We propose a taxonomic revision of the dixenous trypanosomatids currently classified as Endotrypanum and Leishmania, including parasites that do not fall within the subgenera L. (Leishmania) and L. (Viannia) related to human leishmaniasis or L. (Sauroleishmania) formed by leishmanias of lizards: L. colombiensis, L. equatorensis, L. herreri, L. hertigi, L. deanei, L. enriettii and L. martiniquensis. The comparison of these species with newly characterized isolates from sloths, porcupines and phlebotomines from central and South America unveiled new genera and subgenera supported by past (RNA PolII gene) and present (V7V8 SSU rRNA, Hsp70 and gGAPDH) phylogenetic analyses of the organisms. The genus Endotrypanum is restricted to Central and South America, comprising isolates from sloths and transmitted by phlebotomines that sporadically infect humans. This genus is the closest to the new genus Porcisia proposed to accommodate the Neotropical porcupine parasites originally described as L. hertigi and L. deanei. A new subgenus Leishmania (Mundinia) is created for the L. enriettii complex that includes L. martiniquensis. The new genus Zelonia harbours trypanosomatids from Neotropical hemipterans placed at the edge of the Leishmania-Endotrypanum-Porcisia clade. Finally, attention is drawn to the status of L. siamensis and L. australiensis as nomem nudums.
Background: Blastocystis sp. affects a wide variety of animals and is the most common protozoan in human fecal samples with potential pandemic distribution. In the present study, a systematic review and meta-analysis were conducted to determine the prevalence and distribution of Blastocystis sp. in different classes of hosts in Brazil. Methods: Studies that analyzed hosts of various classes, including humans, domestic animals, wild animals or captive animals, were considered. The pooled prevalence of Blastocystis sp. infection was estimated by random effects models. Results: For humans, similar prevalence rates were found for males (31.0%, 95% CI: 17.0-45.0%; weight 10%) and females (28.0%, 95% CI: 16.0-41.0%; weight 10%); the state of Mato Grosso do Sul showed the highest prevalence, with 41.0% positivity (95% CI: 36.0-46.0%; weight 2.9%). The prevalence among immunocompromised patients was 5.0% (95% CI: 3.0-7.0%; weight 10%), and the most common cause of immunosuppression was hemodialysis, with 23.0% (95% CI: 17.0-29.0%; weight 12.4%). Among classifications according to interaction with humans, wild and domestic animals presented values of 19.0% (95% CI: 7.0-31.0%; weight 42.6%) and 17.0% (95% CI: 13.0-21.0%; weight 29.6%), respectively. Among these animals, mammals (39.0%, 95% CI: 21.0-56.0%; weight 47.3%) and birds (18.0%, 95% CI: 10.0-27.0%; weight 39.3%) exhibited the highest prevalence. Phylogenetic analysis of Blastocystis sp. revealed greater genetic diversity for clades of subtypes (STs) ST1, ST2 and ST3. Conclusions: The overall prevalence of Blastocystis sp. in the Brazilian human population was 24%, which reflects the reality in the South, Southeast and Midwest regions, where prevalence rates of up to 40% were found. Among animals, mammals and birds exhibited the highest prevalence.
O papel do cão como um hospedeiro definitivo de parasitoses intestinais com potencial zoonótico tem sido largamente reconhecido como um problema de saúde pública. Este trabalho analisou a prevalência e distribuição de enteroparasitas em fezes de cães de rua de oito cidades dos diferentes biomas nordestinos, com interesse de investigar a contaminação ambiental por enteroparasitas zoonóticos. 340 amostras fecais foram coletadas nos municípios de João Lisboa e Raposa (Maranhão), Piripiri e Domingos Mourão (Piauí), Fortaleza (Ceará), Petrolina (Pernambuco), Paulo Afonso e Salvador (Bahia). Deste total 43,2% resultaram positivas para alguma espécie de parasita intestinal. Maiores prevalências foram encontradas por ancilostomídeos com 43,5%, seguidos por Toxocara canis com 15%, Neospora sp. com 10,2% e Cryptosporidium sp. com 8,2%. Analisando a porcentagem de positividade por enteroparasitas nos quatro biomas da região Nordeste, o bioma Mata Atlântica foi o que apresentou maior prevalência (54,9%), seguido da Amazônia (54,3%), Caatinga (40,2%) e Cerrado (31,8%). O estudo da ocorrência e distribuição desses parasitas contribui com a vigilância epidemiológica das doenças enteroparasitárias e na aplicação de programas de saúde pública e veterinária para minimizarem a possibilidade de infecção e reinfecção dos animais e a transmissão para seres humanos.
