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3.
Mem. Inst. Oswaldo Cruz ; 108(6): 772-777, set. 2013. tab, graf
Article in English | LILACS | ID: lil-685482

ABSTRACT

The aims of this study were to characterise the ground-level larval habitats of the mosquito Culex quinquefasciatus, to determine the relationships between habitat characteristics and larval abundance and to examine seasonal larval-stage variations in Córdoba city. Every two weeks for two years, 15 larval habitats (natural and artificial water bodies, including shallow wells, drains, retention ponds, canals and ditches) were visited and sampled for larval mosquitoes. Data regarding the water depth, temperature and pH, permanence, the presence of aquatic vegetation and the density of collected mosquito larvae were recorded. Data on the average air temperatures and accumulated precipitation during the 15 days prior to each sampling date were also obtained. Cx. quinquefasciatus larvae were collected throughout the study period and were generally most abundant in the summer season. Generalised linear mixed models indicated the average air temperature and presence of dicotyledonous aquatic vegetation as variables that served as important predictors of larval densities. Additionally, permanent breeding sites supported high larval densities. In Córdoba city and possibly in other highly populated cities at the same latitude with the same environmental conditions, control programs should focus on permanent larval habitats with aquatic vegetation during the early spring, when the Cx. quinquefasciatus population begins to increase.


Subject(s)
Animals , Animal Distribution/physiology , Culex/growth & development , Ecosystem , Seasons , Magnoliopsida , Argentina , Aquatic Organisms/physiology , Larva , Meteorological Concepts , Mosquito Control/methods , Population Growth , Water/parasitology
4.
Mem. Inst. Oswaldo Cruz ; 108(6): 735-740, set. 2013. tab
Article in English | LILACS | ID: lil-685483

ABSTRACT

Typical human immunodeficiency virus-1 subtype B (HIV-1B) sequences present a GPGR signature at the tip of the variable region 3 (V3) loop; however, unusual motifs harbouring a GWGR signature have also been isolated. Although epidemiological studies have detected this variant in approximately 17-50% of the total infections in Brazil, the prevalence of B"-GWGR in the southernmost region of Brazil is not yet clear. This study aimed to investigate the C2-V3 molecular diversity of the HIV-1B epidemic in southernmost Brazil. HIV-1 seropositive patients were ana-lysed at two distinct time points in the state of Rio Grande do Sul (RS98 and RS08) and at one time point in the state of Santa Catarina (SC08). Phylogenetic analysis classified 46 individuals in the RS98 group as HIV-1B and their molecular signatures were as follows: 26% B"-GWGR, 54% B-GPGR and 20% other motifs. In the RS08 group, HIV-1B was present in 32 samples: 22% B"-GWGR, 59% B-GPGR and 19% other motifs. In the SC08 group, 32 HIV-1B samples were found: 28% B"-GWGR, 59% B-GPGR and 13% other motifs. No association could be established between the HIV-1B V3 signatures and exposure categories in the HIV-1B epidemic in RS. However, B-GPGR seemed to be related to heterosexual individuals in the SC08 group. Our results suggest that the established B"-GWGR epidemics in both cities have similar patterns, which is likely due to their geographical proximity and cultural relationship.


Subject(s)
Female , Humans , Male , HIV Infections/epidemiology , HIV Infections/transmission , HIV Seropositivity/virology , HIV-1 , Amino Acid Motifs , Amino Acid Sequence , Blood Transfusion/adverse effects , Brazil/epidemiology , Drug Users/statistics & numerical data , Heterosexuality , HIV-1 , Homosexuality, Male , Molecular Epidemiology , Phylogeny , Prevalence , Sexual Partners , Sequence Alignment/statistics & numerical data
5.
Mem. Inst. Oswaldo Cruz ; 108(6): 686-690, set. 2013. graf
Article in English | LILACS | ID: lil-685484

ABSTRACT

Recently, while studying erythrocytic apoptosis during Plasmodium yoelii infection, we observed an increase in the levels of non-parasitised red blood cell (nRBC) apoptosis, which could be related to malarial anaemia. Therefore, in the present study, we attempted to investigate whether nRBC apoptosis is associated with the peripheral RBC count, parasite load or immune response. To this end, BALB/c mice were infected with P. yoelii 17XL and nRBC apoptosis, number of peripheral RBCs, parasitaemia and plasmatic levels of cytokines, nitric oxide and anti-RBC antibodies were evaluated at the early and late stages of anaemia. The apoptosis of nRBCs increased at the late stage and was associated with parasitaemia, but not with the intensity of the immune response. The increased percentage of nRBC apoptosis that was observed when anaemia was accentuated was not related to a reduction in peripheral RBCs. We conclude that nRBC apoptosis in P. yoelii malaria appears to be induced in response to a high parasite load. Further studies on malaria models in which acute anaemia develops during low parasitaemia are needed to identify the potential pathogenic role of nRBC apoptosis.


