Long-term control of Coxiellosis in sheep by annual primary vaccination of gimmers

Coxiella (C.) burnetii, a Gram-negative intracellular bacterium, causes Q fever in humans and Coxiellosis in animals. Ruminants are a primary source of human infection with C.burnetii. In 2013, vaccination was implemented in a sheep flock with 650 ewes associated with two outbreaks of Q fever in hum...

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Veröffentlicht in:Vaccine 2022-08, Vol.40 (35), p.5197-5206
Hauptverfasser: Böttcher, Jens, Bauer, Benjamin U., Ambros, Christina, Alex, Michaela, Domes, Ursula, Roth, Sabine, Boll, Kerstin, Korneli, Martin, Bogner, Karl-Heinz, Randt, Andreas, Janowetz, Britta
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container_end_page 5206
container_issue 35
container_start_page 5197
container_title Vaccine
container_volume 40
creator Böttcher, Jens
Bauer, Benjamin U.
Ambros, Christina
Alex, Michaela
Domes, Ursula
Roth, Sabine
Boll, Kerstin
Korneli, Martin
Bogner, Karl-Heinz
Randt, Andreas
Janowetz, Britta
description Coxiella (C.) burnetii, a Gram-negative intracellular bacterium, causes Q fever in humans and Coxiellosis in animals. Ruminants are a primary source of human infection with C.burnetii. In 2013, vaccination was implemented in a sheep flock with 650 ewes associated with two outbreaks of Q fever in humans in 2008 and 2012. Only gimmers (yearlings) received two doses of a commercial C.burnetii phase I whole cell vaccine three weeks apart (primary vaccination) without any revaccination. Vaginal and nasal swabs collected shortly after lambing were tested by qPCR. Additionally, a group of non-vaccinated sentinels was serologically monitored for phase I (PhI), II (PhII) antibodies and for Interferon γ (IFN-γ) after stimulation of whole blood cells with PhII-antigen with and without an IL-10-neutralizing monoclonal antibody. In 2021, 679 sera collected in 2014–2021 were retested retrospectively with three commercial ELISA kits and one batch of an in-house PhI/PhII-ELISA. A low-level shedding of C.burnetii (
doi_str_mv 10.1016/j.vaccine.2022.07.029
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Ruminants are a primary source of human infection with C.burnetii. In 2013, vaccination was implemented in a sheep flock with 650 ewes associated with two outbreaks of Q fever in humans in 2008 and 2012. Only gimmers (yearlings) received two doses of a commercial C.burnetii phase I whole cell vaccine three weeks apart (primary vaccination) without any revaccination. Vaginal and nasal swabs collected shortly after lambing were tested by qPCR. Additionally, a group of non-vaccinated sentinels was serologically monitored for phase I (PhI), II (PhII) antibodies and for Interferon γ (IFN-γ) after stimulation of whole blood cells with PhII-antigen with and without an IL-10-neutralizing monoclonal antibody. In 2021, 679 sera collected in 2014–2021 were retested retrospectively with three commercial ELISA kits and one batch of an in-house PhI/PhII-ELISA. A low-level shedding of C.burnetii (&lt;103 mean C.burnetii/swab) was observed until 2014. In 2021 C.burnetii was detected in two animals (&lt;103.1C.burnetii/swab), but vaginal swabs collected at two subsequent lambing seasons remained negative. Seroconversion of sentinels was detected until 2017. However, the retrospective analysis of sentinels in 2021 revealed additional single seropositive animals from 2018 to 2021. IFN-γ reactivity was observed during the whole study period; it peaked in 2014 and in 2018 and decreased thereafter. The sporadic detection of C.burnetii and the immune responses of sentinels suggested that a subliminal infection persisted despite vaccination. 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In 2021 C.burnetii was detected in two animals (&lt;103.1C.burnetii/swab), but vaginal swabs collected at two subsequent lambing seasons remained negative. Seroconversion of sentinels was detected until 2017. However, the retrospective analysis of sentinels in 2021 revealed additional single seropositive animals from 2018 to 2021. IFN-γ reactivity was observed during the whole study period; it peaked in 2014 and in 2018 and decreased thereafter. The sporadic detection of C.burnetii and the immune responses of sentinels suggested that a subliminal infection persisted despite vaccination. 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Ruminants are a primary source of human infection with C.burnetii. In 2013, vaccination was implemented in a sheep flock with 650 ewes associated with two outbreaks of Q fever in humans in 2008 and 2012. Only gimmers (yearlings) received two doses of a commercial C.burnetii phase I whole cell vaccine three weeks apart (primary vaccination) without any revaccination. Vaginal and nasal swabs collected shortly after lambing were tested by qPCR. Additionally, a group of non-vaccinated sentinels was serologically monitored for phase I (PhI), II (PhII) antibodies and for Interferon γ (IFN-γ) after stimulation of whole blood cells with PhII-antigen with and without an IL-10-neutralizing monoclonal antibody. In 2021, 679 sera collected in 2014–2021 were retested retrospectively with three commercial ELISA kits and one batch of an in-house PhI/PhII-ELISA. A low-level shedding of C.burnetii (&lt;103 mean C.burnetii/swab) was observed until 2014. 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ispartof Vaccine, 2022-08, Vol.40 (35), p.5197-5206
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source ScienceDirect Journals (5 years ago - present)
subjects Abortion
Animals
Antibodies
Antigens
bacteria
Blood cells
Chronic fatigue syndrome
Coxiella
Farms
flocks
human diseases
Immune response
Immunity
Infections
Interferon
Interleukin 10
Laboratories
Monoclonal antibodies
nose
Outbreaks
Q fever
retrospective studies
Seroconversion
Serology
seroprevalence
Sheep
Vaccination
Vaccines
Vagina
γ-Interferon
title Long-term control of Coxiellosis in sheep by annual primary vaccination of gimmers
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