (e.g. A. ovis) in small ruminants should also be investigated.

Anaplasma marginale ocasiona una enfermedad en los bovinos caracterizada por fiebre, anemia y disminución de la producción de leche y carne. Los pequeños rumiantes generalmente no muestran signos clínicos, por lo que pudieran actuar como reservorio. En Venezuela, los ovinos y caprinos tienen gran importancia económica y socialmente en zonas áridas y semi- áridas e incluso, en muchas ocasiones comparten su espacio y alimento con los bovinos. El objetivo de este trabajo fue detectar anticuerpos contra Anaplasma spp. en rebaños de ovinos y caprinos. Para ello, se estandarizó un ELISA indirecto con la MSP5 recombinante de A. marginale, empleando sueros provenientes de infecciones experimentales en caprinos y un suero hiperinmune ovino como controles positivos. Posteriormente, fueron obtenidos sueros sanguíneos de 45 ovinos y 48 caprinos localizados en una zona endémica a anaplasmosis bovina del estado Guárico. De estos, 80,46% de los ovinos y 59,25% de los caprinos presentaron anticuerpos que reconocieron la MSP5, sin embargo, ninguno de estos animales positivos presentaron signos clínicos de la enfermedad. Estos resultados sugieren que los pequeños rumiantes son portadores de A. marginale y por ende, pueden estar actuando como reservorio de la enfermedad para los bovinos en el caso que se encuentren los vectores apropiados. Por lo tanto, se debe profundizar en los estudios sobre el desarrollo de sintomatología clínica en condiciones de estrés y la existencia de otras especies de Anaplasma (como A. ovis) en los ovinos y caprinos de Venezuela.

Tiempo de supervivencia in vivo y criopreservación de Trypanosoma vivax / In vivo survival time and cryopreservation of Trypanosoma vivax

Uno de los problemas más comunes del trabajo con Trypanosoma vivax, es la supervivencia y criopreservación de este protozoario, lo cual origina pérdida de aislados de campo y errores en exámenes parasitológicos. Se propone evaluar la supervivencia in vivo en condiciones de campo y criopreservación de T. vivax. Para determinar la supervivencia, la sangre se sometió a temperatura ambiente y refrigeración a 4°C, luego se determinó la sobrevivencia en el tiempo. Para el estudio de criopreservación, se emplearon dos crioprotectores de diferente naturaleza química: glicerol 10 por ciento y DMSO 5 por ciento de concentración final. Además, la criopreservación se realizó bajo tres condiciones de almacenamiento en nitrógeno líquido: 1) fase gaseosa 2) líquida y 3) combinación de ambas. Durante la evaluación de la supervivencia, se observó que la sobrevivencia de T. vivax en sangre refrigerada disminuyó significativamente (P<0,01), en comparación con aquellas sometidas a temperatura ambiente. Sin embargo, la sobrevivencia de éstos últimos comienza a disminuir luego de 6 horas, aunque algunos hemoparásitos permanecieron viables hasta 24 horas post-recolección. Para evaluar la criopreservación, al cabo de dos semanas, se descongelaron los crioviales, se determinó la sobrevivencia, resultando negativas las muestras sometidas a congelamiento directo en fase líquida. Los otros dos métodos empleados, resultaron similares (estadísticamente no significativos), el glicerol 10 por ciento resultó con mayor número de parásitos viables. En conclusión, se determinó que, las muestras infectadas con T. vivax deben evaluarse antes de 8 horas post-recolección y mantenerlas a temperatura ambiente. Por otra parte, el congelamiento debe realizarse en primera instancia en fase gaseosa o combinación gaseosa/líquida, empleando glicerol 10 por ciento. Estos resultados, permiten sugerir la mejor metodología a ser empleada para la supervivencia de los parásitos antes de exámenes parasitológicos...

One of the common problems working with Trypanosoma vivax is its survival and cryopreservation, which originates loss of field isolates and parasitological examinations mistakes. The aim of this paper was to study the best methodologies for in vivo survival under field conditions and cryopreservation of the T. vivax. In order to study complete blood survival of T. vivax, two surviving conditions were tested at: room temperature and refrigeration at 4°C. The result shows that surviving in cooled sampled diminished significantly (P<0.01) compare with room temperature. Nevertheless, surviving of room temperature parasite begins to diminish after 6 hours, although some parasites remained viable up to 24 hours post-harvesting. Cryopreservation studies were made under three liquid nitrogen storage conditions: 1) gaseous phase 2) liquid and 3) gaseous/ liquid phase combination (glycerol 10 percent and DMSO 5 percent, were used as cryoprotectants). After two weeks and defrost the survive of T. vivax from cryovials determined. The result show that: a) direct freezing in liquid phase samples were negative and b) the other two methodology were positive and statistically similar, glycerol 10 percent resulted with the greatest number of viable parasites. In conclusion, these results suggest that the best methodologies for conservation under field conditions, were that the samples infected with T. vivax must be evaluated before 8 hours post-harvesting at room temperature and cryopreservation condition of the T. vivax, must be made in gaseous phase or gaseous/liquid phase combination.

