INVESTIGADORES
RUYBAL paula
congresos y reuniones científicas
Título:
Genetic Diversity of Anaplasma marginale in Argentina
Autor/es:
PAULA RUYBAL; ROSALIA MORETTA; ROMINA PETRIGH; ANDRES PEREZ; SILVINA WILCOWSKY; PABLO NUÑEZ; KATHERINE M. KOCAN; JOSÉ DE LA FUENTE; SUSANA TORIONI DE ECHAIDE; MARISA FARBER
Lugar:
Merida, Yucatan , Mexico
Reunión:
Conferencia; 9th Biennial Conference of the Society for Tropical Veterinary Medicine; 2007
Resumen:
Anaplasmosis is a worldwide major constrain in cattle production caused by the
intraerythrocytic rickettsia Anaplasma marginale. This study reports the first
characterization of A. marginale genetic diversity based on the genotype marker
msp1alpha within Argentinean soil and evaluates the influence of Boophilus
microplus infestation. For this purpose, we analyzed whole blood bovine samples
from anaplasmosis outbreaks from B. microplus infested (9 samples) and
eradicated/free (14 samples) regions. Sequence analysis revealed the existence of
15 different genotypes and 31 different repeat units. Twenty of these repeat units
were already reported in a recently published worldwide analysis of this marker with 8
of them only present in Argentina. Moreover, 6 sequences are reported for the first
time in this work. According to tick regions three groups of repeat units were found,
associated to the presence of ticks (20 repeats), to the absence of ticks (6 repeats)
and randomly distributed (5 repeats). Even when sequence M was detected in both
regions it was not randomly distributed as it resulted statistically associated to tick
absence and also presented a specific geographical distribution that empathized this
association. This sequence distribution may collaborate to elucidate A. marginaleAnaplasma marginale. This study reports the first
characterization of A. marginale genetic diversity based on the genotype marker
msp1alpha within Argentinean soil and evaluates the influence of Boophilus
microplus infestation. For this purpose, we analyzed whole blood bovine samples
from anaplasmosis outbreaks from B. microplus infested (9 samples) and
eradicated/free (14 samples) regions. Sequence analysis revealed the existence of
15 different genotypes and 31 different repeat units. Twenty of these repeat units
were already reported in a recently published worldwide analysis of this marker with 8
of them only present in Argentina. Moreover, 6 sequences are reported for the first
time in this work. According to tick regions three groups of repeat units were found,
associated to the presence of ticks (20 repeats), to the absence of ticks (6 repeats)
and randomly distributed (5 repeats). Even when sequence M was detected in both
regions it was not randomly distributed as it resulted statistically associated to tick
absence and also presented a specific geographical distribution that empathized this
association. This sequence distribution may collaborate to elucidate A. marginaleA. marginale genetic diversity based on the genotype marker
msp1alpha within Argentinean soil and evaluates the influence of Boophilus
microplus infestation. For this purpose, we analyzed whole blood bovine samples
from anaplasmosis outbreaks from B. microplus infested (9 samples) and
eradicated/free (14 samples) regions. Sequence analysis revealed the existence of
15 different genotypes and 31 different repeat units. Twenty of these repeat units
were already reported in a recently published worldwide analysis of this marker with 8
of them only present in Argentina. Moreover, 6 sequences are reported for the first
time in this work. According to tick regions three groups of repeat units were found,
associated to the presence of ticks (20 repeats), to the absence of ticks (6 repeats)
and randomly distributed (5 repeats). Even when sequence M was detected in both
regions it was not randomly distributed as it resulted statistically associated to tick
absence and also presented a specific geographical distribution that empathized this
association. This sequence distribution may collaborate to elucidate A. marginaleBoophilus
microplus infestation. For this purpose, we analyzed whole blood bovine samples
from anaplasmosis outbreaks from B. microplus infested (9 samples) and
eradicated/free (14 samples) regions. Sequence analysis revealed the existence of
15 different genotypes and 31 different repeat units. Twenty of these repeat units
were already reported in a recently published worldwide analysis of this marker with 8
of them only present in Argentina. Moreover, 6 sequences are reported for the first
time in this work. According to tick regions three groups of repeat units were found,
associated to the presence of ticks (20 repeats), to the absence of ticks (6 repeats)
and randomly distributed (5 repeats). Even when sequence M was detected in both
regions it was not randomly distributed as it resulted statistically associated to tick
absence and also presented a specific geographical distribution that empathized this
association. This sequence distribution may collaborate to elucidate A. marginaleinfestation. For this purpose, we analyzed whole blood bovine samples
