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Detection of antibodies in opposition to Chlamydia species in rooster serum


Avian chlamydiosis is a bacterial an infection brought on by Chlamydia micro organism. The at present obtainable checks distinguish Chlamydia species primarily based on genetic materials. Researchers from Wageningen Bioveterinary Analysis (WBVR) developed a take a look at primarily based on antibodies current in animal blood that may decide which Chlamydia species contaminated the animal.

Chlamydia micro organism are gram-negative, intracellular micro organism. The bacterial genus at present consists of fourteen species, every with its personal most popular host. Quite a few these species can’t solely trigger illness of their most popular hosts, but in addition have zoonotic potential. The notorious zoonotic species Chlamydia psittaci has been present in tons of of hen species, together with poultry. This bacterium could cause a extreme type of pneumonia in people, referred to as parrot fever.

Differentiate between species
C. gallinacea and C. psittaci can infect birds, however each species differ in epidemiology and zoonotic potential. It’s due to this fact necessary to have diagnostic instruments which allow detection and distinction between the micro organism species in poultry. The obtainable checks are primarily based on molecular strategies (DNA). These checks solely present details about the present an infection standing of animals, and work if there are sufficient micro organism within the samples taken.

A group of WBVR researchers led by Marloes Heijne and Fimme Jan van der Wal*, investigated whether or not it’s attainable to develop a take a look at to detect antibodies in opposition to Chlamydia species in poultry. Serology is appropriate for monitoring flocks, as antibodies stay current for a very long time after an an infection,” explains Heijne. At current, no differentiating take a look at is out there for Chlamydia serology.”

New take a look at
To allow differentiating serology, a suspension array was designed, with peptides as antigens. These peptides are derived from identified immunoreactive Chlamydia proteins. For almost all of those peptides, species-specific seroreactivity in mammalian sera has been described within the literature. For the suspension array, the peptides had been immobilised on totally different colored spheres, a mixture of which was added to serum to seize the species-specific antibodies. The truth is, a serological suspension array is just like an ELISA. Nevertheless, utilizing the array one can carry out a number of ELISA’s for one pattern concurrently, in a single response. For read-out of the assay we use devoted tools, a Luminex”, Heijne explains. With quite a lot of further measures, the take a look at was made appropriate to be used in a number of animal species. In our research, we confirmed that quite a lot of peptides, which have been used within the literature as antigens for Chlamydia serology in mammals, additionally perform in detecting and differentiating antibodies in opposition to the 2 for poultry necessary Chlamydia species.”

Conclusions
The suspension array can determine antibodies of 4 totally different Chlamydia species in mouse sera. The identical take a look at can also be capable of distinguish between antibodies of C. psittaci and C. gallinacea in rooster sera. As a result of the reactivity of rooster sera was not the identical as that of mice, indicators from rooster sera from the sphere had been tough to interpret. Properly-characterised rooster sera for evaluating the seroreactivity of the peptides are scarce. Nonetheless, outcomes with area sera are according to printed information on the incidence of C. gallinacea in Dutch laying hens. With this, we’ve got demonstrated the proof of idea of differentiating serology for antibodies in opposition to Chlamydia in poultry utilizing peptides in a suspension array.”

* WBVR researcher Fimme Jan van der Wal is first creator of the scientific publication, printed in Veterinary Analysis (2023)54:31

Supply: Wageningen College & Analysis

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