Corrigendum to “Physiological and molecular mechanisms associated with cross tolerance between hypoxia and low temperature in Thaumatotibia leucotreta” [J. Insect Physiol. 82 (2015) 75–84]

Corrigendum to “Physiological and molecular mechanisms associated with cross tolerance between hypoxia and low temperature in Thaumatotibia leucotreta” [J. Insect Physiol. 82 (2015) 75–84]

Journal of Insect Physiology 90 (2016) 59–61 Contents lists available at ScienceDirect Journal of Insect Physiology journal homepage: www.elsevier.c...

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Journal of Insect Physiology 90 (2016) 59–61

Contents lists available at ScienceDirect

Journal of Insect Physiology journal homepage: www.elsevier.com/locate/jinsphys

Corrigendum

Corrigendum to ‘‘Physiological and molecular mechanisms associated with cross tolerance between hypoxia and low temperature in Thaumatotibia leucotreta” [J. Insect Physiol. 82 (2015) 75–84] Leigh Boardman a,⇑, Jesper G. Sørensen b, John S. Terblanche a a b

Department of Conservation Ecology and Entomology, Centre for Invasion Biology, Stellenbosch University, Private Bag X1, Matieland 7602, South Africa Section for Genetics, Ecology & Evolution, Department of Bioscience, Aarhus University, Ny Munkegade 116, DK-8000 Aarhus C, Denmark

The authors regret that there was an error in the illustration of the results of the total protein assay, resulting in incorrect representations of this variable in Figs. 2h, 3, Table 2 and Supplementary data in the published version of the paper. These errors have now been corrected and the corrections to the relevant discussion points are noted below. The overall conclusions and outcomes of the study are however unchanged despite this error. Table 2: Mechanical stress, acute hypoxia, chronic dry hypoxia and chronic moist hypoxia pre-treatments increased total protein relative to the handling control at the timepoints indicated. 3.3. Cross tolerance hypothesis: The start of the second paragraph should read: ‘‘More specifically, the non-thermal, non-gas mechanical stress pre-treatment was associated with an increase in total protein concentration, HSP70 and sorbitol (Table 1; Fig. S1h, i, m).” 3.6. Principal components analysis: Factor 1 explains 41.83% of the variance, and factor 2 explains 23.32% (see Fig. 3). According to the revised PCA, total protein did not change in response to low temperatures. The authors would like to apologize for any inconvenience caused. Appendix A. Supplementary data Supplementary data associated with this article can be found, in the online version, at http://dx.doi.org/10.1016/j.jinsphys.2016.05.004.

DOI of original article: http://dx.doi.org/10.1016/j.jinsphys.2015.09.001

⇑ Corresponding author.

E-mail address: [email protected] (L. Boardman). http://dx.doi.org/10.1016/j.jinsphys.2016.05.004 0022-1910/Ó 2016 Elsevier Ltd. All rights reserved.

L. Boardman et al. / Journal of Insect Physiology 90 (2016) 59–61

92 91

0.8 0.6 0.4 0.2 0.0 B

90 SC Mechanical

8.0 a ab

AB

ab AB

ab

6.5

AB b

6.0

B

5.5 5.0 4.5 Handling HC 16

b

(h) b

*

15 14 a

13 12 HC Handling

(k)

3.0 2.5 2.0 1.5 1.0 0.5

1.2 0.8 b

* b

0.0

Median trehalose (μg/mg dry mass)

Median sorbitol (μg/mg dry mass)

(n)

a

0.6 0.4 0.2 0.0 B

X

B b

A

AB AB b

1.0

B

0.9

B

Mechanical SC

5.0

A A

X

Handling HC

(f)

a

ab

1.1

0.8

Mechanical SC

1.2

c

4.5

4.0

A a A

a

3.5

0.8 3.0

0.7 Handling HC

HC Handling

Mechanical SC

*

*

BC

BC

0.21

(i)

A

* *B

0.26

BC C

0.16

**

*

*

0.02 0.01

A a

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0.03

Mechanical SC

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SC Mechanical

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0.11

ab

b

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SC Mechanical

1.6

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ab

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Handling HC

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(m)

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Median glucose (μg/mg dry mass)

Median fructose (μg/mg dry mass)

(j)

ab

1.4

0.31

mass)

Median FA chain length

(g)