Subject(s)
Animals , Female , Anemia/parasitology , Apoptosis/physiology , Erythrocytes/physiology , Malaria/blood , Plasmodium yoelii , Apoptosis/immunology , Biomarkers , Erythrocyte Count , Erythrocytes/immunology , Flow Cytometry , Interferon-gamma/blood , /blood , /blood , /blood , Mice, Inbred BALB C , Nitric Oxide/blood , Parasite Load , Parasitemia/blood , Statistics, Nonparametric , Tumor Necrosis Factor-alpha/blood
6.
Mem. Inst. Oswaldo Cruz ; 108(6): 755-762, set. 2013. tab, graf
Article in English | LILACS | ID: lil-685485

ABSTRACT

Currently, several assays can confirm acute dengue infection at the point-of-care. However, none of these assays can predict the severity of the disease symptoms. A prognosis test that predicts the likelihood of a dengue patient to develop a severe form of the disease could permit more efficient patient triage and treatment. We hypothesise that mRNA expression of apoptosis and innate immune response-related genes will be differentially regulated during the early stages of dengue and might predict the clinical outcome. Aiming to identify biomarkers for dengue prognosis, we extracted mRNA from the peripheral blood mononuclear cells of mild and severe dengue patients during the febrile stage of the disease to measure the expression levels of selected genes by quantitative polymerase chain reaction. The selected candidate biomarkers were previously identified by our group as differentially expressed in microarray studies. We verified that the mRNA coding for CFD, MAGED1, PSMB9, PRDX4 and FCGR3B were differentially expressed between patients who developed clinical symptoms associated with the mild type of dengue and patients who showed clinical symptoms associated with severe dengue. We suggest that this gene expression panel could putatively serve as biomarkers for the clinical prognosis of dengue haemorrhagic fever.


Subject(s)
Humans , Antigens, Neoplasm/genetics , Cysteine Endopeptidases/genetics , Membrane Glycoproteins/genetics , Neoplasm Proteins/genetics , Peroxiredoxins/genetics , Receptors, IgG/genetics , Receptors, Interleukin-1/genetics , Severity of Illness Index , Severe Dengue/diagnosis , Apoptosis Regulatory Proteins/genetics , Biomarkers , Gene Expression , GPI-Linked Proteins/genetics , Immunity, Innate/genetics , Leukocytes, Mononuclear/immunology , Leukocytes, Mononuclear/pathology , Microarray Analysis , Prognosis , Real-Time Polymerase Chain Reaction , RNA, Messenger/isolation & purification , Serotyping
7.
Mem. Inst. Oswaldo Cruz ; 108(6): 691-698, set. 2013. graf
Article in English | LILACS | ID: lil-685486

ABSTRACT

Acute infection with Trypanosoma cruzi results in intense myocarditis, which progresses to a chronic, asymptomatic indeterminate form. The evolution toward this chronic cardiac form occurs in approximately 30% of all cases of T. cruzi infection. Suppression of delayed type hypersensitivity (DTH) has been proposed as a potential explanation of the indeterminate form. We investigated the effect of cyclophosphamide (CYCL) treatment on the regulatory mechanism of DTH and the participation of heart interstitial dendritic cells (IDCs) in this process using BALB/c mice chronically infected with T. cruzi. One group was treated with CYCL (20 mg/kg body weight) for one month. A DTH skin test was performed by intradermal injection of T. cruzi antigen (3 mg/mL) in the hind-footpad and measured the skin thickness after 24 h, 48 h and 72 h. The skin test revealed increased thickness in antigen-injected footpads, which was more evident in the mice treated with CYCL than in those mice that did not receive treatment. The thickened regions were characterised by perivascular infiltrates and areas of necrosis. Intense lesions of the myocardium were present in three/16 cases and included large areas of necrosis. Morphometric evaluation of lymphocytes showed a predominance of TCD8 cells. Heart IDCs were immunolabelled with specific antibodies (CD11b and CD11c) and T. cruzi antigens were detected using a specific anti-T. cruzi antibody. Identification of T. cruzi antigens, sequestered in these cells using specific anti-T. cruzi antibodies was done, showing a significant increase in the number of these cells in treated mice. These results indicate that IDCs participate in the regulatory mechanisms of DTH response to T. cruzi infection.


