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. 2014 Feb 20;113(4):1499–1503. doi: 10.1007/s00436-014-3792-1

Increased concentration of serum TNF alpha and its correlations with arterial blood pressure and indices of renal damage in dogs infected with Babesia canis

Wojciech Zygner 1,✉, Olga Gójska-Zygner 2, Piotr Bąska 3, Ewa Długosz 1
PMCID: PMC3951886  PMID: 24553975

Abstract

Canine babesiosis is a tick-borne disease caused by parasites of the genus Babesia. Tumour necrosis factor alpha (TNF-α) is a cytokine that plays a role in the pathogenesis of canine babesiosis. In this study, the authors determined the concentration of serum TNF-α in 11 dogs infected with Babesia canis and calculated Spearman’s rank correlations between the concentration of TNF-α and blood pressure, and between TNF-α and indices of renal damage such as: fractional excretion of sodium (FE(Na+)), urinary creatinine to serum creatinine ratio (UCr/SCr), renal failure index (RFI), urine specific gravity (USG) and urinary protein to urinary creatinine ratio (UPC). The results demonstrated statistically significant strong negative correlations between TNF-α and systolic arterial pressure (r = −0.7246), diastolic arterial pressure (r = −0.6642) and mean arterial pressure (r = −0.7151). Serum TNF-α concentration was also statistically significantly correlated with FE(Na+) (r = 0.7056), UCr/SCr (r = −0.8199), USG (r = −0.8075) and duration of the disease (r = 0.6767). The results of this study show there is an increase of serum TNF-α concentration during canine babesiosis, and the increased TNF-α concentration has an influence on the development of hypotension and renal failure in canine babesiosis. This probably results from the fact that TNF-α is involved in the production of nitric oxide and induction of vasodilation and hypotension, which may cause renal ischaemia and hypoxia, and finally acute tubular necrosis and renal failure.

Introduction

Canine babesiosis is a protozoan disease caused by the parasites of the genus Babesia (Matijatko et al. 2012). In Europe, canine babesiosis can be caused by infection with species such as Babesia canis, Babesia vogeli and Babesia gibsoni. Moreover, two species, Babesia felis-like and Babesia microti-like (now considered as Theileria annae), were detected in Germany in dogs imported from Romania, and in Spain, respectively (Hamel et al. 2012; Matijatko et al. 2012). Among these Babesia species, only B. canis has been detected in Poland (Adaszek and Winiarczyk 2011).

Tumour necrosis factor alpha (TNF-α) is a proinflammatory cytokine that plays a significant role in the pathogenesis of babesiosis and malaria, and influences the severity of these diseases (Hemmer et al. 2000; Krause et al. 2007). Complications of canine babesiosis, such as multiple organ dysfunction syndrome and hypotension may result from the parasite, the host or parasite-host interactions (Matijatko et al. 2012). It is probable that TNF-α is involved in the development of hypotension, renal dysfunction and septic shock in canine babesiosis (Matijatko et al. 2009).

Parameters such as fractional excretion of sodium (FE(Na+)), urinary creatinine to serum creatinine ratio (UCr/SCr), renal failure index (RFI), urine specific gravity (USG) and urinary protein to urinary creatinine ratio (UPC) are useful in the differentiation between prerenal and renal azotaemia in azotaemic dogs (Stockham and Scott 2008; Waldrop 2008; Lefebvre 2011).

The purpose of this study was to determine correlations between serum TNF-α concentration and indices of azotaemia (serum urea and creatinine concentration), renal failure indices and blood pressures in dogs infected with B. canis.

