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The present finding of P. malariae isolates in two chimpanzees reinforces that P. malariae is able to infect chimpanzees as a natural host.
The described assay detected eight of eight and 19 of 19 confirmed HAdV-14a clinical isolates in two separate cohorts from respiratory disease outbreaks.
The combination of MIRU-VNTR with RFLP resulted in the disappearance of two clusters, and a reduction of the number of isolates in two clusters, compared to the clustering observed with IS6110 RFLP clustering alone.
However, the divergence of the closely related isolates in two lineages appears to have occurred more recently, e.g., SD-99-2 and SD-99 4 SD-99 4lineage and the three 2005 isonetes in another.
The PCR multiplex assay was also used to detect carriage isolates in two studies [ 28, 29].
We then determined the relative proportion of southern and northern isolates in two steps.
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The hookworm isolates in three studies were of US origin, as was the roundworm isolate.
The comparative genomics profiling revealed that the genome of B. pertussis Tohama differs from clinical isolates in four regions (RD11 to RD14) [25].
The MexNL-03 sequence differed from the Harris County isolates in three nucleotide positions (0.15% divergence; Table).
At a 60% similarity level, the PFGE clustering analysis revealed a high diversity within the isolates, grouping most of the isolates in three major clusters.
More over, isolates in three of the four subgroups closely clustered with previous identified strains, sharing up high to 97% identity with them.
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