Subject(s)
Animals , Chagas Cardiomyopathy/drug therapy , Cyclophosphamide/pharmacology , Dendritic Cells/immunology , Hypersensitivity, Delayed/drug therapy , Immunosuppressive Agents/pharmacology , Trypanosoma cruzi , Antigen Presentation/immunology , Antigens, Protozoan/immunology , Chronic Disease , Chagas Cardiomyopathy/immunology , Hypersensitivity, Delayed/immunology , Mice, Inbred BALB C , Parasitemia/drug therapy , Parasitemia/immunology , Skin Tests
8.
Mem. Inst. Oswaldo Cruz ; 108(6): 741-754, set. 2013. graf
Article in English | LILACS | ID: lil-685487

ABSTRACT

Live attenuated vaccines have recently been introduced for preventing rotavirus disease in children. However, alternative strategies for prevention and treatment of rotavirus infection are needed mainly in developing countries where low vaccine coverage occurs. In the present work, N-acetylcysteine (NAC), ascorbic acid (AA), some nonsteroidal anti-inflammatory drugs (NSAIDs) and peroxisome proliferator-activated receptor gamma (PPARγ) agonists were tested for their ability to interfere with rotavirus ECwt infectivity as detected by the percentage of viral antigen-positive cells of small intestinal villi isolated from ECwt-infected ICR mice. Administration of 6 mg NAC/kg every 8 h for three days following the first diarrhoeal episode reduced viral infectivity by about 90%. Administration of AA, ibuprofen, diclofenac, pioglitazone or rosiglitazone decreased viral infectivity by about 55%, 90%, 35%, 32% and 25%, respectively. ECwt infection of mice increased expression of cyclooxygenase-2, ERp57, Hsc70, NF-κB, Hsp70, protein disulphide isomerase (PDI) and PPARγ in intestinal villus cells. NAC treatment of ECwt-infected mice reduced Hsc70 and PDI expression to levels similar to those observed in villi from uninfected control mice. The present results suggest that the drugs tested in the present work could be assayed in preventing or treating rotaviral diarrhoea in children and young animals.


Subject(s)
Animals , Mice , Acetylcysteine/pharmacology , /pharmacology , Diarrhea/drug therapy , PPAR gamma/agonists , Rotavirus , Rotavirus Infections/drug therapy , Antioxidants/therapeutic use , Cyclooxygenase Inhibitors/therapeutic use , Diarrhea/virology , /metabolism , /metabolism , Intestines/virology , Mice, Inbred ICR , NF-kappa B/metabolism , Protein Disulfide-Isomerases/metabolism
9.
Mem. Inst. Oswaldo Cruz ; 108(6): 730-734, set. 2013. tab, graf
Article in English | LILACS | ID: lil-685488

ABSTRACT

Intrathecal synthesis of human T-lymphotropic virus type 1 (HTLV-1) antibodies (Abs) represents conclusive evidence of a specific immune response in the central nervous system of HTLV-1 associated myelopathy/tropical spastic paraparesis (HAM/TSP) patients. Western blotting (WB) for HTLV Abs in serum is a confirmatory test for HTLV-1 infection. The aim of this study was to standardise the Western blot to demonstrate the intrathecal pattern of Abs against HTLV-1 proteins in HAM/TSP patients. Paired cerebrospinal fluid (CSF) and serum samples were selected from 20 patients with definite HAM/TSP, 19 HTLV-1 seronegative patients and two HTLV-1 patients without definite HAM/TSP. The presence of reactive bands of greater intensity in the CSF compared to serum (or bands in only the CSF) indicated the intrathecal synthesis of anti-HTLV-1 Abs. All definite HAM/TSP patients presented with an intrathecal synthesis of anti-HTLV-1 Abs; these Abs were not detected in the control patients. The most frequent intrathecal targets of anti-HTLV-1 Abs were GD21, rgp46-I and p24 and, to a lesser extent, p19, p26, p28, p32, p36, p53 gp21 and gp46. The intrathecal immune response against env (GD21 and rgp46-I) and gag (p24) proteins represents the most important humoral pattern in HAM/TSP. This response may be used as a diagnostic marker, considering the frequent association of intrathecal anti-HTLV-1 Ab synthesis with HAM/TSP and the pathogenesis of this neurological disease.