from anaplasmosis outbreaks from B. microplus infested (9 samples) and
eradicated/free (14 samples) regions. Sequence analysis revealed the existence of
15 different genotypes and 31 different repeat units. Twenty of these repeat units
were already reported in a recently published worldwide analysis of this marker with 8
of them only present in Argentina. Moreover, 6 sequences are reported for the first
time in this work. According to tick regions three groups of repeat units were found,
associated to the presence of ticks (20 repeats), to the absence of ticks (6 repeats)
and randomly distributed (5 repeats). Even when sequence M was detected in both
regions it was not randomly distributed as it resulted statistically associated to tick
absence and also presented a specific geographical distribution that empathized this
association. This sequence distribution may collaborate to elucidate A. marginaleB. microplus infested (9 samples) and
eradicated/free (14 samples) regions. Sequence analysis revealed the existence of
15 different genotypes and 31 different repeat units. Twenty of these repeat units
were already reported in a recently published worldwide analysis of this marker with 8
of them only present in Argentina. Moreover, 6 sequences are reported for the first
time in this work. According to tick regions three groups of repeat units were found,
associated to the presence of ticks (20 repeats), to the absence of ticks (6 repeats)
and randomly distributed (5 repeats). Even when sequence M was detected in both
regions it was not randomly distributed as it resulted statistically associated to tick
absence and also presented a specific geographical distribution that empathized this
association. This sequence distribution may collaborate to elucidate A. marginaleA. marginale
flow within Argentinean livestock. Two and even 4 genotypes were found in samples
from highly enzootic area infested with ticks. Moreover, it was previously suggested
that A. marginale strains containing these repeats may have co-evolved with the tick
vector. This strongly support the higher variability observed in Argentinean tick
infested region compared to tick free/eradicated region and suggests an important
role to tick-mediated transmission as significant factor for the generation of genetic
variability of this disease. Finally, 3 of the 31 sequences showed a serine aminoacid
as a new variation at position 20 within the repeat unit. This aminoacid position was
suggested to be important in the rickettsia adhesion to erythrocytes and tick cells,
therefore new adhesion experiments to test the function of this aminoacid in MSP1a
peptides must be done. This work represents the first report of genetic variability of A.
marginale strains in Argentina. Moreover, B. microplus infested and free regions were
analyzed demonstrating a higher variability according to tick influence.
Characterization of A. marginale strains diversity is fundamental to the design of
epidemiological, virulence and vaccine development studies and control strategies for
bovine anaplasmosis.A. marginale strains containing these repeats may have co-evolved with the tick
vector. This strongly support the higher variability observed in Argentinean tick
infested region compared to tick free/eradicated region and suggests an important
role to tick-mediated transmission as significant factor for the generation of genetic
variability of this disease. Finally, 3 of the 31 sequences showed a serine aminoacid
as a new variation at position 20 within the repeat unit. This aminoacid position was
suggested to be important in the rickettsia adhesion to erythrocytes and tick cells,
therefore new adhesion experiments to test the function of this aminoacid in MSP1a
peptides must be done. This work represents the first report of genetic variability of A.
marginale strains in Argentina. Moreover, B. microplus infested and free regions were
analyzed demonstrating a higher variability according to tick influence.
Characterization of A. marginale strains diversity is fundamental to the design of
epidemiological, virulence and vaccine development studies and control strategies for
bovine anaplasmosis.A.
marginale strains in Argentina. Moreover, B. microplus infested and free regions were
analyzed demonstrating a higher variability according to tick influence.
Characterization of A. marginale strains diversity is fundamental to the design of
epidemiological, virulence and vaccine development studies and control strategies for
bovine anaplasmosis.strains in Argentina. Moreover, B. microplus infested and free regions were
analyzed demonstrating a higher variability according to tick influence.
Characterization of A. marginale strains diversity is fundamental to the design of
epidemiological, virulence and vaccine development studies and control strategies for
bovine anaplasmosis.A. marginale strains diversity is fundamental to the design of
epidemiological, virulence and vaccine development studies and control strategies for
bovine anaplasmosis.