Metagenomic Analysis of Microdissected Valvular Tissue for Etiological Diagnosis of Blood Culture–Negative Endocarditis

Author:

Million Matthieu12,Gaudin Maxime12,Melenotte Cléa12,Chasson Lionel3,Edouard Sophie12,Verdonk Constance4,Prudent Elsa12,Amphoux Bernard12,Meresse Stéphane3,Dorent Richard4,Lepidi Hubert125,La Scola Bernard12,Gorvel Jean-Pierre3,Desnues Christelle126,Raoult Didier12

Affiliation:

1. Institut Hospitalo-Universitaire (IHU) -Méditerranée Infection, Marseille

2. Aix Marseille Univ, Institut de recherche pour le développement (IRD), Assistance Publique Hôpitaux de Marseille, Unité Microbes Evolution Phylogenie et Infections (MEPHI)

3. Aix Marseille Univ, Centre National de la Recherche Scientifique (CNRS), Institut National de la Santé et de la Recherche Médicale (INSERM), Centre d’Immunologie de Marseille-Luminy (CIML)

4. Department of Cardiology, Hôpital Bichat, Assistance Publique - Hôpitaux de Paris (APHP), Paris

5. Service d’anatomie et cytologie pathologique et de neuropathologie, Centre Hospitalo-Universitaire (CHU) Timone, Assistance Publique Hôpitaux de Marseille,, France

6. Aix Marseille Univ, Université de Toulon, Centre National de la Recherche Scientifique (CNRS), Institut de Recherche pour le Développement (IRD), Mediterranean Institute of Oceanography, France

Abstract

Abstract Background Etiological diagnosis is a key to therapeutic adaptation and improved prognosis, particularly for infections such as endocarditis. In blood culture–negative endocarditis (BCNE), 22% of cases remain undiagnosed despite an updated comprehensive syndromic approach. This prompted us to develop a new diagnostic approach. Methods Eleven valves from 10 BCNE patients were analyzed using a method that combines human RNA bait-depletion with phi29 DNA polymerase-based multiple displacement amplification and shotgun DNA sequencing. An additional case in which a microbe was serendipitously visualized by immunofluorescence was analyzed using the same method, but after laser capture microdissection. Results Background DNA prevented any diagnosis in cases analyzed without microdissection because the majority of sequences were contaminants. Moraxella sequences were dramatically enriched in the stained microdissected region of the additional case. A consensus genome sequence of 2.4 Mbp covering more than 94% of the Moraxella osloensis KSH reference genome was reconstructed with 234X average coverage. Several antibiotic-resistance genes were observed. Etiological diagnosis was confirmed using Western blot and specific polymerase chain reaction with sequencing on a different valve sample. Conclusions Microdissection could be a key to the metagenomic diagnosis of infectious diseases when a microbe is visualized but remains unidentified despite an updated optimal approach. Moraxella osloensis should be tested in blood culture–negative endocarditis.

Funder

Agence Nationale de la Recherche

French government

French National Research Agency

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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