Mechanical SC Meantotal totalprotein protein Mean (mg/mlper permg mg thawed (mg/ml thawed …

Body water content (mg/mg lean dry mass)

7.0

1.5

(e)

A A

a

7.5

X

Handling HC

Body lipid content (mg/mg lean dry mass)

HC Handling

(d)

Fat tissue viability

93

(c)

Mean UFA:SFA

94

Silkgland viability

Haemocyte viability (% survival)

1.0

(b)

Median HSP70 expression

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(a)

HC Handling

l) Median maltose (μg/mg dry mass)

60

0.8

SC Mechanical

a

A A

0.6 a

0.4 B

0.2 b

0.0 HC Handling

SC Mechanical

HC Handling

SC Mechanical

HC Handling

SC Mechanical

8 6 4 2 0

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SC Mechanical

Fig. 2. Physiological and biochemical responses to the handling control and mechanical stress pre-treatments: (a) mean haemocyte viability, (b) silk gland viability, (c) fat tissue viability, (d) mean body water content, (e) mean body lipid content, (f) mean UFA:SFA, (g) median fatty acid (FA) chain length, (h) mean total protein concentration, (i) median HSP70 expression, (j–n) median cryoprotectant concentrations of (j) fructose, (k) glucose, (l) maltose, (m) sorbitol and (n) trehalose. Different colours represent the different timepoints (refer to the legend in the bottom right corner, Fig. 1). For tissue viability (b) and (c), data for each timepoint (tB and tX shown as B and X on x-axis) are presented as proportions with the lightest colour indicating tissues with <10% damage (score = 1 on nominal scale) and the darkest colour indicating tissues with >80% damage (score = 3). *denotes a mechanical stress timepoint that was significantly different from the same timepoint in the handling control experiment. Significant differences between timepoints within each experiment are indicated by different letters (small letters for handling control and capital letters for mechanical stress). (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

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L. Boardman et al. / Journal of Insect Physiology 90 (2016) 59–61

Table 2 Significant differences as increase (+) or decrease ( ) relative to the handing control for each of the different pre-treatments – based on least square means from generalized linear models output (Table S5). Timepoints sampled were post pre-treatment (tA), 2 h post pre-treatment (tB), during the standard low temperature exposure (tC), post standard low temperature exposure (tD), 2 h post standard low temperature exposure (tE) and 26 h post standard low temperature exposure (tX). Variablea

Timepoint

Survival

tX

Haemocyte viability

tB tX

Body water content

tA tB tC tD tE tX

Body lipid content

tA tB tC tD tE tX

UFA:SFA

tB tE tX

Fatty acid chain length

tB tE tX

Total protein content

tA tB tC tD tE tX

HSP70

Mechanical stress

High temperature

Acute hypoxia

Chronic dry hypoxia

+

Chronic moist hypoxia +

+ + + + + +

+ + +

+

+

+

+

+

+

+

+ +

+

+

+

+ +

+ + + +

+ +

tA tB tC tD tE tX

Sorbitol

Low temperature +

+

+

+

+

+

+ +

tB tE tX

a Results for pupation, emergence, silk gland viability, fat tissue viability, fructose, glucose, maltose or trehalose were not significantly different to the handling control at any timepoint.

a

b

5 4

1.0

Maltose Glucose

Mechanical stress

Sorbitol

3

Factor 2 : 23.32%

Factor 2: 23.32%

0.5 2 1

Chronic dry hypoxia

Handling control

0 -1 -2

Chronic moist hypoxia

Low temperature

Acute hypoxia High temperature

Fructose

UFA:SFA Trehalose Body water content

Haemocyte viability

Fatty acid chain length 0.0

*Survival

HSP70

Total protein *Emergence

-0.5

Body lipid content *Pupation

-3 -1.0 -4 -5

-4

-3

-2

-1

0

1

Factor 1: 41.83%

2

3

4

5

6

-1.0

-0.5

0.0

0.5

1.0

Factor 1 : 41.83%

Fig. 3. Principal components analysis of mean or median data for all variables measured (except tissue viability) 26 h post standard low temperature exposure (tX) showing the projection for the (a) variables and (b) experiments for the first 2 factors (explaining 65.15% of the variance). Survival, pupation and emergence are plotted in red as supplementary variables, although they had no bearing on the loadings. UFA:SFA – ratio of saturated to unsaturated fatty acids; HSP70 – heat shock protein 70. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)