Materials and methods

Blood, serum and urine samples were collected from 11 dogs of various breeds (Table 1) infected with B. canis prior to treatment. Diagnosis of infection with B. canis was based on the results of a blood smear examination (Fig. 1) and confirmed by the PCR method described in previous work (Zygner et al. 2012a). Eight clinically healthy dogs were used as a control group. Clinical examination, including blood pressure measurement, was performed during the first visit to the clinic, before sample collection and treatment. Systolic arterial pressure (SAP), diastolic arterial pressure (DAP), mean arterial pressure (MAP) and pulse pressure (PP) were determined using the non-invasive oscillometric technique (Cardell veterinary monitor 9405, Midmark, USA). The concentration of TNF-α in serum samples was determined using an ELISA kit (Quantikine ELISA Canine TNF-α, R&D Systems) and read by an ELISA reader at wavelength 450 nm (MRX Microplate Reader, Dynatech Laboratories) using the program Revelation (version 4.25). Creatinine concentrations (in serum and urine), serum urea concentration and urinary protein concentration were determined by a clinical chemistry analyser (XL 640, Erba Mannheim, Germany). Serum and urinary sodium concentrations were also determined using a clinical chemistry analyser (MEDICA Easy Electrolytes, the Netherlands). Prior to determination of the sodium concentration, urine samples were centrifuged (2,000 rpm, 5 min), then diluted tenfold in deionized water. Urine specific gravity (USG) was determined using a veterinary refractometer (Reichert VET 360, Reichert, USA). The obtained results allowed calculation of indices of renal damage such as FE(Na+), UCr/SCr, RFI and UPC. The FE(Na+) and RFI were calculated using the following formulas: FE(Na+) = UNa × SCr × 100 % ÷ SNa × UCr and RFI = UNa × SCr ÷ UCr, respectively; where UNa is the urinary sodium concentration, SCr is the serum creatinine concentration, SNa is the serum sodium concentration and UCr is the urinary creatinine concentration (Waldrop 2008). The results were analysed using the program Statistica 10. The Mann–Whitney U test was used to compare serum TNF-α concentrations between 8 healthy dogs (group A) and 11 dogs infected with B. canis (group B). Spearman’s rank correlation coefficient was used to calculate correlations between serum TNF-α concentrations in dogs infected with B. canis and their blood pressures (SAP, DAP, MAP and PP), serum urea and creatinine concentrations, FE(Na+), UCr/SCr, RFI USG, UPC and the duration of the disease before admission to the clinic. The value of p < 0.05 was considered significant.

Table 1.

Individual values of serum TNF-α concentrations, blood pressure and renal indices, and clinical signs in 11 dogs with babesiosis

Parameter I II III IV V VI VII VIII IX X XI
TNF-α 20.1 18.7 0 14.7 0 0 27.8 0 26.5 15.5 0
SAP 83 87 120 118 125 121 117 115 70 81 127
DAP 55 44 90 72 87 72 62 60 52 45 86
MAP 74 73 110 103 112 105 99 97 64 69 113
PP 28 43 30 46 38 49 55 55 18 36 41
SCr 4.6 5.1 1.1 1 1 1.2 1.7 1 2.8 3.3 1
SUr 462 264 39 42 38 32 44 44 166 181 42
UCr 52 15.6 161 40 128 281 60 528 75 100 169
UNa 151 168 84 97 65 57 19 108 39 12 71
SNa 141 137 140 137 139 142 146 145 151 146 144
FE(Na+) 9.47 40.09 0.41 1.77 0.36 0.17 3.69 0.14 0.96 0.27 0.29
UCr/SCr 11.3 3.1 146.4 40 128 234.2 35.3 528 26.8 30.3 169
RFI 13.3 54.9 0.6 2.4 0.5 0.2 0.5 0.2 1.5 0.4 1.7
USG 1.013 1.014 1.039 1.060 1.045 1.042 1.005 1.050 1.013 1.016 1.040
UP 160 0 0 520 2250 345 0 1128 3235 820 0
UPC 3.08 0 0 13 17.58 1.23 0 2.14 43.13 8.2 0
DD 4 3 2 1 1 1 2 1 3 2 2
CS An, Ap An, Ap, S, F, Tc, Tp An, Ap, F, V DA, Ap, F, Tc, Tp, DBU An, Ap, F, Tc, Tp, DBU An, Ap, F An, Ap, F, Tc, Tp DA, Ap, F An, Ap, F, DBU An, Ap, F, V An, Ap
DS D, FM, 10y SBD, FM, 7y GSc, M, 6y JRT, M, 3y MBD, FM, 8y MBD, FM, 4y MBD, M, 2y H, FM, 6y GSh, M, 1y GR, FM, 11y MBD, FM, 3y
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I to XI numbering of dogs, TNF-α tumour necrosis factor (in picograms per milliliter), SAP systolic arterial pressure (in millimeters of mercury), DAP diastolic arterial pressure (in millimeters of mercury), MAP mean arterial pressure (in millimeters of mercury), PP pulse pressure (in millimeters of mercury), SCr serum creatinine concentration (in milligrams per deciliter), SUr serum urea concentration (in milligrams per deciliter), UCr urinary creatinine concentration (in milligrams per deciliter), UNa urinary sodium concentration (in milliequivalents per liter), SNa serum sodium concentration (in milliequivalents per liter), FE(Na + ) fractional excretion of sodium (in percent), UCr/SCr urinary creatinine to serum creatinine ratio, RFI renal failure index, USG urine specific gravity, UP urinary protein concentration (in milligrams per deciliter), UPC urinary protein to urinary creatinine ratio, DD duration of the disease (in days), CS clinical signs, DS description of the dog (breed, sex and age in years), An anorexia, Ap apathy, S seizures, F fever, Tc tachycardia, Tp tachypnoea, V vomiting, DA decreased appetite, DBU dark-brown urine, FM female, M male, D Dachshund, SBD St. Bernard dog, GSc Giant Schnauzer, JRT Jack Russell Terrier, MBD mixed breed dog, H Hovawart, GSh German Shepherd, GR Golden Retriever