Evaluación y mejoramiento del ensayo inmunoenzimático (ELISA) para el diagnóstico de la anaplasmosis bovina, utilizando las MSP5 recombinante como antígeno / Evaluation and improvement of an immunoenzimatic assay (ELISA) for diagnosis of bovine anaplasmosis, using recombinant MSP5 as antigen

La anaplasmosis, es una enfermedad producida por la bacteria Anaplasma marginale que está ampliamente distribuida en Venezuela, originando efectos negativos en la salud y productividad de los rebaños bovinos. Hasta el presente se han caracterizado 6 proteínas mayoritarias de superficie (MSP) de esta bacteria, de las cuales la MSP5, ha sido señalada como un excelente polipéptido para el diagnóstico de la enfermedad, debido a que esta proteína es altamente conservada e inmunogénica. Esto ha motivado su clonamiento e inserción en un plásmido de E. coli, para usarla purificada como antígeno en ensayos inmunoenzimáticos. Sin embargo, estudios posteriores, indican que proteínas de E. coli recombinante que eluyen conjuntamente con la MSP5 durante el proceso de purificación, interfieren en el ELISA originando falsos positivos. En el presente trabajo se estandarizó un ELISA indirecto, utilizando la MSP5 como antígeno y se logró disminuir las uniones inespecíficas a las proteínas contaminantes de E. coli, por adición de un suero de conejo anti E. coli que bloquea los epítopes de estas proteínas. A través de un cuadro de contingencia de doble entrada, se determinaron los parámetros de validación del ELISA al compararla con la técnica de naranja de acridina-bromuro de etídio, obteniéndose como resultado que la técnica de ELISA mejorada es 96,1 por ciento sensible, 9 por ciento específica y presenta un valor predictivo del 88,6 por ciento. Además, se estudió una población bovina de 48 mautes de la Estación Experimental La Iguana (estado Guárico), utilizando ambas técnicas, obteniendo una seroprevalencia de 93,7 por ciento por ELISA y una prevalencia de 54,1 por ciento por naranja de acridina-bromuro de etidio. Estos resultados muestran que el bloqueo de los epítopes de las proteínas de E. coli contaminates, utilizando para ello un suero de conejo anti-E. coli, permite disminuir los falsos negativos cuando se utilizan proteínas recombinantes.

Anaplasmosis, is a disease produced by Anaplasma marginale widely distributed in Venezuela, causing negative effects on the health and productivity of bovine herds. Until now, 6 constitutive Anaplasma marginale Mayor Surface Proteins (MSPs) have been characterized, including MSP5 which appears to be an excellent polypeptide for the diagnosis of this disease since it is highly conserved and immunogenic. This has motivated its cloning and insertion into a plasmid in E. coli and the use of the purified antigen in immunoenzymatic assays. However, subsequent indicated that E. coli recombinant proteins, that copurify with MSP5, interfere with the ELISA giving rise to false positives. In the present study, it was accomplished the standardization of an indirect ELISA, using MSP5 as the antigen and it was also diminishing the non-specific unions to the contaminating proteins of E. coli by adding anti-E. coli rabbit serum that blocks the epitopes of these proteins. With the use of a double entry contingency table, the parameters of validation of the ELISA were determined, comparing it to the acridine orange-ethidium bromide technique. The result indicate that the improve MSP5 indirect ELISA has a 96.1% sensitivity, 9% specificity and a predictive value of 88.6%. It was also studied a bovine population of 48 cattle from the Experimental Station “La Iguana” (Guárico State), using both techniques, obtaining a seroprevalence of 93.7% with ELISA and a prevalence of 54.1% with orange acridine-ethidium bromide. These results show that the blockage of the contaminating E. coli protein epitopes using an anti-E. coli rabbit serum permits the diminishment of false negatives when using recombinant proteins.

Assessment of chromogen suitability in ELISA for the detection of anaplasmosis and trypanosomosis.

Two different ELISAs were routinely performed in our laboratory to detect bovine trypanosomosis and anaplasmosis. The ELISA test for trypanosomosis involved the adsorption of a soluble fraction of parasites as the antigen; and, the ELISA for anaplasmosis was performed with a purified recombinant protein MSP5r adsorbed to the plate. With the purpose of assessing the merit of ABTS and TMB, we compared the absorbance obtained from positive and negative control sera from both assays. The results obtained, suggest that TMB is more adequate for recombinant antigens and that ABTS is preferred when partially purified antigenic extracts are used in the ELISA test.

Uso de proteínas como alternativa diagnóstica para discriminar infecciones entre Trypanosoma vivax y Trypanosoma evansi / Use of proteins as diagnostic tool to discriminate between Trypanosoma vivax and Trypanosoma evansi infections

Tripomastigotes sanguícolas de Trypanosoma vivax y Trypanosoma evansi obtenidos de infecciones experimentales en ovejas y ratones respectivamente, fueron utilizados para purificar y caracterizar proteínas citosólicas mediante el método de partición con Tritón X-114. Los resultados revelan diferencias en los patrones proteicos entre las dos especies. Asimismo, las reacciones antigénicas mediante Western blot utilizando suero de animales naturalmente infectados, permitió discriminar las infecciones entre ambos parásitos. Se sugiere la utilización de esta metodología como una prueba diagnóstica confiable.