Adaptation of < em > gltA < /em > and < em > ssrA < /em > assays for diversity profiling by Illumina sequencing to identify < em > Bartonella henselae, B. clarridgeiae < /em > and < em > B. koehlerae < /em >

Conclusion. The adaptation and multiplexing of existing PCR assays for diversity profiling via NGS is a feasible approach that is superior to traditional Sanger sequencing for Bartonella speciation and resolving mixed Bartonella infections. The adaptation of other PCR primers for Illumina NGS will be useful in future studies where mixed bacterial infections may be present.PMID:34296984 | DOI:10.1099/jmm.0.001400
Source: Journal of Medical Microbiology - Category: Microbiology Authors: Source Type: research