Stool Serology: Development of a Non-Invasive Immunological Method for the Detection of Enterovirus-Specific Antibodies in Congo Gorilla Faeces.

enterovirus faeces gorilla poliovirus specific immunoglobulins

Journal

Microorganisms
ISSN: 2076-2607
Titre abrégé: Microorganisms
Pays: Switzerland
ID NLM: 101625893

Informations de publication

Date de publication:
12 Apr 2021
Historique:
received: 24 03 2021
revised: 07 04 2021
accepted: 09 04 2021
entrez: 30 4 2021
pubmed: 1 5 2021
medline: 1 5 2021
Statut: epublish

Résumé

The incidence of poliovirus has been significantly reduced by as much as 99.9% globally. Alongside this, however, vaccine-associated paralytic poliomyelitis has emerged. Previously, our team reported in the Lésio-Louna-Léfini Nature Reserve (Republic of Congo) the presence of a new In order to assess the potential role of poliovirus infection, we have developed and optimised a protocol, based on the lyophilisation and solubilisation of small volumes of stool extracts from 16 gorilla and 3 humans, to detect specific antibodies by western blot and ELISA. First, total immunoglobulins were detected in the concentrated stool extracts. Specific antibodies were then detected in 4/16 gorilla samples and 2/3 human samples by western blot using both the polio vaccine antigen and the Ibou002 antigen and by ELISA using the polio vaccine antigen. Humoral responses were greater with the Ibou002 antigen. We therefore suggest that this recombinant virus could lead to a polio-like disease in the endangered western lowland gorilla. The development of a non-invasive approach to detect microorganism-specific immunoglobulins from faecal samples opens numerous prospects for application in zoonotic infectious diseases and could revolutionise the screening of animals for important emerging infections, such as Ebola fever, rabies and coronavirus infections.

Sections du résumé

BACKGROUND BACKGROUND
The incidence of poliovirus has been significantly reduced by as much as 99.9% globally. Alongside this, however, vaccine-associated paralytic poliomyelitis has emerged. Previously, our team reported in the Lésio-Louna-Léfini Nature Reserve (Republic of Congo) the presence of a new
METHODS METHODS
In order to assess the potential role of poliovirus infection, we have developed and optimised a protocol, based on the lyophilisation and solubilisation of small volumes of stool extracts from 16 gorilla and 3 humans, to detect specific antibodies by western blot and ELISA.
RESULTS RESULTS
First, total immunoglobulins were detected in the concentrated stool extracts. Specific antibodies were then detected in 4/16 gorilla samples and 2/3 human samples by western blot using both the polio vaccine antigen and the Ibou002 antigen and by ELISA using the polio vaccine antigen. Humoral responses were greater with the Ibou002 antigen.
CONCLUSION CONCLUSIONS
We therefore suggest that this recombinant virus could lead to a polio-like disease in the endangered western lowland gorilla. The development of a non-invasive approach to detect microorganism-specific immunoglobulins from faecal samples opens numerous prospects for application in zoonotic infectious diseases and could revolutionise the screening of animals for important emerging infections, such as Ebola fever, rabies and coronavirus infections.

Identifiants

pubmed: 33921300
pii: microorganisms9040810
doi: 10.3390/microorganisms9040810
pmc: PMC8068960
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Youssouf Sereme (Y)

Institut Hospitalo-Universitaire Méditerranée-Infection, 19-21 Boulevard Jean Moulin, CEDEX 05, 13005 Marseille, France.
Aix-Marseille University, IRD, AP-HM, MEPHI, 13385 Marseille, France.

Sandra Madariaga Zarza (SM)

Institut Hospitalo-Universitaire Méditerranée-Infection, 19-21 Boulevard Jean Moulin, CEDEX 05, 13005 Marseille, France.
Aix-Marseille University, IRD, AP-HM, MEPHI, 13385 Marseille, France.

Hacène Medkour (H)

Institut Hospitalo-Universitaire Méditerranée-Infection, 19-21 Boulevard Jean Moulin, CEDEX 05, 13005 Marseille, France.
Aix-Marseille University, IRD, AP-HM, MEPHI, 13385 Marseille, France.

Inestin Amona (I)

Institut Hospitalo-Universitaire Méditerranée-Infection, 19-21 Boulevard Jean Moulin, CEDEX 05, 13005 Marseille, France.
Aix-Marseille University, IRD, AP-HM, MEPHI, 13385 Marseille, France.
Laboratoire National de Santé Publique, Brazzaville, Congo.
Faculté des Sciences et Techniques, Université Marien NGOUABI, Brazzaville, Congo.

Florence Fenollar (F)

Institut Hospitalo-Universitaire Méditerranée-Infection, 19-21 Boulevard Jean Moulin, CEDEX 05, 13005 Marseille, France.
Aix-Marseille University, IRD, AP-HM, SSA, VITROME, 13385 Marseille, France.

Jean Akiana (J)

Laboratoire National de Santé Publique, Brazzaville, Congo.

Soraya Mezouar (S)

Institut Hospitalo-Universitaire Méditerranée-Infection, 19-21 Boulevard Jean Moulin, CEDEX 05, 13005 Marseille, France.
Aix-Marseille University, IRD, AP-HM, MEPHI, 13385 Marseille, France.

Nicolas Orain (N)

Institut Hospitalo-Universitaire Méditerranée-Infection, 19-21 Boulevard Jean Moulin, CEDEX 05, 13005 Marseille, France.
Aix-Marseille University, IRD, AP-HM, MEPHI, 13385 Marseille, France.

Joana Vitte (J)

Institut Hospitalo-Universitaire Méditerranée-Infection, 19-21 Boulevard Jean Moulin, CEDEX 05, 13005 Marseille, France.
Aix-Marseille University, IRD, AP-HM, MEPHI, 13385 Marseille, France.

Bernard Davoust (B)

Institut Hospitalo-Universitaire Méditerranée-Infection, 19-21 Boulevard Jean Moulin, CEDEX 05, 13005 Marseille, France.
Aix-Marseille University, IRD, AP-HM, MEPHI, 13385 Marseille, France.

Didier Raoult (D)

Institut Hospitalo-Universitaire Méditerranée-Infection, 19-21 Boulevard Jean Moulin, CEDEX 05, 13005 Marseille, France.
Aix-Marseille University, IRD, AP-HM, MEPHI, 13385 Marseille, France.

Oleg Mediannikov (O)

Institut Hospitalo-Universitaire Méditerranée-Infection, 19-21 Boulevard Jean Moulin, CEDEX 05, 13005 Marseille, France.
Aix-Marseille University, IRD, AP-HM, MEPHI, 13385 Marseille, France.

Classifications MeSH