Fig. 1.

Fig. 1

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Two B. canis merozoites (arrow) within red blood cell observed in blood smear (May-Grünwald-Giemsa staining)

Results

The individual results of 11 dogs infected with B. canis are presented in Table 1. Apathy, anorexia and fever were the most prevalent clinical signs. Detectable concentrations of TNF-α were present in the serum of 6 of the 11 infected dogs. The median serum TNF-α concentration in these dogs amounted to 14.7 pg/mL. Comparison of TNF-α concentrations between groups A and B showed a statistically significantly higher median in infected dogs (Fig. 2). There were statistically significant negative correlations between TNF-α concentration and blood pressures (SAP, DAP and MAP); however, there was no correlation between PP and TNF-α (Table 2). Statistically significant positive correlations were observed between TNF-α concentration and serum urea, serum creatinine and FE(Na+) (Table 2). Statistically significant negative correlations between TNF-α concentrations and UCr/SCr ratio and USG were also observed. There were no statistically significant correlations between TNF-α and RFI or UPC. Duration of the disease was statistically significantly correlated with serum TNF-α concentration (Table 2).

Fig. 2.

Fig. 2

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Comparison of TNF-α concentrations between 8 healthy dogs (group A) and 11 dogs infected with B. canis (group B)

Table 2.

Spearman’s rank correlation between concentration of TNF-α in serum of 11 dogs infected with B. canis and blood pressures, serum urea, creatinine and other renal indices

Correlation r p
TNF-α SAP −0.7246 0.0116*
DAP −0.6642 0.0258*
MAP −0.7151 0.0134*
PP −0.1911 0.5841
SUr 0.7232 0.0119*
SCr 0.7075 0.0149*
FE(Na+) 0.7056 0.0153*
UCr/SCr −0.8199 0.0019*
RFI 0.3927 0.2322
USG −0.8075 0.0026*
UPC 0.1219 0.7209
DD 0.6767 0.0222*
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TNF-α tumour necrosis factor alpha, SAP systolic arterial pressure, DAP diastolic arterial pressure, MAP mean arterial pressure, PP pulse pressure, SUr serum urea concentration, SCr serum creatinine concentration, FE(Na + ) fractional excretion of sodium, UCr/SCr urinary creatinine to serum creatinine ratio, RFI renal failure index, USG urine specific gravity, UPC urinary protein to urinary creatinine ratio, DD duration of the disease (days), r Spearman’s rank correlation coefficient, p a value of p

aStatistically significant result

Discussion

This study showed increased TNF-α concentrations in the sera of dogs infected with B. canis. A similar result has been observed in dogs experimentally infected with Rangelia vitalii, which is a protozoan parasite that causes canine piroplasmosis in Brazil (Da Silva et al. 2013; Paim et al. 2013). Increase of serum TNF-α concentration has also been observed in human and bovine babesiosis (Shaio and Lin 1998; Kontaş and Salmanoğlu 2006).