Subject(s)
Humans , Antibodies, Viral , Blotting, Western/standards , Central Nervous System/immunology , Human T-lymphotropic virus 1/immunology , Paraparesis, Tropical Spastic/immunology , Antibodies, Viral/blood , Antibodies, Viral/cerebrospinal fluid , Central Nervous System/metabolism , Enzyme-Linked Immunosorbent Assay , Gene Products, env/immunology , Gene Products, gag/immunology , Immunoglobulin G/blood , Immunoglobulin G/cerebrospinal fluid , Paraparesis, Tropical Spastic/blood , Paraparesis, Tropical Spastic/cerebrospinal fluid , Sensitivity and Specificity
10.
Mem. Inst. Oswaldo Cruz ; 108(6): 699-706, set. 2013. tab, graf
Article in English | LILACS | ID: lil-685489

ABSTRACT

Angiostrongylus cantonensis is an important causative agent of eosinophilic meningitis and eosinophilic meningoencephalitis in humans. MicroRNAs (miRNAs) are small non-coding RNAs that participate in a wide range of biological processes. This study employed a deep-sequencing approach to study miRNAs from young adults of A. cantonensis. Based on 16,880,456 high-quality reads, 252 conserved mature miRNAs including 10 antisense miRNAs that belonging to 90 families, together with 10 antisense miRNAs were identified and characterised. Among these sequences, 53 miRNAs from 25 families displayed 50 or more reads. The conserved miRNA families were divided into four groups according to their phylogenetic distribution and a total of nine families without any members showing homology to other nematodes or adult worms were identified. Stem-loop real-time polymerase chain reaction analysis of aca-miR-1-1 and aca-miR-71-1 demonstrated that their level of expression increased dramatically from infective larvae to young adults and then decreased in adult worms, with the male worms exhibiting significantly higher levels of expression than female worms. These findings provide information related to the regulation of gene expression during the growth, development and pathogenesis of young adults of A. cantonensis.


Subject(s)
Animals , Female , Male , Angiostrongylus cantonensis/genetics , High-Throughput Nucleotide Sequencing/methods , MicroRNAs/isolation & purification , Sequence Analysis, RNA/methods , Strongylida Infections/genetics , Angiostrongylus cantonensis/growth & development , Gene Expression Profiling , Gene Expression Regulation, Developmental/genetics , Gene Expression/genetics , Life Cycle Stages/genetics , Phylogeny , Real-Time Polymerase Chain Reaction/methods
11.
Mem. Inst. Oswaldo Cruz ; 108(6): 679-685, set. 2013. graf
Article in English | LILACS | ID: lil-685490

ABSTRACT

Leishmania parasites expose phosphatidylserine (PS) on their surface, a process that has been associated with regulation of host's immune responses. In this study we demonstrate that PS exposure by metacyclic promastigotes of Leishmania amazonensis favours blood coagulation. L. amazonensis accelerates in vitro coagulation of human plasma. In addition, L. amazonensis supports the assembly of the prothrombinase complex, thus promoting thrombin formation. This process was reversed by annexin V which blocks PS binding sites. During blood meal, Lutzomyia longipalpis sandfly inject saliva in the bite site, which has a series of pharmacologically active compounds that inhibit blood coagulation. Since saliva and parasites are co-injected in the host during natural transmission, we evaluated the anticoagulant properties of sandfly saliva in counteracting the procoagulant activity of L. amazonensis . Lu. longipalpis saliva reverses plasma clotting promoted by promastigotes. It also inhibits thrombin formation by the prothrombinase complex assembled either in phosphatidylcholine (PC)/PS vesicles or in L. amazonensis . Sandfly saliva inhibits factor X activation by the intrinsic tenase complex assembled on PC/PS vesicles and blocks factor Xa catalytic activity. Altogether our results show that metacyclic promastigotes of L. amazonensis are procoagulant due to PS exposure. Notably, this effect is efficiently counteracted by sandfly saliva.


