Amauri Alfieri

Dr. Amauri Alfieri

orcid

Research Focus & Metrics

Academic Career Length

36Years (1991-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 September 1996 in The Journal of Infectious Diseases
Verified
Journal Article
Open access
PDF file
JGJ. R. Gentsch
J. R. Gentsch
PWP. A. Woods
P. A. Woods
MRM. Ramachandran
M. Ramachandran
BDB. K. Das
B. K. Das
JLJ. P. Leite
J. P. Leite
RGR. I. Glass
R. I. Glass
Candidate rotavirus vaccines have been prepared with reassortant strains specifically to protect against the 4 major rotavirus G serotypes (Gl-4). Many studies using P (VP4) genotyping methods have indicated that, worldwide, rotavirus strains of the 4 common G serotypes are each associated with 1 P genotype: Gt, G3, and G4 are associated with P[8], and G2 is associated with P[4]. In contrast, G and P genotyping of rotavirus in specimens from India revealed that a high percentage of the childhood diarrhea strains belong to genotype P[6], and the most common strain had an unusual G serotype, G9. Similarly, in all regions surveyed in Brazil, apparent reassortants of genotype P[8], G5 were found in children with gastroenteritis. These studies indicate that while rotavirus strains have limited diversity in many settings, reassortment between common and uncommon serotypes or animal strains can arise in some settings and, thus, lead to unusual diversity.

23 September 2015 in Transboundary and Emerging Diseases
Verified
Journal Article
Closed access
PDF file
RLR. A. Leme
R. A. Leme
EZE. Zotti
E. Zotti
BAB. K. Alcântara
B. K. Alcântara
MOM. V. Oliveira
M. V. Oliveira
LFL. A. Freitas
L. A. Freitas
AAA. A. Alfieri
A. A. Alfieri

1 October 2006 in Tropical Animal Health and Production
Verified
Journal Article
Closed access
PDF file
MPM. E. Parazzi
M. E. Parazzi
ETE. Takiuchi
E. Takiuchi
KMK. C. Médici
K. C. Médici
AAA. F. Alfieri
A. F. Alfieri

20 February 2018 in Journal of Veterinary Internal Medicine
Verified
Journal Article
Open access
PDF file
GPGiorgio Q. Pereira
Giorgio Q. Pereira
LGLucas Alécio Gomes
Lucas Alécio Gomes
ISIago S. Santos
Iago S. Santos
AAAlice F. Alfieri
Alice F. Alfieri
JWJ. S. Weese
J. S. Weese
MCMarcio Costa
Marcio Costa
Background Diarrhea associated with parvovirus infection is common in dogs. Supportive care is the mainstay of treatment, but recovery may be prolonged and mortality rate can be high. Modification of the intestinal bacterial microbiota has been promising in human and veterinary medicine as an adjunctive treatment of various enteric diseases. Objectives To investigate the safety and efficacy of fecal microbiota transplantation (FMT) on the clinical recovery of puppies with acute hemorrhagic diarrhea syndrome. Animals Sixty‐six puppies with parvovirus infection were evaluated at 2 veterinary hospitals. Methods Randomized clinical trial. Puppies were randomly distributed into 2 groups: standard treatment (STD) and standard treatment + FMT (STD + FMT). The STD puppies (n = 33) received only treatment with IV fluids and antimicrobials and the STD + FMT puppies (n = 33) received FMT in addition to standard treatment. For FMT, 10 g of feces from a healthy dog diluted in 10 mL of saline were administered rectally 6‐12 hours post‐admission. Results Among survivors, treatment with FMT was associated with faster resolution of diarrhea (P < .001) and shorter hospitalization time (P = .001; median, 3 days in STD + FMT; median, 6 days in STD) compared to standard treatment. Mortality in STD was 36.4% (12/33) as compared to 21.2% (7/33) in puppies treated with FMT, but there was no statistical difference between groups (P = .174). Polymerase chain reaction indicated that all animals carried canine parvovirus, strain CPV‐2b. Conclusions Fecal microbiota transplantation in parvovirus‐infected puppies was associated with faster resolution of diarrhea.

3 July 2017 in Viruses
Verified
Journal Article
Open access
PDF file
RLRaquel A. Leme
Raquel A. Leme
AAAlice F. Alfieri
Alice F. Alfieri
AAAmauri Alfieri
Amauri Alfieri
Senecavirus A (SVA) is a positive-sense single-stranded RNA virus that belongs to the Senecavirus genus within the Picornaviridae family. The virus has been silently circulating in pig herds of the USA since 1988. However, cases of senecavirus-associated vesicular disease were reported in Canada in 2007 and in the USA in 2012. Since late 2014 and early 2015, an increasing number of senecavirus outbreaks have been reported in pigs in different producing categories, with this virus being detected in Brazil, China, and Thailand. Considering the novel available data on senecavirus infection and disease, 2015 may be a divisor in the epidemiology of the virus. Among the aspects that reinforce this hypothesis are the geographical distribution of the virus, the affected pig-producing categories, clinical signs associated with the infection, and disease severity. This review presents the current knowledge regarding the senecavirus infection and disease, especially in the last two years. Senecavirus epidemiology, pathogenic potential, host immunological response, diagnosis, and prophylaxis and control measures are addressed. Perspectives are focused on the need for complete evolutionary, epidemiological and pathogenic data and the capability for an immediate diagnosis of senecavirus infection. The health risks inherent in the swine industry cannot be neglected.

1 July 2013 in Journal of Clinical Microbiology
Verified
Journal Article
Closed access
PDF file
MLMichele Lunardi
Michele Lunardi
BABrígida Kussumoto de Alcântara
Brígida Kussumoto de Alcântara
RORodrigo Alejandro Arellano Otonel
Rodrigo Alejandro Arellano Otonel
WRWagner Borges Rodrigues
Wagner Borges Rodrigues
AAAlice Fernandes Alfieri
Alice Fernandes Alfieri
AAAmauri Alfieri
Amauri Alfieri
Equine sarcoids are locally aggressive fibroblastic neoplasms considered to be the most common skin tumors of horses worldwide. Bovine papillomavirus types 1 and 2 have typically been associated with sarcoids in equids. Investigations aiming to identify papillomavirus strains, aside from bovine papillomaviruses 1 and 2, which might be associated with sarcoid lesions, have been lacking. The aim of this article is to report the identification of a third bovine papillomavirus type, bovine papillomavirus 13, associated with equine sarcoids. Six sarcoid lesions were collected from diverse anatomical sites on two horses from southern Brazil. To detect a broad spectrum of papillomavirus strains, eight degenerate primer pairs designed to detect conserved regions on the L1 and E1 genes were tested on the DNA samples. Direct sequencing was then performed on the obtained amplicons, and sequence identities were compared with sequences from all bovine papillomavirus types. The FAP59/FAP64, MY09/MY11, and AR-E1F2/AR-E1R4 sequences generated from the sarcoids were shown to present 99 to 100% identity with bovine papillomavirus 13, a new bovine papillomavirus type previously described in cattle. The results from this study suggest that there is a need to identify bovine papillomavirus type 13 and other papillomavirus strains that might be associated with sarcoids in diverse geographical areas; such investigations might establish the frequency of occurrence of this viral type in these common tumors of equids.