TY - JOUR
T1 - Performance of Leishmania PFR1 recombinant antigen in serological diagnosis of asymptomatic canine leishmaniosis by ELISA
AU - Ledesma, D
AU - Berriatua, E
AU - Thomas, MC
AU - Benal, LJ
AU - Papasouliotis, Kostas
AU - Ortuno, M
AU - Tennant, Bryn
AU - Chambers, Julia
AU - Infante, JJ
AU - Lopez, MC
PY - 2017/10/23
Y1 - 2017/10/23
N2 -
Background
Leishmania infantum
is a protozoan parasite transmitted by phlebotomine sand flies that
causes life-threatening disease in humans and dogs. The dog is the
primary reservoir of the parasite and early diagnosis of canine
leishmaniosis is crucial at the clinical and epidemiological level. The
currently available serological tests for CanL diagnostic show
limitations therefore the aim of the present study was to investigate
the diagnostic performance of an indirect antibody ELISA based on the Leishmania infantum recombinant antigen PFR1 in asymptomatically infected dogs. One hundred fifty-six dogs including Leishmania-free
experimental Beagles and pet dogs from England, Scotland and
Leishmania-endemic Murcia in Spain, were tested with the assay. The
later were also tested with two commercial L. infantum crude antigen ELISAs (INgezim and Civtest, respectively) and a real-time kinetoplast PCR test.
Results
Anti-PFR1 antibodies were
detected in the four groups of dogs, and the mean log-transformed
optical density (OD) values were lowest in Beagles and in dogs from
England and highest among dogs from Murcia (p < 0.05).
Using the highest OD in beagles as the PFR1 ELISA cut-off point, the
estimated seroprevalence was 27% (14-40%) in dogs from Murcia, 4% (0-9%)
in dogs from Scotland and 3% (0-8%) in dogs from England (p < 0.05).
Seroprevalence in dogs from Murcia according to the INgezim and Civtest
ELISAs were 24% (12-37%) and 31% (18-45%), respectively, whilst the
prevalence of infection based on PCR in these dogs was 73% (60-86). The
percentages of PFR1-positive dogs that tested negative on the INgezim
and Civtest ELISAs were 30% and 35%, respectively, and all of them
tested positive on the PCR test. Relative to the PCR, the specificity,
sensitivity and area under the ROC curve of the PFR1 ELISA were 100%,
36% and 0.74 (0.63-0.86), respectively.
Conclusions
The ability shown by the PFR1
ELISA to detect infected dogs that go undetected by the crude antigen
ELISAs is clinically and epidemiologically useful and PFR1 could be
considered a candidate for a multi-antigen-based immunoassay for early
detection of L. infantum infected dogs.
AB -
Background
Leishmania infantum
is a protozoan parasite transmitted by phlebotomine sand flies that
causes life-threatening disease in humans and dogs. The dog is the
primary reservoir of the parasite and early diagnosis of canine
leishmaniosis is crucial at the clinical and epidemiological level. The
currently available serological tests for CanL diagnostic show
limitations therefore the aim of the present study was to investigate
the diagnostic performance of an indirect antibody ELISA based on the Leishmania infantum recombinant antigen PFR1 in asymptomatically infected dogs. One hundred fifty-six dogs including Leishmania-free
experimental Beagles and pet dogs from England, Scotland and
Leishmania-endemic Murcia in Spain, were tested with the assay. The
later were also tested with two commercial L. infantum crude antigen ELISAs (INgezim and Civtest, respectively) and a real-time kinetoplast PCR test.
Results
Anti-PFR1 antibodies were
detected in the four groups of dogs, and the mean log-transformed
optical density (OD) values were lowest in Beagles and in dogs from
England and highest among dogs from Murcia (p < 0.05).
Using the highest OD in beagles as the PFR1 ELISA cut-off point, the
estimated seroprevalence was 27% (14-40%) in dogs from Murcia, 4% (0-9%)
in dogs from Scotland and 3% (0-8%) in dogs from England (p < 0.05).
Seroprevalence in dogs from Murcia according to the INgezim and Civtest
ELISAs were 24% (12-37%) and 31% (18-45%), respectively, whilst the
prevalence of infection based on PCR in these dogs was 73% (60-86). The
percentages of PFR1-positive dogs that tested negative on the INgezim
and Civtest ELISAs were 30% and 35%, respectively, and all of them
tested positive on the PCR test. Relative to the PCR, the specificity,
sensitivity and area under the ROC curve of the PFR1 ELISA were 100%,
36% and 0.74 (0.63-0.86), respectively.
Conclusions
The ability shown by the PFR1
ELISA to detect infected dogs that go undetected by the crude antigen
ELISAs is clinically and epidemiologically useful and PFR1 could be
considered a candidate for a multi-antigen-based immunoassay for early
detection of L. infantum infected dogs.
U2 - 10.1186/s12917-017-1224-z
DO - 10.1186/s12917-017-1224-z
M3 - Article (Academic Journal)
C2 - 29061137
SN - 1746-6148
VL - 13
JO - BMC Veterinary Research
JF - BMC Veterinary Research
M1 - 304
ER -