Subject(s)
Animals , Humans , Blood Coagulation/physiology , Leishmania/metabolism , Phosphatidylserines/metabolism , Psychodidae/parasitology , Saliva/metabolism , Anticoagulants/metabolism , Cysteine Endopeptidases , Factor V/antagonists & inhibitors , Factor X/antagonists & inhibitors , Factor Xa/antagonists & inhibitors , Insect Vectors/parasitology , Neoplasm Proteins/antagonists & inhibitors , Partial Thromboplastin Time , Phosphatidylcholines/metabolism , Psychodidae/metabolism , Thrombin/antagonists & inhibitors , Tissue Extracts/metabolism
12.
Mem. Inst. Oswaldo Cruz ; 108(6): 718-723, set. 2013. tab
Article in English | LILACS | ID: lil-685491

ABSTRACT

Tuberculosis (TB) is an infectocontagious respiratory disease caused by members of the Mycobacterium tuberculosis complex. A 7 base pair (bp) deletion in the locus polyketide synthase (pks)15/1 is described as polymorphic among members of the M. tuberculosis complex, enabling the identification of Euro-American, Indo-Oceanic and Asian lineages. The aim of this study was to characterise this locus in TB isolates from Mexico. One hundred twenty clinical isolates were recovered from the states of Veracruz and Estado de Mexico. We determined the nucleotide sequence of a ± 400 bp fragment of the locus pks15/1, while genotypic characterisation was performed by spoligotyping. One hundred and fifty isolates contained the 7 bp deletion, while five had the wild type locus. Lineages X (22%), LAM (18%) and T (17%) were the most frequent; only three (2%) of the isolates were identified as Beijing and two (1%) EAI-Manila. The wild type pks15/1 locus was observed in all Asian lineage isolates tested. Our results confirm the utility of locus pks15/1 as a molecular marker for identifying Asian lineages of the M. tuberculosis complex. This marker could be of great value in the epidemiological surveillance of TB, especially in countries like Mexico, where the prevalence of such lineages is unknown.


Subject(s)
Adult , Female , Humans , Male , Middle Aged , Bacterial Proteins/genetics , Genes, Bacterial/genetics , Genetic Loci/genetics , Mycobacterium tuberculosis/genetics , Polyketide Synthases/genetics , Base Sequence , Drug Resistance, Multiple, Bacterial/genetics , Epidemiological Monitoring , Genetic Markers/genetics , Mexico , Mycobacterium tuberculosis/classification , Mycobacterium tuberculosis/isolation & purification , Polymerase Chain Reaction , Sequence Deletion , Sputum/microbiology
13.
Mem. Inst. Oswaldo Cruz ; 108(6): 671-678, set. 2013. tab, graf
Article in English | LILACS | ID: lil-685492

ABSTRACT

Sandflies (Diptera: Psychodidae) are important disease vectors of parasites of the genus Leishmania, as well as bacteria and viruses. Following studies of the midgut transcriptome of Phlebotomus papatasi, the principal vector of Leishmania major, two non-classical Kazal-type serine proteinase inhibitors were identified (PpKzl1 and PpKzl2). Analyses of expression profiles indicated that PpKzl1 and PpKzl2 transcripts are both regulated by blood-feeding in the midgut of P. papatasi and are also expressed in males, larva and pupa. We expressed a recombinant PpKzl2 in a mammalian expression system (CHO-S free style cells) that was applied to in vitro studies to assess serine proteinase inhibition. Recombinant PpKzl2 inhibited α-chymotrypsin to 9.4% residual activity and also inhibited α-thrombin and trypsin to 33.5% and 63.9% residual activity, suggesting that native PpKzl2 is an active serine proteinase inhibitor and likely involved in regulating digestive enzymes in the midgut. Early stages of Leishmania are susceptible to killing by digestive proteinases in the sandfly midgut. Thus, characterising serine proteinase inhibitors may provide new targets and strategies to prevent transmission of Leishmania.