IgM against Mycobacterium leprae may be detected by enzyme-linked immunosorbent assays (ELISAs) based on phenolic glycolipid I (PGL-I) or natural disaccharide octyl bovine serum albumin (ND-O-BSA) as antigens, and the IgG response can be detected by an ELISA based on lipid droplet protein 1 (LID-1). The titers of antibodies against these antigens vary with operational classification. The aim of this study was to compare the accuracy of ELISAs involving PGL-I and ND-O-BSA with that involving LID-1. We included studies that analyze multibacillary and paucibacillary leprosy cases and evaluate the diagnostic accuracy of ELISAs based on LID-1 and/or PGL-I or ND-O-BSA as antigens to measure antibody titers against M. leprae. Studies were found via PubMed, the Virtual Health Library Regional Portal, Literatura Latino-Americana e do Caribe em Ciências da Saúde, Índice Bibliográfico Espanhol de Ciências de Saúde, the Brazilian Society of Dermatology, National Institute for Health and Clinical Excellence, Cochrane Library, Embase (the Elsevier database), and Cumulative Index to Nursing and Allied Health Literature. The Quality Assessment of Diagnostic Accuracy Studies served as a methodological validity tool. Quantitative data were extracted using the Standards for Reporting of Diagnostic Accuracy. Sensitivity, specificity, and a diagnostic odds ratio were calculated, and a hierarchical summary receiver-operating characteristic curve and forest plots were constructed. The protocol register code for this meta-analysis is PROSPERO 2017: CRD42017055983. Nineteen studies were included. ND-O-BSA showed better overall performance in terms of sensitivity, specificity, positive and negative likelihood ratios, and diagnostic odds ratio when compared with PGL-I and LID-1. The multibacillary group showed better performance on these parameters (than the paucibacillary group did), at 94%, 99%, 129, 0.05, and 2293, respectively. LID-1 did not provide any advantage regarding the overall estimate of sensitivity in comparison with PGL-I or ND-O-BSA.
American Tegumentary leishmaniasis (ATL) is an infectious disease caused by
several species of
Leishmania
. Even though the direct
detection of parasites has low sensitivity, it is still the gold standard for
the laboratory diagnosis of ATL. Recent studies have shown promising results of
Enzyme-Linked Immunosorbent Assays
(
ELISAs) using recombinant
antigens. The aim of this study is to compare the accuracy of ELISAs using novel
antigens with the standard ELISA based on soluble antigens of
Leishmania
(SLA) to diagnose ATL. Studies that analyzed
patients with ATL and studies that evaluated the diagnostic accuracy of ELISAs
using novel antigens and SLA were included. The Fourteen studies from PubMed,
Regional Portal of the Virtual Health Library (BVS), Brazilian Society of
Dermatology, Virtual Health Library (IBECS), Literature in the Health Sciences
in Latin America and the Caribbean (LILACS), Medical Literature Analysis and
Retrieval System Online (Medline), Elsevier Embase, Cochrane Library, The
National Institute for Health and Care Excellence (NICE), and Cumulative Index
to Nursing and Allied Health Literature (CINAHL) were included. The novel ELISA
antigens showed a high sensitivity (93.8%-100%) and specificity (82.5-100%), a
better diagnostic performance than SLA-based ELISAs (1-97.4% and 57.5-100%,
respectively). Only 10 studies analyzed cross-reactions in serum samples from
patients with Chagas disease, and only two studies reported a percentage of
cross-reactivity. In this systematic review, the novel ELISA antigens showed
better sensitivity and specificity with respect to SLA-based ELISAs. However, a
meta-analysis should be performed to confirm this finding.
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