Clinical and epidemiological data on suspected congenital Zika syndrome (CZS) cases from southern Mato Grosso (MT) in Brazil during the Zika virus (ZIKV) outbreak in 2015-2016 were evaluated. This is a descriptive case series study of newborns whose mothers were suspected cases of ZIKV infections during their pregnancies. The medical records of all the suspected CZS cases (mothers and newborns) treated by the specialized ambulatory service from June 2015 to August 2016 were analyzed. Twenty suspected CZS cases were included in these analyses. They were categorized into four groups based on the clinical and laboratory findings: confirmed cases (n=1), highly probable cases (n=13), moderately probable cases (n=5), and somewhat probable cases (n=1). The mothers tested negative for STORCH (syphilis, toxoplasmosis, other infections, rubella, cytomegalovirus infection, and herpes simplex) and other important congenital infections; however, specific ZIKV tests were not performed during the study period. Microcephaly was observed in the majority of these newborns, and all the patients showed altered cranial computed tomography image findings. Extracranial abnormalities such as arthrogryposis, and otological and ophthalmological manifestations were also observed. Although ZIKV was not confirmed to cause the congenital malformations, this study demonstrated that the clinical and epidemiological findings associated with a STORCH exclusion strengthened the CZS diagnosis. The suspected cases in MT occurred simultaneously with the first CZS cases reported in Brazil, suggesting ZIKV circulation in the study region during the same period.

To provide an overview of hepatitis B infection in Brazil overall, in the South of Brazil, and in the state of Santa Catarina (in southeastern Brazil) for the period of 1996 through 2002, taking into consideration such epidemiological aspects as age and sex. Data were obtained through a literature review and by consulting with Brazil's National Health Foundation and with Santa Catarina's Department of Epidemiological Surveillance. In Brazil, from 1996 through 2000, hepatitis B was the second most prevalent type of viral hepatitis (25%), with hepatitis A leading in terms of the proportion of cases (43%). In Santa Catarina there was a predominance of hepatitis B in relation to other types of hepatitis from 1997 through 2001. In both Brazil and Santa Catarina there was a larger number of cases among males than among females. In terms of age, the highest incidence was found among those 20 to 49 years old in Santa Catarina and among those over 30 for Brazil overall. The South of Brazil was the country's region with the highest incidence of hepatitis B from 1997 through 1999. In Santa Catarina the largest number of cases from 1996 through 2002 occurred in the southern part of the state, followed by the northeastern and far western sections of the state. The number of cases of hepatitis B is still growing in Brazil, and it is important to consider that underreporting may have affected the results described in this study. Throughout Brazil, vaccination should be extended to include adolescents in regions that have a moderate to high incidence of hepatitis B.

Rocio virus (ROCV) caused an outbreak of human encephalitis during the 1970s in Brazil and its immunopathogenesis remains poorly understood. CC-chemokine receptor 5 (CCR5) is a chemokine receptor that binds to macrophage inflammatory protein (MIP-1 α). Both molecules are associated with inflammatory cells migration during infections. In this study, we demonstrated the importance of the CCR5 and MIP-1 α, in the outcome of viral encephalitis of ROCV-infected mice. CCR5 and MIP-1 α knockout mice survived longer than wild-type (WT) ROCV-infected animals. In addition, knockout mice had reduced inflammation in the brain. Assessment of brain viral load showed mice virus detection five days post-infection in wild-type and CCR5−/− mice, while MIP-1 α−/− mice had lower viral loads seven days post-infection. Knockout mice required a higher lethal dose than wild-type mice as well. The CCR5/MIP-1 α axis may contribute to migration of infected cells to the brain and consequently affect the pathogenesis during ROCV infection.