Subject(s)
Animals , Female , Male , Gastrointestinal Tract/enzymology , Insect Vectors/parasitology , Phlebotomus/enzymology , Serine Proteinase Inhibitors/isolation & purification , CHO Cells , Cricetulus , Chymotrypsin/metabolism , Diptera/genetics , Gene Expression , Leishmaniasis/prevention & control , Life Cycle Stages/genetics , Psychodidae/parasitology , Regression Analysis , Reverse Transcriptase Polymerase Chain Reaction , Recombinant Proteins/isolation & purification , Recombinant Proteins/metabolism , Sequence Analysis , Serine Proteinase Inhibitors/genetics , Serine Proteinase Inhibitors/metabolism , Thrombin/metabolism , Trypsin/metabolism
14.
Mem. Inst. Oswaldo Cruz ; 108(6): 763-771, set. 2013. tab, graf
Article in English | LILACS | ID: lil-685493

ABSTRACT

Although the human-landing catch (HLC) method is the most effective for collecting anthropophilic anophelines, it has been increasingly abandoned, primarily for ethical considerations. The objective of the present study was to develop a new trap for the collection of Anopheles darlingi . The initial trials were conducted using the BG-Sentinel trap as a standard for further trap development based on colour, airflow direction and illumination. The performance of the trap was then compared with those of the CDC, Fay-Prince, counterflow geometry trap (CFG) and HLC. All trials were conducted outdoors between 06:00 pm-08:00 pm. Female specimens of An. darlingi were dissected to determine their parity. A total of 8,334 anophelines were captured, of which 4,945 were identified as An. darlingi . The best trap configuration was an all-white version, with an upward airflow and no required light source. This configuration was subsequently named BG-Malaria (BGM). The BGM captured significantly more anophelines than any of the other traps tested and was similar to HLC with respect to the number and parity of anophelines. The BGM trap can be used as an alternative to HLC for collecting anophelines.


Subject(s)
Animals , Female , Anopheles , Insect Vectors , Malaria , Mosquito Control/instrumentation , Carbon Dioxide , Color , Entomology/instrumentation , Odorants , Parity/physiology
15.
Mem. Inst. Oswaldo Cruz ; 108(6): 785-789, set. 2013. tab, graf
Article in English | LILACS | ID: lil-685494

ABSTRACT

Triatoma brasiliensis macromelasoma is revalidated based on the results of previous multidisciplinary studies on the Triatoma brasiliensis complex, consisting of crossing experiments and morphological, biological, ecological and molecular analyses. These taxonomic tools showed the closest relationship between T. b. macromelasoma and Triatoma brasiliensis brasiliensis. T. b. macromelasoma is redescribed based on specimens collected in the type locality and specimens from a F1 colony. The complex now comprises T. b. brasiliensis, T. b. macromelasoma, Triatoma melanica, Triatoma juazeirensis and Triatoma sherlocki. An identification key for all members of the complex is presented. This detailed comparative study of the morphological features of T. b. macromelasoma and the remaining members of the complex corroborates results from multidisciplinary analyses, suggesting that the subspecific status is applicable. This subspecies can be distinguished by the following combination of features: a pronotum with 1+1 narrow brownish-yellow stripes on the submedian carinae, not attaining its apex, hemelytra with membrane cells darkened on the central portion and legs with an incomplete brownish-yellow ring on the apical half of the femora. Because the T. brasiliensis complex is of distinct epidemiological importance throughout its geographic distribution, a precise identification of its five members is important for monitoring and controlling actions against Chagas disease transmission.


Subject(s)
Animals , Female , Male , Triatoma/classification , Insect Vectors/anatomy & histology , Insect Vectors/classification , Reduviidae/anatomy & histology , Reduviidae/classification , Triatoma/anatomy & histology , Triatominae/anatomy & histology , Triatominae/classification
16.
Mem. Inst. Oswaldo Cruz ; 108(6): 790-795, set. 2013. tab, graf
Article in English | LILACS | ID: lil-685495

