Publications by authors named "Maisa S de Sousa"

To evaluate the effectiveness of a home exercise program called Home Exercise Booklet for People Living with Human T Lymphotropic Virus 1 (HTLV-1). This is a methodological study of content validation with expert judges. A questionnaire with a Likert scale was applied, containing 16 items referring to the content domain.

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Background: Approximately 80% of infected women infected by Chlamydia trachomatis are asymptomatic, although this infection can lead to serious complications in the female reproductive tract. Few data on Chlamydia infection and genotypes are available in Amazonian communities.

Objectives: To describe the prevalence of and associated factors and to identify the genotypes of sexual C.

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Introduction: After three years since the beginning of the pandemic, the new coronavirus continues to raise several questions regarding its infectious process and host response. Several mutations occurred in different regions of the genome, such as in the spike gene, causing the emergence of variants of concern and interest (VOCs and VOIs), of which some present higher transmissibility and virulence, especially among patients with previous comorbidities. It is essential to understand its spread dynamics to prevent and control new biological threats that may occur in the future.

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  • Human T lymphotropic virus 1 (HTLV-1) is linked to inflammatory diseases like HTLV-1-associated myelopathy (HAM), and genetic factors may influence how these diseases develop.
  • The study focuses on a specific genetic variation (rs2232365) in the promoter region of the FOXP3 gene, which is important for regulating immune responses and may affect the severity of inflammatory disorders like HAM.
  • Researchers analyzed DNA samples from asymptomatic carriers, HAM patients, and controls, finding that certain genotypes were associated with higher proviral loads, CD4 T cell counts, and inflammatory markers in those with HAM.
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The human T-lymphotropic virus type 1 (HTLV-1), isolated in 1980, causes T-cell leukemia/lymphoma in adulthood, a type of lymphoproliferative disease, and chronic HTLV-1-associated myelopathy, a disease that causes paralysis of the lower limbs, which occur in about 5% of cases in this viral infection. This study aimed to establish the hematological profile of patients with HTLV-1 infection in Belém do Pará, describing the hematological parameters under study, estimating the frequency of lymphocytic atypical, and associating the hematological profile with diseases and symptoms. Hematologic data from 202 individuals were analyzed, including 87 HTLV-1 infected individuals and 115 non-HTLV-1 infected individuals as a control group, composed, at a great part, of relatives of the infected.

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Background: The Human Papillomavirus (HPV) and Chlamydia trachomatis are the most prevalent Sexually Transmitted Infections (STIs) worldwide, and are associated cervical cancer and pelvic inflammatory disease, respectively. However, 80% of women testing positive are asymptomatic. In the Amazon region, young women, in particular, are widely exposed to the infections and their consequences.

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  • Human T-lymphotropic virus 1 (HTLV-1) is linked to a chronic neurodegenerative disease called HAM/TSP, and the study investigates the role of the anti-inflammatory protein Annexin A1 (AnxA1) in this condition.
  • The research involved 37 HTLV-1 infected individuals, comparing gene expression and plasma levels of AnxA1 among asymptomatic carriers, HAM/TSP patients, and a control group.
  • Findings indicate that while AnxA1 levels were higher in asymptomatic carriers compared to HAM/TSP patients, there are potential prognostic implications suggesting that measuring AnxA1 alongside proviral load could better predict disease progression in HTLV-1 related conditions.
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Background: The forkhead box protein 3 (FOXP3) transcription factor is one of the main markers of immunological suppression in different pathological profiles, and the presence of polymorphic variants may alter the gene expression of this factor. Despite descriptions of an association between the presence of the rs2232365 polymorphism and chronic diseases, the role of the sex variant in this context has not yet been elucidated, as the FOXP3 gene is located on the human sex chromosome X.

Results: To contribute to this topic, 323 women and 373 men were enrolled in the study, of which 101 were diagnosed with chronic viral liver diseases (39 women and 62 men), 67 with HTLV-1 infection (44 women and 23 men), 230 with coronary artery disease (91 women and 139 men) and 298 healthy and uninfected blood donors (149 women and men).

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  • SAMHD1 is a host enzyme that limits the availability of nucleotides for retroviruses like HTLV-1, potentially affecting how infections progress.
  • A study involving 108 HTLV-1 infected individuals examined the impact of genetic variations, specifically polymorphism rs6029941, on infection outcomes, but found no link to susceptibility or symptoms.
  • However, symptomatic patients carrying the G allele had higher levels of viral load and lower IFN-α, suggesting that this polymorphism could contribute to the development of disease symptoms.
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Introduction: Individuals infected with the human T-cell lymphotropic virus type 1 (HTLV-1) commonly present skin lesions, which may be a warning sign for the diagnosis of infection. This study describes the most prevalent skin manifestations in HTLV carriers attended at the clinic of Núcleo de Medicina Tropical (NMT) of the Universidade Federal do Pará (UFPA) in Belém, Pará, Brazil.

