Molecular survey and genetic diversity of Bartonella spp. in domestic cats from Paraguay

被引:5
|
作者
Sepulveda-Garcia, Paulina [1 ,2 ]
Perez-Macchi, Sandra [3 ]
Goncalves, Luiz Ricardo [4 ]
do Amaral, Renan Bressianini [4 ]
Bittencourt, Pedro [5 ]
Andre, Marcos Rogerio [4 ]
Muller, Ananda [5 ,6 ]
机构
[1] Univ Austral Chile, Fac Ciencias Vet, Inst Med Prevent Vet, Valdivia 5090000, Chile
[2] Univ Austral Chile, Fac Ciencias Vet, Escuela Grad, Valdivia 5090000, Chile
[3] Univ Nacl Asuncion, Fac Ciencias Vet, Dept Clin Vet, Asuncion 001109, Paraguay
[4] Univ Estadual Paulista FCAV UNESP, Fac Ciencias Agr & Vet, Dept Patol Reprod & Saude Unica, BR-14884900 Jaboticabal, SP, Brazil
[5] Ross Univ, One Hlth Ctr Zoonoses & Trop Vet Med, Dept Biomed Sci, Sch Vet Med, Basseterre, St Kitts & Nevi
[6] Univ Austral Chile, Fac Ciencias Vet, Inst Ciencias Clin Vet, Valdivia 5090000, Chile
关键词
B; henselae; clarridgeiae; qPCR; South America; Felids; ARTHROPOD-BORNE PATHOGENS; RIO-DE-JANEIRO; SCRATCH DISEASE; HENSELAE; PREVALENCE; CLARRIDGEIAE; FLEAS; IDENTIFICATION; FELIS; DOGS;
D O I
10.1016/j.meegid.2021.105181
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Although Bartonella spp. is described in cats worldwide, little is known about the occurrence and genetic diversity of Bartonella spp. in cats from South America. To date, it has only been detected in cats from Brazil, Chile and Argentina. This study aimed to undertake a molecular survey and explore the genetic diversity of Bartonella spp. in domestic cats from Paraguay. A TaqMan real-time quantitative PCR (qPCR) targeting the nuoG gene (83 bp) for Bartonella spp. was used to screen 125 blood samples from cats in Asuncion, Paraguay. nuoG qPCRpositive samples were further submitted to conventional PCR assays based on the ITS (453- 717 bp), gltA (767 bp), ftsZ (515 bp), rpoB (333 bp), ribC (585-588 bp), and pap-31 (564 bp) loci. Positive samples were sequenced for species identification, phylogenetic, and haplotype analyses. Bartonella D.N.A. was present in 20.8% (26/125) cat blood samples, with low levels of Bartonella nuoG D.N.A. cPCR products targeting gltA, ftsZ, ITS, and rpoB loci from sixteen cats were successfully sequenced. However, all nouG qPCR-positive samples were negative for the ribC and pap-31 genes. Bartonella henselae [62.5% (10/16)] and Bartonella clarridgeiae [37.5% (6/ 16)] were identified among the sequenced samples. Upon phylogenetic analysis, B. henselae and B. clarridgeiae from Paraguay clustered with sequences detected in domestic and wild cats, dogs, and cat fleas worldwide. Two to four haplotypes of B. henselae and B. clarridgeiae in cats from Paraguay were observed, with some being exclusive and others shared with worldwide distributed haplotypes. Here, we report B. henselae and B. clarridgeiae for the first time in cats from Paraguay. Its circulation in cats suggests the need to consider Bartonellae when testing clinical samples from suspected infectious diseases in humans from Paraguay.
引用
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页数:11
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