Publications by authors named "Chih-Ling Zao"

To date, there is no clear standard to monitor drug treatment for canine Chagas disease. We used 2 real-time PCR (rtPCR) assays targeting kinetoplast DNA (kDNA) and nuclear satellite DNA (nDNA) to detect in canine whole blood. Samples were collected randomly from 131 untreated dogs with unknown infection status in Texas.

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Objective: To evaluate clinical, serologic, parasitological, and histologic outcomes of dogs with naturally occurring infection treated for 12 months with amiodarone and itraconazole.

Animals: 121 dogs from southern Texas and southern Louisiana.

Procedures: Treatment group dogs (n = 105) received a combination of amiodarone hydrochloride (approx 7.

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A new simian retrovirus (SRV) subtype was discovered in China and the USA from Cambodian-origin cynomolgus monkeys. Histopathological examination from necropsied animals showed multifocal lymphoplasmacystic and histocytic inflammation. The complete genome sequences demonstrated that the US virus isolates were nearly identical (99.

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Article Synopsis
  • Chagas disease, caused by Trypanosoma cruzi, is prevalent in south Texas, posing a risk to outdoor-housed nonhuman primates, particularly cynomolgus macaques, due to exposure to insect vectors and wild mammalian reservoirs.
  • A study found an 8.5% prevalence of T. cruzi in cynomolgus macaques, with 23% of seropositive individuals testing negative for the parasite via real-time PCR, indicating potential discrepancies in diagnostic methods and suggesting infectious stages may not always be visible in tissues.
  • The presence of T. cruzi and associated autoimmune responses could complicate cardiac evaluations in preclinical studies, emphasizing the need for screening outdoor-housed primates
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Fatal Yersinia pseudotuberculosis infection in cynomolgus macaques was diagnosed based upon pathology, microbiology and PCR for this study. Pathological findings included acute, erosive to ulcerative, necrohemorrhagic enterocolitis. Genotyping by PCR showed an O:3 pattern (gmd-fcl(+), ddhC-prt(+), manB(+), ddhA-B(+)), but an additional gene, wbyK, was detected.

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The nature of SRV-4 infection in cynomolgus macaques remains unclear to date. Here, we report the monitoring of 24 cynomolgus monkeys that were naturally infected with SRV-4 for virus isolation, proviral load and antibody. The results indicated that the SRV-4 antibody status was statistically correlated to environmental temperature.

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At least 5 serotypes of exogenous simian retrovirus type D (SRV/D) have been found in nonhuman primates, but only SRV-1, 2 and 3 have been completely sequenced. SRV-4 was recovered once from cynomolgus macaques in California in 1984, but its genome sequences are unknown. Here we report the second identification of SRV-4 and its complete genome from infected cynomolgus macaques with Indochinese and Indonesian/Indochinese mixed ancestry.

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