Methods: This is a study of a series of cases of patients infected with human T-cell lymphotropic virus types 1 and 2 (HTLV-1/2) treated at NMT UFPA between 1999 and 2016.

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  • Chlamydia trachomatis is the most common bacterial STI globally, with around 80% of infected women showing no symptoms, yet it can cause severe reproductive issues, particularly in rural Amazon regions where data is limited.
  • This study assessed C. trachomatis prevalence among women in the Marajó Archipelago, finding a 4% infection rate, especially in those under 25 and with low income.
  • Key genotypes identified were similar to those seen in urban Brazil, highlighting the need for increased screening and prevention measures in both rural and urban areas to address this overlooked health issue.
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The Human T-cell Lymphotropic Virus (HTLV-1) is a Deltaretrovírus that was first isolated in the 1970s, and associated with Adult T-cell Leucemia-Lymphoma (ATLL), and subsequently to Tropical Spastic Paraparesis-Myelopathy (TSP/HAM). The genetic diversity of the virus varies among geographic regions, although its mutation rate is very low (approximately 1% per thousand years) in comparison with other viruses. The present study determined the genetic diversity of HTLV-1 in the metropolitan region of Belém, in northern Brazil.

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Article Synopsis
  • HTLV-1 infection is linked to adult T-cell leukemia (ATL) and other inflammatory diseases, but it is often overlooked in health discussions.
  • Originally seen as isolated cases, it has been observed that HTLV-1-related diseases can occur in clusters within families, leading to questions about the causes.
  • This study introduces a notable family cluster of HTLV-1 cases spanning three generations, suggesting a possible connection to the FAS -670A/G genetic variation.
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There is only scarce information available on genotypic diversity of the Mycobacterium tuberculosis complex (MTBC) clinical isolates circulating in the Northern part of Brazil, a relatively neglected region regarding research on tuberculosis. We therefore characterized 980 MTBC clinical isolates from the state of Pará, by spoligotyping and data was compared with patterns from around the world, besides analyzing drug susceptibility, and collecting sociodemographic data. We also performed 24 loci MIRU-VNTR typing to evaluate phylogenetic inferences among the East-African-Indian (EAI) lineage strains.

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Background: Human papillomavirus (HPV) infection is associated with cervical cancer, the most frequent cancer in women from northern Brazil. Assessment of the short-term impact of HPV vaccination depends on the availability of data on the prevalence of type-specific HPV in young women in the pre-immunization period, although these data are currently unavailable for the study region. The aim of this study was to estimate the distribution of all mucosal HPV genotypes, including low- and high-risk HPV types, in unvaccinated college students from northern Brazil.

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Background: HTLV-1 is a retrovirus that causes lymphoproliferative disorders and inflammatory and degenerative diseases of the central nervous system in humans. The prevalence of this infection is high in parts of Brazil and there is a general lack of public health care programs. As a consequence, official data on the transmission routes of this virus are scarce.

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Noroviruses are the leading cause of epidemic, non-bacterial outbreaks of acute gastroenteritis, and are also a major cause of sporadic acute gastroenteritis in infants. The aim of the present study was to identify norovirus infections in children not infected by rotavirus admitted to hospital for acute gastroenteritis in Belém. A total of 348 fecal specimens were obtained from children with diarrhea aged less than 5 years, all of whom had tested negative for rotavirus, between May 2008 and April 2010.

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This study utilized the hsp65 polymerase chain reaction restriction analysis (PRA) method in the identification of nontuberculous mycobacteria (NTMs) isolated in a Brazilian mycobacteria laboratory. NTM isolates from clinical specimens collected from 192 patients were characterized using the hsp65 PRA method and analyzed using both 16S rRNA and hsp65 gene sequencing. Only 30% of the NTM strains were correctly identified through PRA, though the suggested inclusion of an additional restriction enzyme could increase the resolution to roughly 90%.

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We isolated 44 strains of rapidly growing mycobacteria (RGM) from 19 patients with pulmonary infections assisted at the Instituto Evandro Chagas (Pará, Brazil) from 2004 to 2007. Identification at the species level was performed by PCR restriction fragment length polymorphism analysis (PRA) of a 441 bp hsp65 fragment and partial 16S rRNA, hsp65, and rpoB gene sequencing. Genotyping by PRA yielded 3 digestion patterns: one identical to Mycobacterium abscessus type I (group I); another to M.

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