Descloux Elodie, Mediannikov Oleg, Gourinat Ann-Claire, Colot Julien, Chauvet Martine, Mermoud Isabelle, Desoutter Denise, Cazorla Cécile, Klement-Frutos Elise, Antonini Luca, Levasseur Anthony, Bossi Vincent, Davoust Bernard, Merlet Audrey, Goujart Marie-Amélie, Oedin Malik, Brescia Fabrice, Laumond Sylvie, Fournier Pierre-Edouard, Raoult Didier
Service de Médecine Interne et Infectiologie, Centre Hospitalier Territorial Gaston Bourret, Noumea, Nouvelle Calédonie.
Aix Marseille University, Institut pour la recherche et le développement, Assistance Publique-Hôpitaux de Marseille, Microbes, Evolution, Phylogénie et Infection, Institut hospitalo-Universitaire-Méditerranée Infection, Marseille, France.
Clin Infect Dis. 2021 Oct 5;73(7):e1445-e1453. doi: 10.1093/cid/ciaa1648.
Hemotropic mycoplasmas, previously classified in the genus Eperythrozoon, have been reported as causing human infections in Brazil, China, Japan, and Spain.
In 2017, we detected DNA from Candidatus Mycoplasma haemohominis in the blood of a Melanesian patient from New Caledonia presenting with febrile splenomegaly, weight loss, life-threatening autoimmune hemolytic anemia, and hemophagocytosis. The full genome of the bacterium was sequenced from a blood isolate. Subsequently, we retrospectively (2011-2017) and prospectively (2018-2019) tested patients who had been hospitalized with a similar clinico-biological picture. In addition, as these patients had been in contact with frugivorous bats (authorized under conditions for hunting and eating in New Caledonia), we investigated the role of these animals and their biting flies by testing them for hemotropic mycoplasmas.
There were 15 patients found to be infected by this hemotropic mycoplasma. Among them, 4 (27%) died following splenectomy performed either for spontaneous spleen rupture or to cure refractory autoimmune hemolytic anemia. The bacterium was cultivated from the patient's blood. The full genome of the Neocaledonian Candidatus M. haemohominis strain differed from that of a recently identified Japanese strain. Of 40 tested Pteropus bats, 40% were positive; 100% of collected bat flies Cyclopodia horsfieldi (Nycteribiidae, Diptera) were positive. Human, bat, and dipteran strains were highly similar.
The bacterium being widely distributed in bats, Candidatus M. haemohominis, should be regarded as a potential cause of severe infections in humans.
嗜血性支原体以前被归类于附红细胞体属,在巴西、中国、日本和西班牙均有报道可引起人类感染。
2017年,我们在一名来自新喀里多尼亚的美拉尼西亚患者血液中检测到了嗜人无形支原体(Candidatus Mycoplasma haemohominis)的DNA,该患者出现发热性脾肿大、体重减轻、危及生命的自身免疫性溶血性贫血和噬血细胞现象。从血液分离株中对该细菌的全基因组进行了测序。随后,我们对具有相似临床生物学特征的住院患者进行了回顾性研究(2011 - 2017年)和前瞻性研究(2018 - 2019年)。此外,由于这些患者曾接触过食果蝠(在新喀里多尼亚的狩猎和食用条件下是允许的),我们通过检测它们是否感染嗜血性支原体来研究这些动物及其叮咬蝇的作用。
发现有15名患者感染了这种嗜血性支原体。其中,4例(27%)因自发性脾破裂或治疗难治性自身免疫性溶血性贫血而进行脾切除术后死亡。该细菌从患者血液中培养出来。新喀里多尼亚嗜人无形支原体菌株的全基因组与最近鉴定的日本菌株不同。在40只受试的狐蝠中,40%呈阳性;收集的所有蝙蝠蝇霍氏环足蝠(Cyclopodia horsfieldi,蝠蝇科,双翅目)均为100%阳性。人类、蝙蝠和双翅目菌株高度相似。
嗜人无形支原体在蝙蝠中广泛分布,应被视为人类严重感染的潜在病因。