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Peer-reviewed veterinary case report

How marbofloxacin treats Mycoplasma haemofelis in cats with FIV

By Tasker, Séverine et al.·Published in Veterinary microbiology·2006·School of Clinical Veterinary Science, United Kingdom·View original on PubMed

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Original publication title: Effect of chronic FIV infection, and efficacy of marbofloxacin treatment, on Mycoplasma haemofelis infection.

Species:
cat

Plain-English summary

A group of six cats with feline immunodeficiency virus (FIV) and six healthy cats were infected with Mycoplasma haemofelis, a blood parasite that can cause anemia. Some of the cats received marbofloxacin, an antibiotic, while others did not. The treated cats showed a significant decrease in the parasite levels in their blood, although the infection was not completely cleared. This study highlights how FIV-infected cats can still respond to treatment for Mycoplasma haemofelis, but fluctuations in parasite levels can occur.

People also search for: cat FIV treatment · Mycoplasma haemofelis in cats · marbofloxacin for cat infections

Abstract

The purpose of this study was to investigate the effect of chronic feline immunodeficiency virus (FIV) infection, and efficacy of marbofloxacin treatment, on Mycoplasma haemofelis infection. Six cats chronically infected with FIV-Glasgow8 (Group X) and six FIV-free cats (Group Y) were infected with M. haemofelis on Day 0 by intravenous blood inoculation. From Day 0 until Day 86 post-infection (pi), blood samples were collected for M. haemofelis and FIV provirus quantitative real-time PCR and haematology. Three of the six cats in each of Groups X and Y were randomly selected to receive marbofloxacin treatment (2 mg/kg PO q24 h) from Day 16 to 43 pi, with the remaining cats being untreated controls with no antibiotic treatment. The M. haemofelis copy numbers and haematological data were compared between Groups X and Y, and between marbofloxacin-treated and control cats using a Mann-Whitney U-test. M. haemofelis infection was associated with development of macrocytic hypochromic anaemia. In some cats, marked variation in M. haemofelis copy number over time (>100,000-fold difference within 48 h in some cats) and/or cycling of copy number was seen. No correlation was found between FIV provirus copy number and M. haemofelis copy number or haematological variables. No significant effect of chronic FIV infection on M. haemofelis copy number kinetics or haematological changes due to M. haemofelis infection was found, other than MCHC (P=0.03). Marbofloxacin treatment was associated with a significant decrease in M. haemofelis copy number (P=0.002), although consistent clearance of infection was not demonstrated. This study reveals the presence of marked fluctuations in M. haemofelis copy number kinetics in vivo and a significant response to marbofloxacin antibiotic treatment.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/16876338/