ABSTRACT

To increase our knowledge of the natural susceptibility of Triatoma infestans to an organophosphate insecticide, we performed toxicological and biochemical studies on three sylvatic populations from Bolivia and two populations from domestic dwellings from Bolivia and Argentina. Fifty-per-cent lethal doses (LD50) were determined based on the topical application of fenitrothion on first instar nymphs and mortality was assessed at 24 h. Both type of populations exhibited LD50ratios significantly higher than 1 with a range of the values (1.42-2.47); the maximum value were found in a sylvatic (-S) population, Veinte de Octubre-S. Samples were biochemically analysed using a glutathione S-transferase activity assay. The highest significant activity was obtained for Veinte de Octubre-S and the lowest activity was obtained for the reference population (102.69 and 54.23 pmol per minute per mg of protein respectively). Two out of the three sylvatic populations (Veinte de Octubre-S and Kirus Mayu-S) exhibited significantly higher glutathione S-transferase activity than that of the reference population. Based on this analysis of the natural susceptibility of this organism to organophosphate insecticides, continental and focal surveys of organophosphate susceptibility should be conducted to evaluate the evolution and distribution of this phenomenon.


Subject(s)
Animals , Fenitrothion , Glutathione Transferase/metabolism , Insecticides , Insecticide Resistance/physiology , Triatoma/drug effects , Bolivia , Housing , Nymph/drug effects , Trees , Triatoma/enzymology
17.
Mem. Inst. Oswaldo Cruz ; 108(6): 724-729, set. 2013. tab, graf
Article in English | LILACS | ID: lil-685496

ABSTRACT

Bacteriocins are antibacterial, proteinaceous substances that mediate microbial dynamics. Bacteriocin production is a highly disseminated property among all major lineages of bacteria, including Shigella. In this paper, we addressed the purification and characterisation of a bacteriocin produced by a Shigella sonnei strain (SS9) isolated from a child with acute diarrhoea. The substance was purified through ammonium-sulphate precipitation and sequential steps of chromatography. The intracellular fraction obtained at 75% ammonium sulphate maintained activity following exposure to pH values from 1-11 and storage at -80ºC for more than two years and was inactivated by high temperatures and proteases. The molecular mass of the purified bacteriocin was determined by mass spectrometry to be 18.56 kDa. The N-terminal sequence of the bacteriocin did not match any other antibacterial proteins described. A putative new bacteriocin produced by S. sonnei has been detected. This bacteriocin may represent a newly described protein or a previously described protein with a newly detected function. Considering that SS9 expresses antagonism against other diarrhoeagenic bacteria, the bacteriocin may contribute to S. sonnei virulence and is potentially applicable to either preventing or controlling diarrhoeal disease.


Subject(s)
Humans , Bacteriocins/isolation & purification , Shigella sonnei/chemistry , Acute Disease , Amino Acid Sequence , Bacteriocins/chemistry , Bacteriocins/metabolism , Chromatography, Reverse-Phase , Diarrhea/microbiology , Mass Spectrometry , Shigella sonnei/growth & development
18.
Mem. Inst. Oswaldo Cruz ; 108(6): 707-717, set. 2013. tab, graf
Article in English | LILACS | ID: lil-685497

ABSTRACT

Schistosomiasis is a major neglected tropical disease caused by trematodes from the genus Schistosoma. Because schistosomes exhibit a complex life cycle and numerous mechanisms for regulating gene expression, it is believed that spliced leader (SL) trans-splicing could play an important role in the biology of these parasites. The purpose of this study was to investigate the function of trans-splicing in Schistosoma mansoni through analysis of genes that may be regulated by this mechanism and via silencing SL-containing transcripts through RNA interference. Here, we report our analysis of SL transcript-enriched cDNA libraries from different S. mansoni life stages. Our results show that the trans-splicing mechanism is apparently not associated with specific genes, subcellular localisations or life stages. In cross-species comparisons, even though the sets of genes that are subject to SL trans-splicing regulation appear to differ between organisms, several commonly shared orthologues were observed. Knockdown of trans-spliced transcripts in sporocysts resulted in a systemic reduction of the expression levels of all tested trans-spliced transcripts; however, the only phenotypic effect observed was diminished larval size. Further studies involving the findings from this work will provide new insights into the role of trans-splicing in the biology of S. mansoni and other organisms. All Expressed Sequence Tags generated in this study were submitted to dbEST as five different libraries. The accessions for each library and for the individual sequences are as follows: (i) adult worms of mixed sexes (LIBEST_027999: JZ139310 - JZ139779), (ii) female adult worms (LIBEST_028000: JZ139780 - JZ140379), (iii) male adult worms (LIBEST_028001: JZ140380 - JZ141002), (iv) eggs (LIBEST_028002: JZ141003 - JZ141497) and (v) schistosomula (LIBEST_028003: JZ141498 - JZ141974).