The authors of this research detected a strong negative correlation between increased serum levels of TNF-α and blood pressure. This may result from the fact that TNF-α is involved in the production of nitric oxide and induction of vasodilation and hypotension (Jacobson et al. 2002; Chauvin et al. 2009). In a previous study, Zygner and Gójska-Zygner (Association between decreased blood pressure and azotaemia in canine babesiosis. Pol J Vet Sci, accepted for publication) showed a negative correlation between blood pressure and the concentration of blood urea and creatinine, as well as lower blood pressure in azotaemic dogs infected with B. canis in comparison to non-azotaemic dogs with canine babesiosis. Thus, it seems probable that the observed strong correlation in this study between serum levels of TNF-α and renal indices such as FE(Na+) and UCr/SCr ratio result from the influences of decreased blood pressure and/or TNF-α on renal failure in canine babesiosis. In previous research, Tracey et al. (1987) showed that injection of dogs with a high dose of TNF-α led to acute tubular necrosis. Increase of the FE(Na+) and RFI and decrease of the UCr/SCr ratio are indicative for acute tubular necrosis (Waldrop 2008); such changes have previously been observed in dogs infected with B. canis (Zygner et al. 2012b, 2013). However, in this study, the RFI was not correlated with TNF-α. This might result from the small group of dogs examined and is an area that requires further research.

The observation in this study of a strong negative correlation between the level of serum TNF-α and USG may also result from an increase in the severity of renal failure, or alternatively, a change from pre-renal azotaemia (higher USG) into renal azotaemia (lower USG) with a concurrent increase of the serum TNF-α concentration. In this work, all azotaemic dogs had relatively low USG (1.013–1.016), but not isosthenuria. One dog had hyposthenuria (USG, <1.008), and serum levels of urea and creatinine were at the upper reference intervals in this dog; thus, it cannot be excluded that azotaemia was developing in this dog. It should also be mentioned that the USG value (decreasing) can be influenced by other factors such as cortisol or aldosterone (Watson 1998); increases in plasma cortisol concentrations have been observed in dogs with canine babesiosis caused by Babesia canis rossi (Schoeman et al. 2007). Moreover, previous work has indicated that the hyponatraemia, hypokalaemia and increased fractional excretions of sodium and potassium observed during canine babesiosis may be connected to an increase of aldosterone during the disease (Adaszek et al. 2012; Zygner et al. 2012a, 2012b).

There was no statistically significant correlation between the TNF-α concentration and UPC in this study. Lobetti and Jacobson (2001) observed a correlation between the value of UPC and severity of babesiosis caused by B. rossi. In theory, UPC is a useful tool in clinical recognition of damage of renal glomeruli when increasing above values of 0.5–1.0 in azotaemic dogs (Stockham and Scott 2008). However, damage of renal glomeruli, although mentioned by Wozniak et al. (1997) in experimentally infected dogs with B. gibsoni, has been rarely observed and mild in dogs with babesiosis (Irwin and Hutchinson 1991; Máthé et al. 2007). In this study, increase of UPC was observed in 7 out of 11 dogs infected with B. canis. However, in these dogs, haemoglobinuria and/or bacteriuria were detected which might influence the protein concentration in urine. The observed lack of correlation between UPC and TNF-α concentration in this research is in agreement (provided decreased blood pressure results from increased TNF-α concentration) with the results of previous work in which a lack of a correlation between UPC and decrease of blood pressure was observed (Buranakarl et al. 2007).

In this work, there were strong positive correlations between serum TNF-α concentration and concentrations of serum urea and creatinine, which suggested that cytokine has an influence on the development of azotaemia in canine babesiosis. Additionally, the correlation between duration of the disease and TNF-α concentration suggested that this cytokine is involved in the development of pre-renal azotaemia, caused by hypotension, at the beginning of the disease and further, is involved in renal azotaemia caused by renal hypoxia when the disease is progressing.

The results of this study show there is an increase in the serum TNF-α concentration in canine babesiosis and that the increased TNF-α concentration influences the development of hypotension and renal failure in canine babesiosis. A previous study has shown that the severity and outcomes of babesiosis in mice experimentally infected with human babesial strains of B. microti and Babesia duncani depend on the host’s immune response and that increased production of TNF-α plays an important role in the pathogenesis of the disease (Hemmer et al. 2000). The results of this work allow us to suppose that this cytokine may also have an influence on the severity of babesiosis in dogs. Further work examining the influence of TNF-α on other complications observed in canine babesiosis are needed to understand the role of this cytokine in the pathogenesis of this disease.

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