Subject(s)
Animals , Female , Male , Gene Knockdown Techniques , RNA Precursors/isolation & purification , RNA, Spliced Leader/genetics , Schistosoma mansoni/genetics , Trans-Splicing/physiology , Expressed Sequence Tags , Gene Library , Gene Expression Regulation/genetics , Larva , Life Cycle Stages/genetics , Phenotype , Real-Time Polymerase Chain Reaction , RNA Precursors/genetics , RNA, Double-Stranded , RNA, Small Interfering/metabolism , Schistosoma mansoni/growth & development , Trans-Splicing/genetics
19.
Mem. Inst. Oswaldo Cruz ; 108(6): 778-784, set. 2013. graf
Article in English | LILACS | ID: lil-685498

ABSTRACT

The cuticular hydrocarbons of the Triatoma sordida subcomplex (Hemiptera: Reduviidae: Triatominae) were ana-lysed by gas chromatography and their structures identified by mass spectrometry. They comprised mostly n-alkanes and methyl-branched alkanes with one-four methyl substitutions. n-alkanes consisted of a homologous series from C21-C33 and represented 33-45% of the hydrocarbon fraction; n-C29 was the major component. Methyl-branched alkanes showed alkyl chains from C24-C43. High molecular weight dimethyl and trimethylalkanes (from C35-C39) represented most of the methyl-branched fraction. A few tetramethylalkanes were also detected, comprising mostly even-numbered chains. Several components such as odd-numbered 3-methylalkanes, dimethylalkanes and trimethylalkanes of C37 and C39 showed patterns of variation that allowed the differentiation of the species and populations studied. Triatoma guasayana and Triatoma patagonica showed the most distinct hydrocarbon patterns within the subcomplex. The T. sordida populations from Brazil and Argentina showed significantly different hydrocarbon profiles that posed concerns regarding the homogeneity of the species. Triatoma garciabesi had a more complex hydrocarbon pattern, but it shared some similarity with T. sordida. The quantitative and qualitative variations in the cuticular hydrocarbons may help to elucidate the relationships between species and populations of this insect group.


Subject(s)
Animals , Female , Male , Hydrocarbons/isolation & purification , Lipids/isolation & purification , Triatoma/chemistry , Analysis of Variance , Alkanes/analysis , Gas Chromatography-Mass Spectrometry/methods
20.
Mem. Inst. Oswaldo Cruz ; 108(5): 541-547, ago. 2013. tab, graf
Article in English | LILACS | ID: lil-680760

ABSTRACT

Despite the effectiveness of current hepatitis B virus (HBV) vaccines, it is estimated that 350 million individuals suffer from chronic HBV infection and more than 50% of these affected individuals live on the Asian continent. Panama is a country with a great diversity of foreign groups; the Chinese community is a large example of this phenomenon. There is an urgent need to perform studies that evaluate the prevalence and the genetic diversity of HBV in this community. This study aimed to evaluate the prevalence of HBV and its genotypes and mutant variants in the Chinese population residing in Panama. In total, 320 subjects were enrolled in the study. Forty-two subjects (13.1%) were positive for HBsAg and HBV-DNA from 18 subjects revealed the presence of genotypes B2 and C1. Secondary mutations associated with drug resistance at positions rtV207L and rtN239T of the reverse transcriptase gene were identified. Additionally, the mutation pair A1762T/G1764A was found in three samples and the mutation G1896A was detected in an HBeAg-negative subject. In conclusion, to our knowledge, this is the first study to report high HBV prevalence rates in resident ethnic Chinese in Central America and the presence of genotypes B2 and C1 in this region.


Subject(s)
Adolescent , Adult , Aged , Child , Female , Humans , Male , Middle Aged , Young Adult , Hepatitis B virus/genetics , Hepatitis B/virology , China/ethnology , DNA, Viral/genetics , Genotype , Hepatitis B Surface Antigens/blood , Hepatitis B/ethnology , Hepatitis B/immunology , Mutation , Panama , Sequence Analysis, DNA
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